Protein(poly)peptide libraries

[0001] This is a divisional of application Ser. No. 09/025,769 now U.S. Pat. No. 6,300,064, filed Feb. 18, 1998 which is a continuation of PCT/EP96/03647, filed Aug. 19, 1995.

[0002] The present invention relates to synthetic DNA sequences which encode one or more collections of homologous proteins/(poly)peptides, and methods for generating and applying libraries of these DNA sequences. In particular, the invention relates to the preparation of a library of human-derived antibody genes by the use of synthetic consensus sequences which cover the structural repertoire of antibodies encoded in the human genome. Furthermore, the invention relates to the use of a single consensus antibody gene as a universal framework for highly diverse antibody libraries.

[0003] All current recombinant methods which use libraries of proteins/(poly)peptides, e.g. antibodies, to screen for members with desired properties, e.g. binding a given ligand, do not provide the possibility to improve the desired properties of the members in an easy and rapid manner. Usually a library is created either by inserting a random oligonucleotide sequence into one or more DNA sequences cloned from an organism, or a family of DNA sequences is cloned and used as the library. The library is then screened, e.g. using phage display, for members which show the desired property. The sequences of one or more of these resulting molecules are then determined. There is no general procedure available to improve these molecules further on.

[0004] Winter (EP 0 368 684 B1) has provided a method for amplifying (by PCR), cloning, and expressing antibody variable region genes. Starting with these genes he was able to create libraries of functional antibody fragments by randomizing the CDR3 of the heavy and/or the light chain. This process is functionally equivalent to the natural process of VJ and VDJ recombination which occurs during the development of B-cells in the immune system.

[0005] However the Winter invention does not provide a method for optimizing the binding affinities of antibody fragments further on, a process which would be functionally equivalent to the naturally occurring phenomenon of “affinity maturation”, which is provided by the present invention. Furthermore, the Winter invention does not provide for artificial variable region genes, which represent a whole family of structurally similar natural genes, and which can be assembled from synthetic DNA oligonucleotides. Additionally, Winter does not enable the combinatorial assembly of portions of antibody variable regions, a feature which is provided by the present invention. Furthermore, this approach has the disadvantage that the genes of all antibodies obtained in the screening procedure have to be completely sequenced, since, except for the PCR priming regions, no additional sequence information about the library members is available. This is time and labor intensive and potentially leads to sequencing errors.

[0006] The teaching of Winter as well as other approaches have tried to create large antibody libraries having high diversity in the complementarity determining regions (CDRs) as well as in the frameworks to be able to find antibodies against as many different antigens as possible. It has been suggested that a single universal framework may be useful to build antibody libraries, but no approach has yet been successful.

[0007] Another problem lies in the production of reagents derived from antibodies. Small antibody fragments show exciting promise for use as therapeutic agents, diagnostic reagents, and for biochemical research. Thus, they are needed in large amounts, and the expression of antibody fragments, e.g. Fv, single-chain Fv (scFv), or Fab in the periplasm of E. coli (Skerra & Plückthun, 1988; Better et al., 1988) is now used routinely in many laboratories. Expression yields vary widely, however. While some fragments yield up to several mg of functional, soluble protein per liter and OD of culture broth in shake flask culture (Carter et al., 1992, Plückthun et al. 1996), other fragments may almost exclusively lead to insoluble material, often found in so-called inclusion bodies. Functional protein may be obtained from the latter in modest yields by a laborious and time-consuming refolding process. The factors influencing antibody expression levels are still only poorly understood. Folding efficiency and stability of the antibody fragments, protease lability and toxicity of the expressed proteins to the host cells often severely limit actual production levels, and several attempts have been tried to increase expression yields. For example, Knappik & Plückthun (1995) could show that expression yield depends on the antibody sequence. They identified key residues in the antibody framework which influence expression yields dramatically. Similarly, Ullrich et al. (1995) found that point mutations in the CDRs can increase the yields in periplasmic antibody fragment expression. Nevertheless, these strategies are only applicable to a few antibodies. Since the Winter invention uses existing repertoires of antibodies, no influence on expressibility of the genes is possible.

[0008] Furthermore, the findings of Knappik & Plückthun and Ullrich demonstrate that the knowledge about antibodies, especially about folding and expression is still increasing. The Winter invention does not allow to incorporate such improvements into the library design.

[0009] The expressibility of the genes is important for the library quality as well, since the screening procedure relies in most cases on the display of the gene product on a phage surface, and efficient display relies on at least moderate expression of the gene.

[0010] These disadvantages of the existing methodologies are overcome by the present invention, which is applicable for all collections of homologous proteins. It has the following novel and useful features illustrated in the following by antibodies as an example:

[0011] Artificial antibodies and fragments thereof can be constructed based on known antibody sequences, which reflect the structural properties of a whole group of homologous antibody genes. Therefore it is possible to reduce the number of different genes without any loss in the structural repertoire. This approach leads to a limited set of artificial genes, which can be synthesized de novo, thereby allowing introduction of cleavage sites and removing unwanted cleavages sites. Furthermore, this approach enables (i), adapting the codon usage of the genes to that of highly expressed genes in any desired host cell and (ii), analyzing all possible pairs of antibody light (L) and heavy (H) chains in terms of interaction preference, antigen preference or recombinant expression titer, which is virtually impossible using the complete collection of antibody genes of an organism and all combinations thereof.

[0012] The use of a limited set of completely synthetic genes makes it possible to create cleavage sites at the boundaries of encoded structural sub-elements. Therefore, each gene is built up from modules which represent structural sub-elements on the protein/(poly)peptide level. In the case of antibodies, the modules consist of “framework” and “CDR” modules. By creating separate framework and CDR modules, different combinatorial assembly possibilities are enabled. Moreover, if two or more artificial genes carry identical pairs of cleavage sites at the boundaries of each of the genetic sub-elements, pre-built libraries of sub-elements can be inserted in these genes simultaneously, without any additional information related to any particular gene sequence. This strategy enables rapid optimization of, for example, antibody affinity, since DNA cassettes encoding libraries of genetic sub-elements can be (i), pre-built, stored and reused and (ii), inserted in any of these sequences at the right position without knowing the actual sequence or having to determine the sequence of the individual library member.

[0013] Additionally, new information about amino acid residues important for binding, stability, or solubility and expression could be integrated into the library design by replacing existing modules with modules modified according to the new observations.

[0014] The limited number of consensus sequences used for creating the library allows to speed up the identification of binding antibodies after screening. After having identified the underlying consensus gene sequence, which could be done by sequencing or by using fingerprint restriction sites, just those part(s) comprising the random sequence(s) have to be determined. This reduces the probability of sequencing errors and of false-positive results.

[0015] The above mentioned cleavage sites can be used only if they are unique in the vector system where the artificial genes have been inserted. As a result, the vector has to be modified to contain none of these cleavage sites. The construction of a vector consisting of basic elements like resistance gene and origin of replication, where cleavage sites have been removed, is of general interest for many cloning attempts. Additionally, these vector(s) could be part of a kit comprising the above mentioned artificial genes and pre-built libraries.

[0016] The collection of artificial genes can be used for a rapid humanization procedure of non-human antibodies, preferably of rodent antibodies. First, the amino acid sequence of the non-human, preferably rodent antibody is compared with the amino acid sequences encoded by the collection of artificial genes to determine the most homologous light and heavy framework regions. These genes are then used for insertion of the genetic sub-elements encoding the CDRs of the non-human, preferably rodent antibody.

[0017] Surprisingly, it has been found that with a combination of only one consensus sequence for each of the light and heavy chains of a scFv fragment an antibody repertoire could be created yielding antibodies against virtually every antigen. Therefore, one aspect of the present invention is the use of a single consensus sequence as a universal framework for the creation of useful (poly)peptide libraries and antibody consensus sequences useful therefor.

[0018] The present invention enables the creation of useful libraries of (poly)peptides. In a first embodiment, the invention provides for a method of setting up nucleic acid sequences suitable for the creation of said libraries. In a first step, a collection of at least three homologous proteins is identified and then analyzed. Therefore, a database of the protein sequences is established where the protein sequences are aligned to each other. The database is used to define subgroups of protein sequences which show a high degree of similarity in both the sequence and, if information is available, in the structural arrangement. For each of the subgroups a (poly)peptide sequence comprising at least one consensus sequence is deduced which represents the members of this subgroup; the complete collection of (poly)peptide sequences represent therefore the complete structural repertoire of the collection of homologous proteins. These artificial (poly)peptide sequences are then analyzed, if possible, according to their structural properties to identify unfavorable interactions between amino acids within said (poly)peptide sequences or between said or other (poly)peptide sequences, for example, in multimeric proteins. Such interactions are then removed by changing the consensus sequence accordingly. The (poly)peptide sequences are then analyzed to identify sub-elements such as domains, loops, helices or CDRs. The amino acid sequence is backtranslated into a corresponding coding nucleic acid sequence which is adapted to the codon usage of the host planned for expressing said nucleic acid sequences. A set of cleavage sites is set up in a way that each of the sub-sequences encoding the sub-elements identified as described above, is flanked by two sites which do not occur a second time within the nucleic acid sequence. This can be achieved by either identifying a cleavage site already flanking a sub-sequence of by changing one or more nucleotides to create the cleavage site, and by removing that site from the remaining part of the gene. The cleavage sites should be common to all corresponding sub-elements or sub-sequences, thus creating a fully modular arrangement of the sub-sequences in the nucleic acid sequence and of the sub-elements in the corresponding (poly)peptide.

[0019] In a further embodiment, the invention provides for a method which sets up two or more sets of (poly)peptides, where for each set the method as described above is performed, and where the cleavage sites are not only unique within each set but also between any two sets. This method can be applied for the creation of (poly)peptide libraries comprising for example two ex-helical domains from two different proteins, where said library is screened for novel hetero-association domains.

[0020] In yet a further embodiment, at least two of the sets as described above, are derived from the same collection of proteins or at least a part of it. This describes libraries comprising for example, but not limited to, two domains from antibodies such as VH and VL, or two extracellular loops of transmembrane receptors.

[0021] In another embodiment, the nucleic acid sequences set up as described above, are synthesized. This can be achieved by any one of several methods well known to the practitioner skilled in the art, for example, by total gene synthesis or by PCR-based approaches.

[0022] In one embodiment, the nucleic acid sequences are cloned into a vector. The vector could be a sequencing vector, an expression vector or a display (e.g. phage display) vector, which are well known to those skilled in the art. Any vector could comprise one nucleic acid sequence, or two or more nucleic sequences, either in different or the same operon. In the last case, they could either be cloned separately or as contiguous sequences.

[0023] In one embodiment, the removal of unfavorable interactions as described above, leads to enhanced expression of the modified (poly)peptides.

[0024] In a preferred embodiment, one or more sub-sequences of the nucleic acid sequences are replaced by different sequences. This can be achieved by excising the sub-sequences using the conditions suitable for cleaving the cleavage sites adjacent to or at the end of the sub-sequence, for example, by using a restriction enzyme at the corresponding restriction site under the conditions well known to those skilled in the art, and replacing the sub-sequence by a different sequence compatible with the cleaved nucleic acid sequence. In a further preferred embodiment, the different sequences replacing the initial sub-sequence(s) are genomic or rearranged genomic sequences, for example in grafting CDRs from non-human antibodies onto consensus antibody sequences for rapid humanization of non-human antibodies. In the most preferred embodiment, the different sequences are random sequences, thus replacing the sub-sequence by a collection of sequences to introduce variability and to create a library. The random sequences can be assembled in various ways, for example by using a mixture of mononucleotides or preferably a mixture of trinucleotides (Virnekäs et al., 1994) during automated oligonucleotide synthesis, by error-prone PCR or by other methods well known to the practitioner in the art. The random sequences may be completely randomized or biased towards or against certain codons according to the amino acid distribution at certain positions in known protein sequences. Additionally, the collection of random sub-sequences may comprise different numbers of codons, giving rise to a collection of sub-elements having different lengths.

[0025] In another embodiment, the invention provides for the expression of the nucleic acid sequences from a suitable vector and under suitable conditions well known to those skilled in the art.

[0026] In a further preferred embodiment, the (poly)peptides expressed from said nucleic acid sequences are screened and, optionally, optimized. Screening may be performed by using one of the methods well known to the practitioner in the art, such as phage-display, selectively infective phage, polysome technology to screen for binding, assay systems for enzymatic activity or protein stability. (Poly)peptides having the desired property can be identified by sequencing of the corresponding nucleic acid sequence or by amino acid sequencing or mass spectrometry. In the case of subsequent optimization, the nucleic acid sequences encoding the initially selected (poly)peptides can optionally be used without sequencing. Optimization is performed by repeating the replacement of sub-sequences by different sequences, preferably by random sequences, and the screening step one or more times.

[0027] The desired property the (poly)peptides are screened for is preferably, but not exclusively, selected from the group of optimized affinity or specificity for a target molecule, optimized enzymatic activity, optimized expression yields, optimized stability and optimized solubility.

[0028] In one embodiment, the cleavage sites flanking the sub-sequences are sites recognized and cleaved by restriction enzymes, with recognition and cleavage sequences being either identical or different, the restricted sites either having blunt or sticky ends.

[0029] The length of the sub-elements is preferably, but not exclusively ranging between 1 amino acid, such as one residue in the active site of an enzyme or a structure-determining residue, and 150 amino acids, as for whole protein domains. Most preferably, the length ranges between 3 and 25 amino acids, such as most commonly found in CDR loops of antibodies.

[0030] The nucleic acid sequences could be RNA or, preferably, DNA.

[0031] In one embodiment, the (poly)peptides have an amino acid pattern characteristic of a particular species. This can for example be achieved by deducing the consensus sequences from a collection of homologous proteins of just one species, most preferably from a collection of human proteins. Since the (poly)peptides comprising consensus sequences are artificial, they have to be compared to the protein sequence(s) having the closest similarity to ensure the presence of said characteristic amino acid pattern.

[0032] In one embodiment, the invention provides for the creation of libraries of (poly)peptides comprising at least part of members or derivatives of the immunoglobulin superfamily, preferably of member or derivatives of the immunoglobulins. Most preferably, the invention provides for the creation of libraries of human antibodies, wherein said (poly)peptides are or are derived from heavy or light chain variable regions wherein said structural sub-elements are framework regions (FR) 1, 2, 3, or 4 or complementary determining regions (CDR) 1, 2, or 3. In a first step, a database of published antibody sequences of human origin is established where the antibody sequences are aligned to each other. The database is used to define subgroups of antibody sequences which show a high degree of similarity in both the sequence and the canonical fold of CDR loops (as determined by analysis of antibody structures). For each of the subgroups a consensus sequence is deduced which represents the members of this subgroup; the complete collection of consensus sequences represent therefore the complete structural repertoire of human antibodies.

[0033] These artificial genes are then constructed e.g. by total gene synthesis or by the use of synthetic genetic subunits. These genetic subunits correspond to structural sub-elements on the (poly)peptide level. On the DNA level, these genetic subunits are defined by cleavage sites at the start and the end of each of the sub-elements, which are unique in the vector system. All genes which are members of the collection of consensus sequences are constructed such that they contain a similar pattern of corresponding genetic sub-sequences. Most preferably, said (poly)peptides are or are derived from the HuCAL consensus genes: Vκ1, Vκ2, Vκ3, Vκ4, Vλ1, Vλ2, Vλ3, VH1A, VH1B, VH2, VH3, VH4, VH5, VH6, Cκ, Cλ, CH1 or any combination of said HuCAL consensus genes.

[0034] This collection of DNA molecules can then be used to create libraries of antibodies or antibody fragments, preferably Fv, disulphide-linked Fv, single-chain Fv (scFv), or Fab fragments, which may be used as sources of specificities against new target antigens. Moreover, the affinity of the antibodies can be optimized using pre-built library cassettes and a general procedure. The invention provides a method for identifying one or more genes encoding one or more antibody fragments which binds to a target, comprising the steps of expressing the antibody fragments, and then screening them to isolate one or more antibody fragments which bind to a given target molecule. Preferably, an scFv fragment library comprising the combination of HuCAL VH3 and HuCAL Vλ2 consensus genes and at least a random sub-sequence encoding the heavy chain CDR3 sub-element is screened for binding antibodies. If necessary, the modular design of the genes can then be used to excise from the genes encoding the antibody fragments one or more genetic sub-sequences encoding structural sub-elements, and replacing them by one or more second sub-sequences encoding structural sub-elements. The expression and screening steps can then be repeated until an antibody having the desired affinity is generated.

[0035] Particularly preferred is a method in which one or more of the genetic subunits (e.g. the CDRs) are replaced by a random collection of sequences (the library) using the said cleavage sites. Since these cleavage sites are (i) unique in the vector system and (ii) common to all consensus genes, the same (pre-built) library can be inserted into all artificial antibody genes. The resulting library is then screened against any chosen antigen. Binding antibodies are selected, collected and used as starting material for the next library. Here, one or more of the remaining genetic subunits are randomized as described above.

[0036] A further embodiment of the present invention relates to fusion proteins by providing for a DNA sequence which encodes both the (poly)peptide, as described above, as well as an additional moiety. Particularly preferred are moieties which have a useful therapeutic function. For example, the additional moiety may be a toxin molecule which is able to kill cells (Vitetta et al., 1993). There are numerous examples of such toxins, well known to the one skilled in the art, such as the bacterial toxins Pseudomonas exotoxin A, and diphtheria toxin, as well as the plant toxins ricin, abrin, modeccin, saporin, and gelonin. By fusing such a toxin for example to an antibody fragment, the toxin can be targeted to, for example, diseased cells, and thereby have a beneficial therapeutic effect. Alternatively, the additional moiety may be a cytokine, such as IL-2 (Rosenberg & Lotze, 1986), which has a particular effect (in this case a T-cell proliferative effect) on a family of cells. In a further embodiment, the additional moiety may confer on its (poly)peptide partner a means of detection and/or purification. For example, the fusion protein could comprise the modified antibody fragment and an enzyme commonly used for detection purposes, such as alkaline phosphatase (Blake et al., 1984). There are numerous other moieties which can be used as detection or purification tags, which are well known to the practitioner skilled in the art. Particularly preferred are peptides comprising at least five histidine residues (Hochuli et al., 1988), which are able to bind to metal ions, and can therefore be used for the purification of the protein to which they are fused (Lindner et al., 1992). Also provided for by the invention are additional moieties such as the commonly used C-myc and FLAG tags (Hopp et al., 1988; Knappik & Plückthun, 1994).

[0037] By engineering one or more fused additional domains, antibody fragments or any other (poly)peptide can be assembled into larger molecules which also fall under the scope of the present invention. For example, mini-antibodies (Pack, 1994) are dimers comprising two antibody fragments, each fused to a self-associating dimerization domain. Dimerization domains which are particularly preferred include those derived from a leucine zipper (Pack & Plückthun, 1992) or helix-turn-helix motif (Pack et al., 1993).

[0038] All of the above embodiments of the present invention can be effected using standard techniques of molecular biology known to anyone skilled in the art.

[0039] In a further embodiment, the random collection of sub-sequences (the library) is inserted into a singular nucleic acid sequence encoding one (poly)peptide, thus creating a (poly)peptide library based on one universal framework. Preferably a random collection of CDR sub-sequences is inserted into a universal antibody framework, for example into the HuCAL H3κ2 single-chain Fv fragment described above.

[0040] In further embodiments, the invention provides for nucleic acid sequence(s), vector(s) containing the nucleic acid sequence(s), host cell(s) containing the vector(s), and (poly)peptides, obtainable according to the methods described above.

[0041] In a further preferred embodiment, the invention provides for modular vector systems being compatible with the modular nucleic acid sequences encoding the (poly)peptides. The modules of the vectors are flanked by restriction sites unique within the vector system and essentially unique with respect to the restriction sites incorporated into the nucleic acid sequences encoding the (poly)peptides, except for example the restriction sites necessary for cloning the nucleic acid sequences into the vector. The list of vector modules comprises origins of single-stranded replication, origins of double-stranded replication for high- and low copy number plasmids, promotor/operator, repressor or terminator elements, resistance genes, potential recombination sites, gene III for display on filamentous phages, signal sequences, purification and detection tags, and sequences of additional moieties. The vectors are preferably, but not exclusively, expression vectors or vectors suitable for expression and screening of libraries.

[0042] In another embodiment, the invention provides for a kit, comprising one or more of the list of nucleic acid sequence(s), recombinant vector(s), (poly)peptide(s), and vector(s) according to the methods described above, and suitable host cell(s) for producing the (poly)peptide(s).

[0043] In a preferred embodiment, the invention provides for the creation of libraries of human antibodies. In a first step, a database of published antibody sequences of human origin is established. The database is used to define subgroups of antibody sequences which show a high degree of similarity in both the sequence and the canonical fold (as determined by analysis of antibody structures). For each of the subgroups a consensus sequence is deduced which represents the members of this subgroup; the complete collection of consensus sequences represent therefore the complete structural repertoire of human antibodies.

[0044] These artificial genes are then constructed by the use of synthetic genetic subunits. These genetic subunits correspond to structural sub-elements on the protein level. On the DNA level, these genetic subunits are defined by cleavage sites at the start and the end of each of the subelements, which are unique in the vector system. All genes which are members of the collection of consensus sequences are constructed such that they contain a similar pattern of said genetic subunits.

[0045] This collection of DNA molecules can then be used to create libraries of antibodies which may be used as sources of specificities against new target antigens. Moreover, the affinity of the antibodies can be optimised using pre-built library cassettes and a general procedure. The invention provides a method for identifying one or more genes encoding one or more antibody fragments which binds to a target, comprising the steps of expressing the antibody fragments, and then screening them to isolate one or more antibody fragments which bind to a given target molecule. If necessary, the modular design of the genes can then be used to excise from the genes encoding the antibody fragments one or more genetic sub-sequences encoding structural sub-elements, and replacing them by one or more second sub-sequences encoding structural sub-elements. The expression and screening steps can then be repeated until an antibody having the desired affinity is generated.

[0046] Particularly preferred is a method in which one or more of the genetic subunits (e.g. the CDR's) are replaced by a random collection of sequences (the library) using the said cleavage sites. Since these cleavage sites are (i) unique in the vector system and (ii) common to all consensus genes, the same (pre-built) library can be inserted into all artificial antibody genes. The resulting library is then screened against any chosen antigen. Binding antibodies are eluted, collected and used as starting material for the next library. Here, one or more of the remaining genetic subunits are randomised as described above.

Protein:

[0047] The term protein comprises monomeric polypeptide chains as well as homo- or heteromultimeric complexes of two or more polypeptide chains connected either by covalent interactions (such as disulphide bonds) or by non-covalent interactions (such as hydrophobic or electrostatic interactions).

Analysis of Homologous Proteins:

[0048] The amino acid sequences of three or more proteins are aligned to each other (allowing for introduction of gaps) in a way which maximizes the correspondence between identical or similar amino acid residues at all positions. These aligned sequences are termed homologous if the percentage of the sum of identical and/or similar residues exceeds a defined threshold. This threshold is commonly regarded by those skilled in the art as being exceeded when at least 15% of the amino acids in the aligned genes are identical, and at least 30% are similar. Examples for families of homologous proteins are: immunoglobulin superfamily, scavenger receptor superfamily, fibronectin superfamilies (e.g. type II and III), complement control protein superfamily, cytokine receptor superfamily, cystine knot proteins, tyrosine kinases, and numerous other examples well known to one of ordinary skill in the art.

Consensus Sequence:

[0049] Using a matrix of at least three aligned amino acid sequences, and allowing for gaps in the alignment, it is possible to determine the most frequent amino acid residue at each position. The consensus sequence is that sequence which comprises the amino acids which are most frequently represented at each position. In the event that two or more amino acids are equally represented at a single position, the consensus sequence includes both or all of those amino acids.

Removing Unfavorable Interactions:

[0050] The consensus sequence is per se in most cases artificial and has to be analyzed in order to change amino acid residues which, for example, would prevent the resulting molecule to adapt a functional tertiary structure or which would block the interaction with other (poly)peptide chains in multimeric complexes. This can be done either by (i) building a three-dimensional model of the consensus sequence using known related structures as a template, and identifying amino acid residues within the model which may interact unfavorably with each other, or (ii) analyzing the matrix of aligned amino acid sequences in order to detect combinations of amino acid residues within the sequences which frequently occur together in one sequence and are therefore likely to interact with each other. These probable interaction-pairs are then tabulated and the consensus is compared with these “interaction maps”. Missing or wrong interactions in the consensus are repaired accordingly by introducing appropriate changes in amino acids which minimize unfavorable interactions.

Identification of Structural Sub-Elements:

[0051] Structural sub-elements are stretches of amino acid residues within a protein/(poly)peptide which correspond to a defined structural or functional part of the molecule. These can be loops (e.g. CDR loops of an antibody) or any other secondary or functional structure within the protein/(poly)peptide (domains, α-helices, β-sheets, framework regions of antibodies, etc.). A structural sub-element can be identified using known structures of similar or homologous (poly)peptides, or by using the above mentioned matrices of aligned amino acid sequences. Here the variability at each position is the basis for determining stretches of amino acid residues which belong to a structural sub-element (e.g. hypervariable regions of an antibody).

Sub-Sequence:

[0052] A sub-sequence is defined as a genetic module which is flanked by unique cleavage sites and encodes at least one structural sub-element. It is not necessarily identical to a structural sub-element.

Cleavage Site:

[0053] A short DNA sequence which is used as a specific target for a reagent which cleaves DNA in a sequence-specific manner (e.g. restriction endonucleases).

Compatible Cleavage Sites:

[0054] Cleavage sites are compatible with each other, if they can be efficiently ligated without modification and, preferably, also without adding an adapter molecule.

Unique Cleavage Sites:

[0055] A cleavage site is defined as unique if it occurs only once in a vector containing at least one of the genes of interest, or if a vector containing at least one of the genes of interest could be treated in a way that only one of the cleavage sites could be used by the cleaving agent.

Corresponding (Poly)Peptide Sequences:

[0056] Sequences deduced from the same part of one group of homologous proteins are called corresponding (poly)peptide sequences.

Common Cleavage Sites:

[0057] A cleavage site in at least two corresponding sequences, which occurs at the same functional position (i.e. which flanks a defined sub-sequence), which can be hydrolyzed by the same cleavage tool and which yields identical compatible ends is termed a common cleavage site.

Excising Genetic Sub-Sequences:

[0058] A method which uses the unique cleavage sites and the corresponding cleavage reagents to cleave the target DNA at the specified positions in order to isolate, remove or replace the genetic sub-sequence flanked by these unique cleavage sites.

Exchanging Genetic Sub-Sequences:

[0059] A method by which an existing sub-sequence is removed using the flanking cleavage sites of this sub-sequence, and a new sub-sequence or a collection of sub-sequences, which contain ends compatible with the cleavage sites thus created, is inserted.

Expression of Genes:

[0060] The term expression refers to in vivo or in vitro processes, by which the information of a gene is transcribed into mRNA and then translated into a protein/(poly)peptide. Thus, the term expression refers to a process which occurs inside cells, by which the information of a gene is transcribed into mRNA and then into a protein. The term expression also includes all events of post-translational modification and transport, which are necessary for the (poly)peptide to be functional.

Screening of Protein (Poly)Peptide Libraries:

[0061] Any method which allows isolation of one or more proteins/(poly)peptides having a desired property from other proteins/(poly)peptides within a library.

Amino Acid Pattern Characteristic for a Species:

[0062] A (poly)peptide sequence is assumed to exhibit an amino acid pattern characteristic for a species if it is deduced from a collection of homologous proteins from just this species.

Immunoglobulin Superfamily (IgSF):

[0063] The IgSF is a family of proteins comprising domains being characterized by the immunoglobulin fold. The IgSF comprises for example T-cell receptors and the immunoglobulins (antibodies).

Antibody Framework:

[0064] A framework of an antibody variable domain is defined by Kabat et al. (1991) as the part of the variable domain which serves as a scaffold for the antigen binding loops of this variable domain.

Antibody CDR:

[0065] The CDRs (complementarity determining regions) of an antibody consist of the antigen binding loops, as defined by Kabat et al. (1991). Each of the two variable domains of an antibody Fv fragment contain three CDRs.

HuCAL:

[0066] Acronym for Human Combinatorial Antibody Library. Antibody Library based on modular consensus genes according to the invention (see Example 1).

Antibody Fragment:

[0067] Any portion of an antibody which has a particular function, e.g. binding of antigen. Usually, antibody fragments are smaller than whole antibodies. Examples are Fv, disulphide-linked Fv, single-chain Fv (scFv), or Fab fragments. Additionally, antibody fragments are often engineered to include new functions or properties.

Universal Framework:

[0068] One single framework which can be used to create the full variability of functions, specificities or properties which is originally sustained by a large collection of different frameworks, is called universal framework.

Binding of an Antibody to its Target:

[0069] The process which leads to a tight and specific association between an antibody and a corresponding molecule or ligand is called binding. A molecule or ligand or any part of a molecule or ligand which is recognized by an antibody is called the target.

Replacing Genetic Sub-Sequences

[0070] A method by which an existing sub-sequence is removed using the flanking cleavage sites of this sub-sequence, and a new sub-sequence or collection of sub-sequences, which contains ends compatible with the cleavage sites this creates, is inserted inserted.

Assembling of Genetic Sequences:

[0071] Any process which is used to combine synthetic or natural genetic sequences in a specific manner in order to get longer genetic sequences which contain at least parts of the used synthetic or natural genetic sequences.

Analysis of Homologous Genes:

[0072] The corresponding amino acid sequences of two or more genes are aligned to each other in a way which maximizes the correspondence between identical or similar amino acid residues at all positions. These aligned sequences are termed homologous if the percentage of the sum of identical and/or similar residues exceeds a defined threshold. This threshold is commonly regarded by those skilled in the art as being exceeded when at least 15 percent of the amino acids in the aligned genes are identical, and at least 30 percent are similar.

[0118]

TABLE 1
Summary of human immunoglobulin germline sequences used for
computing the germline membership of rearranged sequences. (A) kappa
sequences, (B) lambda sequences and (C), heavy chain sequences. (1) The
germline name used in the various calculations, (2) the references number
for the corresponding sequence (see appendix for sequence related
citations), (3) the family where each sequence belongs to and (4), the
various names found in literature for germline genes with identical amino
acid sequences.

[0119]

TABLE 2
Rearranged human sequences used for the calculation of consensus
sequences. (A) kappa sequences, (B) lambda sequences and (C), heavy
chain sequences. The table summarized the name of the sequence (1),
the length of the sequence in amino acids (2), the germline family (3) as
well as the computed germline counterpart (4). The number of amino acid
exchanges between the rearranged sequence and the germline sequence is
tabulated in (5), and the percentage of different amino acids is given in
(6). Column (7) gives the references number for the corresponding
sequence (see appendix for sequence related citations).

[0120]

TABLE 3
Assignment of rearranged V sequences to their germline counterparts.
(A) kappa sequences, (B) lambda sequences and (C), heavy chain
sequences. The germline genes are tabulated according to their family
(1), and the number of rearranged genes found for every germline gene
is given in (2).

[0121]

TABLE 4
Computation of the consensus sequence of the rearranged V kappa
sequences. (A) (SEQ ID NO: 14), V kappa subgroup 1, (B) (SEQ ID
NO: 15), V kappa subgroup 2, (C) (SEQ ID NO: 16), V kappa
subgroup 3 and (D) (SEQ ID NO: 17), V kappa subgroup 4. The
number of each amino acid found at each position is tabulated together
with the statistical analysis of the data. (1) Amino acids are given with
their standard one-letter abbreviations (and B means D or N, Z means
E or Q and X means any amino acid). The statistical analysis
summarizes the number of sequences found at each position (2), the
number of occurrences of the most common amino acid (3), the amino
acid residue which is most common at this position (4), the relative
frequency of the occurrence of the most common amino acid (5) and
the number of different amino acids found at each position (6).

[0122]

TABLE 5
Computation of the consensus sequence of the rearranged V lambda
sequences. (A) (SEQ ID NO: 18), V lambda subgroup 1, (B) (SEQ ID
NO: 19), V lambda subgroup 2, and (C) (SEQ ID NO: 20), V lambda
subgroup 3. The number of each amino acid found at each position is
tabulated together with the statistical analysis of the data.
Abbreviations are the same as in Table 4.

[0123]

TABLE 6
Computation of the consensus sequence of the rearranged V heavy
chain sequences. (A) (SEQ ID NO: 21), V heavy chain subgroup 1A,
(B) (SEQ ID NO: 22), V heavy chain subgroup 1B, (C) (SEQ ID NO:
23), V heavy chain subgroup 2, (D) (SEQ ID NO: 24), V heavy chain
subgroup 3, (E) (SEQ ID NO: 25), V heavy chain subgroup 4, (F)
(SEQ ID NO: 26), V heavy chain subgroup 5, and (G) (SEQ ID NO:
27), V heavy chain subgroup 6. The number of each amino acid found
at each position is tabulated together with the statistical analysis of the
data. Abbreviations are the same as in Table 4.

[0124] The following example describes the design of a fully synthetic human combinatorial antibody library (HuCAL), based on consensus sequences of the human immunoglobulin repertoire, and the synthesis of the consensus genes. The general procedure is outlined in FIG. 1.

1.1 Sequence Database

1.1.1 Collection and Alignment of Human Immunoglobulin Sequences

[0125] In a first step, sequences of variable domains of human immunoglobulins have been collected and divided into three sub bases: V heavy chain (VH), V kappa (Vκ) and V lambda (Vλ). For each sequence, the gene sequence was then translated into the corresponding amino acid sequence. Subsequently, all amino acid sequences were aligned according to Kabat et al. (1991). In the case of Vλ sequences, the numbering system of Chuchana et al. (1990) was used. Each of the three main databases was then divided into two further sub bases: the first sub base contained all sequences derived from rearranged V genes, where more than 70 positions of the sequence were known. The second sub base contained all germline gene segments (without the D- and J-minigenes; pseudogenes with internal stop codons were also removed). In all cases, where germline sequences with identical amino acid sequence but different names were found, only one sequence was used (see Table 1). The final databases of rearranged sequences contained 386, 149 and 674 entries for Vκ, Vλ and VH, respectively. The final databases of germline sequences contained 48, 26 and 141 entries for Vκ, Vλ and VH, respectively.

1.1.2 Assignment of Sequences to Subgroups

[0126] The sequences in the three germline databases where then grouped according to sequence homology (see also Tomlinson et al., 1992, Williams & Winter, 1993, and Cox et al., 1994). In the case of Vκ, 7 families could be established. Vλ was divided into 8 families and VH into 6 families. The VH germline genes of the VH7 family (Van Dijk et al., 1993) were grouped into the VH1 family, since the genes of the two families are highly homologous. Each family contained different numbers of germline genes, varying from 1 (for example VH6) to 47 (VH3).

1.2 Analysis of Sequences

1.2.1 Computation of Germline Membership

[0127] For each of the 1209 amino acid sequences in the databases of rearranged genes, the nearest germline counterpart, i.e. the germline sequence with the smallest number of amino acid differences was then calculated. After the germline counterpart was found, the number of somatic mutations which occurred in the rearranged gene and which led to amino acid exchanges could be tabulated. In 140 cases, the germline counterpart could not be calculated exactly, because more than one germline gene was found with an identical number of amino acid exchanges. These rearranged sequences were removed from the database. In a few cases, the number of amino acid exchanges was found to be unusually large (>20 for VL and >25 for VH), indicating either heavily mutated rearranged genes or derivation from germline genes not present in the database. Since it was not possible to distinguish between these two possibilities, these sequences were also removed from the database. Finally, 12 rearranged sequences were removed from the database because they were found to have very unusual CDR lengths and composition or unusual amino acids at canonical positions (see below). In summary, 1023 rearranged sequences out of 1209 (85%) could be clearly assigned to their germline counterparts (see Table 2).

[0128] After this calculation, every rearranged gene could be arranged in one of the families established for the germline genes. Now the usage of each germline gene, i.e. the number of rearranged genes which originate from each germline gene, could be calculated (see Table 2). It was found that the usage was strongly biased towards a subset of germline genes, whereas most of the germline genes were not present as rearranged genes in the database and therefore apparently not used in the immune system (Table 3). This observation had already been reported in the case of Vκ (Cox, et al., 1994). All germline gene families, where no or only very few rearranged counterparts could be assigned, were removed from the database, leaving 4 Vκ, 3 Vλ, and 6 VH families.

1.2.2 Analysis of CDR Conformations

[0129] The conformation of the antigen binding loops of antibody molecules, the CDRs, is strongly dependent on both the length of the CDRs and the amino acid residues located at the so-called canonical positions (Chothia & Lesk, 1987). It has been found that only a few canonical structures exist, which determine the structural repertoire of the immunoglobulin variable domains (Chothia et al., 1989). The canonical amino acid positions can be found in CDR as well as framework regions. The 13 used germline families defined above (7 VL and 6 VH) were now analyzed for their canonical structures in order to define the structural repertoire encoded in these families.

[0130] In 3 of the 4 Vκ families (Vκ1, 2 and 4), one different type of CDR1 conformation could be defined for every family. The family Vκ3 showed two types of CDR1 conformation: one type which was identical to Vκ1 and one type only found in Vκ3. All Vκ CDR2s used the same type of canonical structure. The CDR3 conformation is not encoded in the germline gene segments. Therefore, the 4 Vκ families defined by sequence homology and usage corresponded also to 4 types of canonical structures found in Vκ germline genes.

[0131] The 3 Vκ families defined above showed 3 types of CDR1 conformation, each family with one unique type. The Vκ1 family contained 2 different CDR1 lengths (13 and 14 amino acids), but identical canonical residues, and it is thought that both lengths adopt the same canonical conformation (Chothia & Lesk, 1987). In the CDR2 of the used Vλ germlines, only one canonical conformation exists, and the CDR3 conformation is not encoded in the germline gene segments. Therefore, the 3 Vλ families defined by sequence homology and usage corresponded also to 3 types of canonical structures.

[0132] The structural repertoire of the human VH sequences was analyzed in detail by Chothia et al., 1992. In total, 3 conformations of CDR1 (H1-1, H1-2 and H1-3) and 6 conformations of CDR2 (H2-1, H2-2, H2-3, H2-4, H2-5 and H2-x) could be defined. Since the CDR3 is encoded in the D- and J-minigene segments, no particular canonical residues are defined for this CDR.

[0133] All the members of the VH1 family defined above contained the CDR1 conformation H1-1, but differed in their CDR2 conformation: the H2-2 conformation was found in 6 germline genes, whereas the conformation H2-3 was found in 8 germline genes. Since the two types of CDR2 conformations are defined by different types of amino acid at the framework position 72, the VH1 family was divided into two subfamilies: VH1A with CDR2 conformation H2-2 and VH1B with the conformation H2-3. The members of the VH2 family all had the conformations H1-3 and H2-1 in CDR1 and CDR2, respectively. The CDR1 conformation of the VH3 members was found in all cases to be H1-1, but 4 different types were found in CDR2 (H2-1, H2-3, H2-4 and H2-x). In these CDR2 conformations, the canonical framework residue 71 is always defined by an arginine. Therefore, it was not necessary to divide the VH3 family into subfamilies, since the 4 types of CDR2 conformations were defined solely by the CDR2 itself. The same was true for the VH4 family. Here, all 3 types of CDR1 conformations were found, but since the CDR1 conformation was defined by the CDR itself (the canonical framework residue 26 was found to be glycine in all cases), no subdivisions were necessary. The CDR2 conformation of the VH4 members was found to be H2-1 in all cases. All members of the VH5 family were found to have the conformation H1-1 and H2-2, respectively. The single germline gene of the VH6 family had the conformations H1-3 and H2-5 in CDR1 and CDR2, respectively.

[0134] In summary, all possible CDR conformations of the Vκ and Vλ genes were present in the 7 families defined by sequence comparison. From the 12 different CDR conformations found in the used VH germline genes, 7 could be covered by dividing the family VH1 into two subfamilies, thereby creating 7 VH families. The remaining 5 CDR conformations (3 in the VH3 and 2 in the VH4 family) were defined by the CDRs themselves and could be created during the construction of CDR libraries. Therefore, the structural repertoire of the used human V genes could be covered by 49 (7×7) different frameworks.

1.2.3 Computation of Consensus Sequences

[0135] The 14 databases of rearranged sequences (4 Vκ, 3 Vλ, and 7 VH) were used to compute the HuCAL consensus sequences of each subgroup (4 HuCAL-Vκ, 3 HuCAL-Vλ, 7 HuCAL-VH, see Table 4, 5 and 6). This was done by counting the number of amino acid residues used at each position (position variability) and subsequently identifying the amino acid residue most frequently used at each position. By using the rearranged sequences instead of the used germline sequences for the calculation of the consensus, the consensus was weighted according to the frequency of usage. Additionally, frequently mutated and highly conserved positions could be identified. The consensus sequences were cross-checked with the consensus of the germline families to see whether the rearranged sequences were biased at certain positions towards amino acid residues which do not occur in the collected germline sequences, but this was found not to be the case. Subsequently, the number of differences of each of the 14 consensus sequences to each of the germline sequences found in each specific family was calculated. The overall deviation from the most homologous germline sequence was found to be 2.4 amino acid residues (s.d.=2.7), ensuring that the “artificial” consensus sequences can still be considered as truly human sequences as far as immunogenicity is concerned.

1.3 Structural Analysis

[0136] So far, only sequence information was used to design the consensus sequences. Since it was possible that during the calculation certain artificial combinations of amino acid residues have been created, which are located far away in the sequence but have contacts to each other in the three dimensional structure, leading to destabilized or even misfolded frameworks, the 14 consensus sequences were analyzed according to their structural properties.

[0137] It was rationalized that all rearranged sequences present in the database correspond to functional and therefore correctly folded antibody molecules. Hence, the most homologous rearranged sequence was calculated for each consensus sequence. The positions where the consensus differed from the rearranged sequence were identified as potential “artificial residues” and inspected.

[0138] The inspection itself was done in two directions. First, the local sequence stretch around each potentially “artificial residue” was compared with the corresponding stretch of all the rearranged sequences. If this stretch was found to be truly artificial, i.e. never occurred in any of the rearranged sequences, the critical residue was converted into the second most common amino acid found at this position and analyzed again. Second, the potentially “artificial residues” were analyzed for their long range interactions. This was done by collecting all available structures of human antibody variable domains from the corresponding PDB files and calculating for every structure the number and type of interactions each amino acid residue established to each side-chain. These “interaction maps” were used to analyze the probable side-chain/side-chain interactions of the potentially “artificial residues”. As a result of this analysis, the following residues were exchanged (given is the name of the gene, the position according to Kabat's numbering scheme, the amino acid found at this position as the most abundant one and the amino acid which was used instead):

VH2: S₆₅T

Vκ1: N₃₄A,

Vλ3: G₉A, D₆₀A, R₇₇S

Vκ3: V₇₈T

1.4 Design of CDR Sequences

[0139] The process described above provided the complete consensus sequences derived solely from the databases of rearranged sequences. It was rationalized that the CDR1 and CDR2 regions should be taken from the databases of used germline sequences, since the CDRs of rearranged and mutated sequences are biased towards their particular antigens. Moreover, the germline CDR sequences are known to allow binding to a variety of antigens in the primary immune response, where only CDR3 is varied. Therefore, the consensus CDRs obtained from the calculations described above were replaced by germline CDRs in the case of VH and Vκ. In the case of Vλ, a few amino acid exchanges were introduced in some of the chosen germline CDRs in order to avoid possible protease cleavage sites as well as possible structural constraints.

[0140] The CDRs of following germline genes have been chosen:

[0141]

HuCAL gene	CDR1	CDR2
HuCAL-VH1A	VH1-12-1	VH1-12-1
HuCAL-VH1B	VH1-13-16	VH1-13-6, -7, -8, -9
HuCAL-VH2	VH2-31-10, -11, -12, -13	VH2-31-3, -4
HuCAL-VH3	VH3-13-8, -9, -10	VH3-13-8, -9, -10
HuCAL-VH4	VH4-11-7 to -14	VH4-11-8, -9, -11, -12, -14,
		-16
		VH4-31-17, -18, -19, -20
HuCAL-VH5	VH5-12-1, -2	VH5-12-1, -2
HuCAL-VH6	VH6-35-1	VH6-35-1
HuCAL-Vκ1	Vκ1-14, -15	Vκ1-2, -3, -4, -5, -7, -8, -12,
		-13, -18, -19
HuCAL-Vκ2	Vκ2-6	Vκ2-6
HuCAL-Vκ3	Vκ3-1, -4	Vκ3-4
HuCAL-Vκ4	Vκ4-1	Vκ4-1
HuCAL-Vλ1	HUMLV117, DPL5	DPL5
HuCAL-Vλ2	DPL11, DPL12	DPL12
HuCAL-Vλ3	DPL23	HUMLV318

[0142] In the case of the CDR3s, any sequence could be chosen since these CDRs were planned to be the first to be replaced by oligonucleotide libraries. In order to study the expression and folding behavior of the consensus sequences in E. coli, it would be useful to have all sequences with the same CDR3, since the influence of the CDR3s on the folding behavior would then be identical in all cases. The dummy sequences QQHYTTPP (see, for instance, positions 89–96 of SEQ ID NO: 28 and positions 88–95 of SEQ ID NO: 34) and ARWGGDGFYAMDY (positions 97–109 of SEQ ID NOS 35 & 36) were selected for the VL chains (kappa and lambda) and for the VH chains, respectively. These sequences are known to be compatible with antibody folding in E. coli (Carter et al., 1992).

1.5 Gene Design

[0143] The final outcome of the process described above was a collection of 14 HuCAL amino acid sequences, which represent the frequently used structural antibody repertoire of the human immune system (see FIG. 2). These sequences were back-translated into DNA sequences. In a first step, the back-translation was done using only codons which are known to be frequently used in E. coli. These gene sequences were then used for creating a database of all possible restriction endonuclease sites, which could be introduced without changing the corresponding amino acid sequences. Using this database, cleavage sites were selected which were located at the flanking regions of all sub-elements of the genes (CDRs and framework regions) and which could be introduced in all HuCAL VH, Vκ or Vλ genes simultaneously at the same position. In a few cases it was not possible to find cleavage sites for all genes of a subgroup. When this happened, the amino acid sequence was changed, if this was possible according to the available sequence and structural information. This exchange was then analyzed again as described above. In total, the following 6 amino acid residues were exchanged during this design (given is the name of the gene, the position according to Kabat's numbering scheme, the amino acid found at this position as the most abundant one and the amino acid which was used instead):

VH2: T₃Q

VH6: S₄₂G

Vκ3: E₁D, I₅₈V

Vκ4: K₂₄R

Vλ3: T₂₂S

[0144] In one case (5′-end of VH framework 3) it was not possible to identify a single cleavage site for all 7 VH genes. Two different type of cleavage sites were used instead: BstEII for HuCAL VH1A, VH1B, VH4 and VH5, and NspV for HuCAL VH2, VH3, VH4 and VH6.

[0145] Several restriction endonuclease sites were identified, which were not located at the flanking regions of the sub-elements but which could be introduced in every gene of a given group without changing the amino acid sequence. These cleavage sites were also introduced in order to make the system more flexible for further improvements. Finally, all but one remaining restriction endonuclease sites were removed in every gene sequence. The single cleavage site, which was not removed was different in all genes of a subgroup and could be therefore used as a “fingerprint” site to ease the identification of the different genes by restriction digest. The designed genes, together with the corresponding amino acid sequences and the group-specific restriction endonuclease sites are shown in FIGS. 3, 4 and 5, respectively.

1.6 Gene Synthesis and Cloning

[0146] The consensus genes were synthesized using the method described by Prodromou & Pearl, 1992, using the oligonucleotides shown in FIG. 6. Gene segments encoding the human constant domains Cκ, Cλ and CH1 were also synthesized, based on sequence information given by Kabat et al., 1991 (see FIG. 6 and FIG. 7). Since for both the CDR3 and the framework 4 gene segments identical sequences were chosen in all HuCAL Vκ, Vλ and VH genes, respectively, this part was constructed only once, together with the corresponding gene segments encoding the constant domains. The PCR products were cloned into pCR-Script KS(+) (Stratagene, Inc.) or pZErO-1 (Invitrogen, Inc.) and verified by sequencing.

[0147] A combination of two of the synthetic consensus genes was chosen after construction to test whether binding antibody fragments can be isolated from a library based on these two consensus frameworks. The two genes were cloned as a single-chain Fv (scFv) fragment, and a VH-CDR3 library was inserted. In order to test the library for the presence of functional antibody molecules, a selection procedure was carried out using the small hapten fluorescein bound to BSA (FITC-BSA) as antigen.

2.1 Cloning of the HuCAL VH3-Vk2 scFv Fragment

[0148] In order to test the design of the consensus genes, one randomly chosen combination of synthetic light and heavy gene (HuCAL-Vκ2 and HuCAL-VH3) was used for the construction of a single-chain antibody (scFv) fragment. Briefly, the gene segments encoding the VH3 consensus gene and the CH1 gene segment including the CDR3-framework 4 region, as well as the Vκ2 consensus gene and the Cκ gene segment including the CDR3-framework 4 region were assembled yielding the gene for the VH3-CH1 Fd fragment and the gene encoding the Vκ2-Cκ light chain, respectively. The CH1 gene segment was then replaced by an oligonucleotide (SEQ ID NOS 2 & 3, respectively) cassette encoding a 20-mer peptide linker (SEQ ID NO: 1) with the sequence AGGGSGGGGSGGGGSGGGGS. The two oligonucleotides encoding this linker were 5′-TCAGCGGGTGGCGGTTCTGGCGGCGGTGGGAGCGGTG GCGGTGGTTCTGGCGGTGGTGGTTCCGATATCGGTCCACGTACGG-3′ and 5′-AATTCCGTACGTGGACCGATATCGGAACCACCACCGCCAGA ACCACCGCCACCGCTCCCACCGCCGCCAGAACCGCCACCCGC-3′, respectively. Finally, the HuCAL-Vκ2 gene was inserted via EcoRV and BsiWI into the plasmid encoding the HuCAL-VH3-linker fusion, leading to the final gene HuCAL-VH3-Vκ2, which encoded the two consensus sequences in the single-chain format VH-linker-VL. The complete coding sequence is shown in FIG. 8.

2.2 Construction of a Monovalent Phage-Display Phagemid Vector pIG10.3

[0149] Phagemid pIG10.3 (FIG. 9) was constructed in order to create a phage-display system (Winter et al., 1994) for the H3κ2 scFv gene. Briefly, the EcoRI/HindIII restriction fragment in the phagemid vector pIG10 (Ge et al., 1995) was replaced by the c-myc followed by an amber codon (which encodes an glutamate in the amber-suppresser strain XL1 Blue and a stop codon in the non-suppresser strain JM83) and a truncated version of the gene III (fusion junction at codon 249, see Lowman et al., 1991) through PCR mutagenesis.

2.3 Construction of H-CDR3 Libraries

[0150] Heavy chain CDR3 libraries of two lengths (10 and 15 amino acids) were constructed using trinucleotide codon containing oligonucleotides (Virnekas et al., 1994) as templates and the oligonucleotides complementing the flanking regions as primers. To concentrate only on the CDR3 structures that appear most often in functional antibodies, we kept the salt-bridge of R_H94 and D_H101 in the CDR3 loop. For the 15-mer library, both phenylalanine and methionine were introduced at position 100 since these two residues were found to occur quite often in human CDR3s of this length (not shown). For the same reason, valine and tyrosine were introduced at position 102. All other randomized positions contained codons for all amino acids except cystein, which was not used in the trinucleotide mixture.

[0151] The CDR3 libraries of lengths 10 and 15 were generated from the PCR fragments using oligonucleotide templates (SEQ ID NOS 4 & 5, respectively) O3HCDR103T (5′-GATACGGCCGTGTATTATTGCGCGCGT (TRI)₆ GATTATTGGGGCCAAGGCACCCTG-3′) and O3HCDR153T (5′-GATACGGCCGTGTATTATTGCGCGCGT(TRI)₆ (TTT/ATG)GAT(GTT/TAT)TGGGGCCAAGGCACCCTG-3′), and primers (SEQ ID NOS 6 & 7, respectively) O3HCDR35 (5′-GATACGGCCGTGTATTATTGC-3′) and O3HCDR33 (5′-CAGGGTGCCTTGGCCCC-3′), where TRI are trinucleotide mixtures representing all amino acids without cystein, (TTT/ATG) and (GTT/TAT) are trinucleotide mixtures encoding the amino acids phenylalanine/methionine and valine/tyrosine, respectively. The potential diversity of these libraries was 4.7×10⁷ and 3.4×10¹⁰ for 10-mer and 15-mer library, respectively. The library cassettes were first synthesized from PCR amplification of the oligo templates in the presence of both primers: 25 pmol of the oligo template O3HCDR103T or O3HCDR153T, 50 pmol each of the primers O3HCDR35 and O3HCDR33, 20 nmol of dNTP, 10× buffer and 2.5 units of Pfu DNA polymerase (Stratagene) in a total volume of 100 ml for 30 cycles (1 minute at 92° C., 1 minute at 62° C. and 1 minute at 72° C.). A hot-start procedure was used. The resulting mixtures were phenol-extracted, ethanol-precipitated and digested overnight with EagI and Styl. The vector pIG10.3-sCH3κ2cat, where the EagI-Styl fragment in the vector pIG10.3-sCH3κ2 encoding the H-CDR3 was replaced by the chloramphenicol acetyltransferase gene (cat) flanked with these two sites, was similarly digested. The digested vector (35 μg) was gel-purified and ligated with 100 μg of the library cassette overnight at 16° C. The ligation mixtures were isopropanol precipitated, air-dried and the pellets were redissolved in 100 ml of ddH2O. The ligation was mixed with 1 ml of freshly prepared electrocompetent XL 1 Blue on ice. 20 rounds of electroporation were performed and the transformants were diluted in SOC medium, shaken at 37° C. for 30 minutes and plated out on large LB plates (Amp/Tet/Glucose) at 37° C. for 6–9 hrs. The number of transformants (library size) was 3.2×10⁷ and 2.3×10⁷ for the 10-mer and the 15-mer library, respectively. The colonies were suspended in 2xYT medium (Amp/Tet/Glucose) and stored as glycerol culture. In order to test the quality of the initial library, phagemids from 24 independent colonies (12 from the 10-mer and 12 from the 15-mer library, respectively) were isolated and analyzed by restriction digestion and sequencing. The restriction analysis of the 24 phagemids indicated the presence of intact vector in all cases. Sequence analysis of these clones (see FIG. 10) indicated that 22 out of 24 contained a functional sequence in their heavy chain CDR3 regions. 1 out of 12 clones of the 10-mer library had a CDR3 of length 9 instead of 10, and 2 out of 12 clones of the 15-mer library had no open reading frame, thereby leading to a non-functional scFv; one of these two clones contained two consecutive inserts, but out of frame (data not shown). All codons introduced were presented in an even distribution.

[0152] Expression levels of individual library members were also measured. Briefly, 9 clones from each library were grown in 2xYT medium containing Amp/Tet/0.5% glucose at 37° C. overnight. Next day, the cultures were diluted into fresh medium with Amp/Tet. At an OD_600nm of 0.4, the cultures were induced with 1 mM of IPTG and shaken at RT overnight. Then the cell pellets were suspended in 1 ml of PBS buffer+1 mM of EDTA. The suspensions were sonicated and the supernatants were separated on an SDS-PAGE under reducing conditions, blotted on nylon membrane and detected with anti-FLAG M1 antibody (see FIG. 11). From the nine clones of the 10-mer library, all express the scFv fragments. Moreover, the gene III scFv fusion proteins were present in all cases. Among the nine clones from the 15-mer library analyzed, 6/9 (67%) led to the expression of both scFv and the gene III/scFv fusion proteins. More importantly, all clones expressing the scFvs and gene III/scFv fusions gave rise to about the same level of expression.

2.4 Biopanning

[0153] Phages displaying the antibody libraries were prepared using standard protocols. Phages derived from the 10-mer library were mixed with phages from the 15-mer library in a ratio of 20:1 (1×10¹⁰ cfu/well of the 10-mer and 5×10⁸ cfu/well of the 15-mer phages, respectively). Subsequently, the phage solution was used for panning in ELISA plates (Maxisorp, Nunc) coated with FITC-BSA (Sigma) at concentration of 100 μg/ml in PBS at 4° C. overnight. The antigen-coated wells were blocked with 3% powder milk in PBS and the phage solutions in 1% powder milk were added to each well and the plate was shaken at RT for 1 hr. The wells were then washed with PBST and PBS (4 times each with shaking at RT for 5 minutes). The bound phages were eluted with 0.1 M triethylamine (TEA) at RT for 10 minutes. The eluted phage solutions were immediately neutralized with ½ the volume of 1 M Tris.Cl, pH 7.6. Eluted phage solutions (ca. 450 μl) were used to infect 5 ml of XL1 Blue cells at 37° C. for 30 min. The infected cultures were then plated out on large LB plates (Amp/Tet/Glucose) and allowed to grow at 37° C. until the colonies were visible. The colonies were suspended in 2xYT medium and the glycerol cultures were made as above described. This panning round was repeated twice, and in the third round elution was carried out with addition of fluorescein in a concentration of 100 μg/ml in PBS. The enrichment of specific phage antibodies was monitored by panning the initial as well as the subsequent fluorescein-specific sub-libraries against the blocking buffer (FIG. 12). Antibodies with specificity against fluorescein were isolated after 3 rounds of panning.

2.5 ELISA Measurements

[0154] One of the criteria for the successful biopanning is the isolation of individual phage clones that bind to the targeted antigen or hapten. We undertook the isolation of anti-FITC phage antibody clones and characterized them first in a phage ELISA format. After the 3rd round of biopanning (see above), 24 phagemid containing clones were used to inoculate 100 μl of 2xYT medium (Amp/Tet/Glucose) in an ELISA plate (Nunc), which was subsequently shaken at 37° C. for 5 hrs. 100 μl of 2xYT medium (Amp/Tet/1 mM IPTG) were added and shaking was continued for 30 minutes. A further 100 μl of 2xYT medium (Amp/Tet) containing the helper phage (1×10⁹ cfu/well) was added and shaking was done at RT for 3 hrs. After addition of kanamycin to select for successful helper phage infection, the shaking was continued overnight. The plates were then centrifuged and the supernatants were pipetted directly into ELISA wells coated with 100 μl FITC-BSA (100 μg/ml) and blocked with milk powder. Washing was performed similarly as during the panning procedure and the bound phages were detected with anti-M13 antibody-POD conjugate (Pharmacia) using soluble POD substrate (Boehringer-Mannheim). Of the 24 clones screened against FITC-BSA, 22 were active in the ELISA (FIG. 13). The initial libraries of similar titer gave rise to no detectable signal.

[0155] Specificity for fluorescein was measured in a competitive ELISA. Periplasmic fractions of five FITC specific scFvs were prepared as described above. Western blotting indicated that all clones expressed about the same amount of scFv fragment (data not shown). ELISA was performed as described above, but additionally, the periplasmic fractions were incubated 30 min at RT either with buffer (no inhibition), with 10 mg/ml BSA (inhibition with BSA) or with 10 mg/ml fluorescein (inhibition with fluorescein) before adding to the well. Binding scFv fragment was detected using the anti-FLAG antibody M1. The ELISA signal could only be inhibited, when soluble fluorescein was added, indicating binding of the scFvs was specific for fluorescein (FIG. 14).

2.6 Sequence Analysis

[0156] The heavy chain CDR3 region of 20 clones were sequenced in order to estimate the sequence diversity of fluorescein binding antibodies in the library (FIG. 15). In total, 16 of 20 sequences (80%) were different, showing that the constructed library contained a highly diverse repertoire of fluorescein binders. The CDR3s showed no particular sequence homology, but contained on average 4 arginine residues. This bias towards arginine in fluorescein binding antibodies had already been described by Barbas et al., 1992.

2.7 Production

[0157] E. coli JM83 was transformed with phagemid DNA of 3 selected clones and cultured in 0.5 L 2xYT medium. Induction was carried out with 1 mM IPTG at OD_600nm=0.4 and growth was continued with vigorous shaking at RT overnight. The cells were harvested and pellets were suspended in PBS buffer and sonicated. The supernatants were separated from the cell debris via centrifugation and purified via the BioLogic system (Bio-Rad) by with a POROS®MC 20 column (IMAC, PerSeptive Biosystems, Inc.) coupled with an ion-exchange chromatography column. The ion-exchange column was one of the POROS®HS, CM or HQ or PI 20 (PerSeptive Biosystems, Inc.) depended on the theoretical pI of the scFv being purified. The pH of all the buffers was adjusted to one unit lower or higher than the pI of the scFv being purified throughout. The sample was loaded onto the first IMAC column, washed with 7 column volumes of 20 mM sodium phosphate, 1 M NaCl and 10 mM imidazole. This washing was followed by 7 column volumes of 20 mM sodium phosphate and 10 mM imidazole. Then 3 column volumes of an imidazole gradient (10 to 250 mM) were applied and the eluent was connected directly to the ion-exchanger. Nine column volumes of isocratic washing with 250 mM imidazole was followed by 15 column volumes of 250 mM to 100 mM and 7 column volumes of an imidazole/NaCl gradient (100 to 10 mM imidazole, 0 to 1 M NaCl). The flow rate was 5 ml/min. The purity of scFv fragments was checked by SDS-PAGE Coomassie staining (FIG. 16). The concentration of the fragments was determined from the absorbance at 280 nm using the theoretically determined extinction coefficient (Gill & von Hippel, 1989). The scFv fragments could be purified to homogeneity (see FIG. 16). The yield of purified fragments ranged from 5 to 10 mg/L/OD.

[0158] In order to test the library used in Example 2 further, a new selection procedure was carried out using a variety of antigens comprising β-estradiol, testosterone, Lewis-Y epitope (LeY), interleukin-2 (IL-2), lymphotoxin-β(LT-β), E-selectin ligand-1 (ESL-1), and BSA.

3.1 Biopanning

[0159] The library and all procedures were identical to those described in Example 2. The ELISA plates were coated with β-estradiol-BSA (100 μg/ml), testosterone-BSA (100 μg/ml), LeY-BSA (20 μg/ml) IL-2 (20 μg/ml), ESL-1 (20 μg/ml) and BSA (100 μg/ml), LT-β (denatured protein, 20 μg/ml). In the first two rounds, bound phages were eluted with 0.1 M triethylamine (TEA) at RT for 10 minutes. In the case of BSA, elution after three rounds of panning was carried out with addition of BSA in a concentration of 100 μg/ml in PBS. In the case of the other antigens, third round elution was done with 0.1 M triethylamine. In all cases except LeY, enrichment of binding phages could be seen (FIG. 17). Moreover, a repetition of the biopanning experiment using only the 15-mer library resulted in the enrichment of LeY-binding phages as well (data not shown).

3.2. ELISA Measurements

[0160] Clones binding to β-estradiol, testosterone, LeY, LT-β, ESL-1 and BSA were further analyzed and characterized as described in Example 2 for FITC. ELISA data for anti-β-estradiol and anti-ESL-1 antibodies are shown in FIG. 18. In one experiment, selectivity and cross-reactivity of binding scFv fragments were tested. For this purpose, an ELISA plate was coated with FITC, testosterone, β-estradiol, BSA, and ESL-1, with 5 wells for each antigen arranged in 5 rows, and 5 antibodies, one against each of the antigens, were screened against each of the antigens. FIG. 19 shows the specific binding of the antibodies to the antigen it was selected for, and the low cross-reactivity with the other four antigens.

3.3 Sequence Analysis

[0161] The sequencing data of several clones against β-estradiol (34 clones), testosterone (12 clones), LT-β (23 clones), ESL-1 (34 clones), and BSA (10 clones) are given in FIGS. 20 to 24.

[0162] To be able to take advantage of the modularity of the consensus gene repertoire, a vector system had to be constructed which could be used in phage display screening of HuCAL libraries and subsequent optimization procedures. Therefore, all necessary vector elements such as origins of single-stranded or double-stranded replication, promotor/operator, repressor or terminator elements, resistance genes, potential recombination sites, gene III for display on filamentous phages, signal sequences, or detection tags had to be made compatible with the restriction site pattern of the modular consensus genes. FIG. 25 shows a schematic representation of the pCAL vector system and the arrangement of vector modules and restriction sites therein. FIG. 25a shows a list of all restriction sites which are already incorporated into the consensus genes or the vector elements as part of the modular system or which are not yet present in the whole system. The latter could be used in a later stage for the introduction of or within new modules.

4.1 Vector Modules

[0163] A series of vector modules was constructed where the restriction sites flanking the gene sub-elements of the HuCAL genes were removed, the vector modules themselves being flanked by unique restriction sites. These modules were constructed either by gene synthesis or by mutagenesis of templates. Mutagenesis was done by add-on PCR, by site-directed mutagenesis (Kunkel et al., 1991) or multisite oligonucleotide-mediated mutagenesis (Sutherland et al., 1995; Perlak, 1990) using a PCR-based assembly method.

[0164] FIG. 26 contains a list of the modules constructed. Instead of the terminator module M9 (HindIII-Ipp-PacI), a larger cassette M9II was prepared to introduce FseI as additional restriction site. M9II can be cloned via HindIII/BsrGI.

[0165] All vector modules were characterized by restriction analysis and sequencing. In the case of module M11-II, sequencing of the module revealed a two-base difference in positions 164/65 compared to the sequence database of the template. These two different bases (CA→GC) created an additional BanII site. Since the same two-base difference occurs in the f1 origin of other bacteriophages, it can be assumed that the two-base difference was present in the template and not created by mutagenesis during cloning. This BanII site was removed by site-directed mutagenesis, leading to module M11-III. The BssSI site of module M14 could initially not be removed without impact on the function of the ColE1 origin, therefore M14-Ext2 was used for cloning of the first pCAL vector series. FIGS. 29 to 34 are showing the functional maps and sequences of the modules used for assembly of the modular vector pCAL4 (see below). The functional maps and sequences of additional modules can be found in FIGS. 35A-9 to 35A-75. FIGS. 35A-76 to 35A-80 contain lists of oligonucleotides and primers used for the synthesis of the modules.

4.2 Cloning Vector pMCS

[0166] To be able to assemble the individual vector modules, a cloning vector pMCS containing a specific multi-cloning site (MCS) was constructed. First, an MCS cassette (FIG. 27) was made by gene synthesis. This cassette contains all those restriction sites in the order necessary for the sequential introduction of all vector modules and can be cloned via the 5′-HindIII site and a four base overhang at the 3′-end compatible with an AatII site. The vector pMCS (FIG. 28) was constructed by digesting pUC19 with AatII and HindIII, isolating the 2174 base pair fragment containing the bla gene and the ColE1 origin, and ligating the MCS cassette.

4.3 Cloning of Modular Vector pCAL4

[0167] This was cloned step by step by restriction digest of pMCS and subsequent ligation of the modules M1 (via AatII/XbaI), M7III (via EcoRI/HindIII), and M9II (via HindIII/BsrGI), and M11-II (via BsrGI/NheI). Finally, the bla gene was replaced by the cat gene module M17 (via AatII/BgIII), and the wild type ColE1 origin by module M14-Ext2 (via BgIII/NheI). FIG. 35 is showing the functional map and the sequence of pCAL4.

4.4 Cloning of Low-Copy Number Plasmid Vectors pCALO

[0168] A series of low-copy number plasmid vectors was constructed in a similar way using the p15A module M12 instead of the ColE1 module M14-Ext2. FIGS. 35A-9 to 35A-75 show the functional maps and sequences of the vectors pCALO1 to pCALO3.

5.1. Cloning of All 49 HuCAL scFv Fragments

[0169] All 49 combinations of the 7 HuCAL-VH and 7 HuCAL-VL consensus genes were assembled as described for the HuCAL VH3-Vκ2 scFv in Example 2 and inserted into the vector pBS12, a modified version of the pLisc series of antibody expression vectors (Skerra et al., 1991).

5.2 Construction of a CDR Cloning Cassette

[0170] For replacement of CDRs, a universal β-lactamase cloning cassette was constructed having a multi-cloning site at the 5′-end as well as at the 3′-end. The 5′-multi-cloning site comprises all restriction sites adjacent to the 5′-end of the HuCAL VH and VL CDRs, the 3′-multi-cloning site comprises all restriction sites adjacent to the 3′ end of the HuCAL VH and VL CDRs. Both 5′- and 3′-multi-cloning site were prepared as cassettes via add-on PCR using synthetic oligonucleotides as 5′- and 3′-primers using wild type β-lactamase gene as template. FIG. 36 shows the functional map and the sequence of the cassette bla-MCS.

5.3. Preparation of VL-CDR3 Library Cassettes

[0171] The VL-CDR3 libraries comprising 7 random positions were generated from the PCR fragments using oligonucleotide templates Vκ1&Vκ3, Vκ2 and Vκ4 and primers O_K3L_—5 and O_K3L_—3 (FIG. 37) for the Vκ genes, and Vλ and primers (SEQ ID NO: 8) O_L3L_—5 (5′-GCAGAAGGCGAACGTCC-3′) and O_L3LA_—3 (FIG. 38) for the Vλ genes. Construction of the cassettes was performed as described in Example 2.3.

5.4 Cloning of HuCAL scFv Genes with VL-CDR3 Libraries

[0172] Each of the 49 single-chains was subcloned into pCAL4 via XbaI/EcoRI and the VL-CDR3 replaced by the β-lactamase cloning cassette via BbsI/MscI, which was then replaced by the corresponding VL-CDR3 library cassette synthesized as described above. This CDR replacement is described in detail in Example 2.3 where the cat gene was used.

5.5 Preparation of VH-CDR3 Library Cassette

[0173] The VH-CDR3 libraries were designed and synthesized as described in Example 2.3.

5.6 Cloning of HuCAL scFv Genes with VL- and VH-CDR3 Libraries

[0174] Each of the 49 single-chain VL-CDR3 libraries was digested with BssHII/StyI to replace VH-CDR3. The “dummy” cassette digested with BssHII/Styl was inserted, and was then replaced by a corresponding VH-CDR3 library cassette synthesized as described above.

[0175] Expression and toxicity studies were performed using the scFv format VH-linker-VL. All 49 combinations of the 7 HuCAL-VH and 7 HuCAL-VL consensus genes assembled as described in Example 5 were inserted into the vector pBS13, a modified version of the pLisc series of antibody expression vectors (Skerra et al., 1991). A map of this vector is shown in FIG. 39.

[0176] E. coli JM83 was transformed 49 times with each of the vectors and stored as glycerol stock. Between 4 and 6 clones were tested simultaneously, always including the clone H3κ2, which was used as internal control throughout. As additional control, the McPC603 scFv fragment (Knappik & Plückthun, 1995) in pBS13 was expressed under identical conditions. Two days before the expression test was performed, the clones were cultivated on LB plates containing 30 μg/ml chloramphenicol and 60 mM glucose. Using this plates an 3 ml culture (LB medium containing 90 μg chloramphenicol and 60 mM glucose) was inoculated overnight at 37° C. Next day the overnight culture was used to inoculate 30 ml LB medium containing chloramphenicol (30 μg/ml). The starting OD_600nm was adjusted to 0.2 and a growth temperature of 30.degree. C. was used. The physiology of the cells was monitored by measuring every 30 minutes for 8 to 9 hours the optical density at 600 nm. After the culture reached an OD_600nm of 0.5, antibody expression was induced by adding IPTG to a final concentration of 1 mM. A 5 ml aliquot of the culture was removed after 2 h of induction in order to analyze the antibody expression. The cells were lysed and the soluble and insoluble fractions of the crude extract were separated as described in Knappik & Pluckthun, 1995. The fractions were assayed by reducing SDS-PAGE with the samples normalized to identical optical densities. After blotting and immunostaining using the α-FLAG antibody M1 as the first antibody (see Ge et al., 1994) and an Fc-specific anti-mouse antiserum conjugated to alkaline phosphatase as the second antibody, the lanes were scanned and the intensities of the bands of the expected size (appr. 30 kDa) were quantified densitometrically and tabulated relative to the control antibody (see FIG. 40).

7.1. Construction of L-CDR3 and H-CDR2 Library Cassettes

[0177] A L-CDR3 library cassette was prepared from the oligonucleotide (SEQ ID NO: 9) template CDR3L (5′-TGGAAGCTGAAGACGTGGGCGTGTATTATT GCCAGCAG(TR5)(TRI)₄CCG(TRI)TTTGGCCAGGGTACGAAAGTT-3′) and primer (SEQ ID NO: 10) 5′-AATTTCGTACCCTGGCC-3′ for synthesis of the complementary strand, where (TRI) was a trinucleotide mixture representing all amino acids except Cys, (TR5) comprised a trinucleotide mixture representing the 5 codons for Ala, Arg, His, Ser, and Tyr.

[0178] A H-CDR2 library cassette was prepared from the oligonucleotide template CDRsH (SEQ ID NOS 11 & 12, respectively) (5′-AGGGTCTCG AGTGGGTGAGC(TRI)ATT(TRI)_2-3(6)₂(TRI)ACC(TRI)TATGCG GATAGCGTGAAAGGCCGTTTTACCATTTCACGTGATAATTCGAAAAA CACCA-3′), and primer (SEQ ID NO: 13) 5′-TGGTGTTTTTCGAATTATCA-3′ for synthesis of the complementary strand, where (TRI) was a trinucleotide mixture representing all amino acids except Cys, (6) comprised the incorporation of (A/G) (A/C/G) T, resulting in the formation of 6 codons for Ala, Asn, Asp, Gly, Ser, and Thr, and the length distribution being obtained by performing one substoichiometric coupling of the (TRI) mixture during synthesis, omitting the capping step normally used in DNA synthesis.

[0179] DNA synthesis was performed on a 40 nmole scale, oligos were dissovled in TE buffer, purified via gel filtration using spin columns (S-200), and the DNA concentration determined by OD measurement at 260 nm (OD 1.0=40 μg/ml). 10 nmole of the oligonucleotide templates and 12 nmole of the corresponding primers were mixed and annealed at 80° C. for 1 min, and slowly cooled down to 37° C. within 20 to 30 min. The fill-in reaction was performed for 2 h at 37° C. using Klenow polymerase (2.0 μl) and 250 nmole of each dNTP. The excess of dNTPs was removed by gel filtration using Nick-Spin columns (Pharmacia), and the double-stranded DNA digested with BbsI/MscI (L-CDR3), or XhoI/SfuI (H-CDR2) over night at 37° C. The cassettes were purified via Nick-Spin columns (Pharmacia), the concentration determined by OD measurement, and the cassettes aliquoted (15 pmole) for being stored at −80° C.

7.2 Library Cloning:

[0180] DNA was prepared from the collection of FITC binding clones obtained in Example 2 (approx. 10⁴ to clones). The collection of scFv fragments was isolated via XbaI/EcoRI digest. The vector pCAL4 (100 fmole, 10 μg) described in Example 4.3 was similarly digested with XbaI/EcoRI, gel-purified and ligated with 300 fmole of the scFv fragment collection over night at 16° C. The ligation mixture was isopropanol precipitated, air-dried, and the pellets were redissolved in 100 μl of dd H₂O. The ligation mixture was mixed with 1 ml of freshly prepared electrocompetent SCS 101 cells (for optimization of L-CDR3), or XL1 Blue cells (for optimization of H-CDR2) on ice. One round of electroporation was performed and the transformants were eluted in SOC medium, shaken at 37° C. for 30 minutes, and an aliquot plated out on LB plates (Amp/Tet/Glucose) at 37° C. for 6–9 hrs. The number of transformants was 5×10⁴.

[0181] Vector DNA (100 μg) was isolated and digested (sequence and restriction map of sCH3κ2 see FIG. 8) with BbsI/MscI for optimization of L-CDR3, or XhoI/NspV for optimization of H-CDR2. 10 μg of purified vector fragments (5 pmole) were ligated with 15 pmole of the L-CDR3 or H-CDR2 library cassettes over night at 16° C. The ligation mixtures were isopropanol precipitated, air-dried, and the pellets were redissolved in 100 μl of dd H₂O. The ligation mixtures were mixed with 1 ml of freshly prepared electrocompetent XL1 Blue cells on ice. Electroporation was performed and the transformants were eluted in SOC medium and shaken at 37° C. for 30 minutes. An aliquot was plated out on LB plates (Amp/Tet/Glucose) at 37° C. for 6–9 hrs. The number of transformants (library size) was greater than 10⁸ for both libraries. The libraries were stored as glycerol cultures.

7.3. Biopanning

[0182] This was performed as described for the initial H3κ2H-CDR3 library in Example 2.1. Optimized scFvs binding to FITC could be characterized and analyzed as described in Example 2.2 and 2.3, and further rounds of optimization could be made if necessary.

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[0219]

TABLE 1A
Human kappa germline gene segments
Used	Ref-
Name1	erence2	Family3	Germline genes4
Vk1-1	9	1	O8; O18; DPK1
Vk1-2	1	1	L14; DPK2
Vk1-3	2	1	L15(1); HK101; HK146; HK189
Vk1-4	9	1	L11
Vk1-5	2	1	A30
Vk1-6	1	1	LFVK5
Vk1-7	1	1	LFVK431
Vk1-8	1	1	L1; HK137
Vk1-9	1	1	A20; DPK4
Vk1-10	1	1	L18; Va″
Vk1-11	1	1	L4; L18; Va′; V4a
Vk1-12	2	1	L5; L19(1); Vb; Vb4; DPK5; L19(2); Vb″;
			DPK6
Vk1-13	2	1	L15(2); HK134; HK166; DPK7
Vk1-14	8	1	L8; Vd; DPK8
Vk1-15	8	1	L9; Ve
Vk1-16	1	1	L12(1); HK102; V1
Vk1-17	2	1	L12(2)
Vk1-18	1	1	O12a(V3b)
Vk1-19	6	1	O2; O12; DPK9
Vk1-20	2	1	L24; Ve″; V13; DPK10
Vk1-21	1	1	O4; O14
Vk1-22	2	1	L22
Vk1-23	2	1	L23
Vk2-1	1	2	A2; DPK12
Vk2-2	6	2	O1; O11(1); DPK13
Vk2-3	6	2	O12(2); V3a
Vk2-4	2	2	L13
Vk2-5	1	2	DPK14
Vk2-6	4	2	A3; A19; DPK15
Vk2-7	4	2	A29; DPK27
Vk2-8	4	2	A13
Vk2-9	1	2	A23
Vk2-10	4	2	A7; DPK17
Vk2-11	4	2	A17; DPK18
Vk2-12	4	2	A1; DPK19
Vk3-1	11	3	A11; humkv305; DPK20
Vk3-2	1	3	L20; Vg″
Vk3-3	2	3	L2; L16; humkv328; humkv328h2;
			humkv328h5; DPK21
Vk3-4	11	3	A27; humkv325; VkRF; DPK22
Vk3-5	2	3	L25; DPK23
Vk3-6	2	3	L10(1)
Vk3-7	7	3	L10(2)
Vk3-8	7	3	L6; Vg
Vk4-1	3	4	B3; VkIV; DPK24
Vk5-1	10	5	B2; EV15
Vk6-1	12	6	A14; DPK25
Vk6-2	12	6	A10; A26; DPK26
Vk7-1	5	7	B1

[0220]

TABLE 1B
Human lambda germline gene segments
Used Name1	Reference2	Family3	Germilne genes4
DPL1	1	1
DPL2	1	1	HUMLV1L1
DPL3	1	1	HUMLV122
DPL4	1	1	VLAMBDA 1.1
HUMLV117	2	1
DPL5	1	1	HUMLV117D
DPL6	1	1
DPL7	1	1	IGLVIS2
DPL8	1	1	HUMLV1042
DPL9	1	1	HUMLV101
DPL10	1	2
VLAMBDA 2.1	3	2
DPL11	1	2
DPL12	1	2
DPL13	1	2
DPL14	1	2
DPL16	1	3	Humlv418; IGLV3S1
DPL23	1	3	VI III.1
Humlv318	4	3
DPL18	1	7	4A; HUMIGLVA
DPL19	1
DPL21	1	8	VL8.1
HUMLV801	5	8
DPL22	1	9
DPL24	1	unassigned	VLAMBDA N.2
gVLX-4.4	6	10

[0221]

TABLE 1C
Human heavy chain germline gene segments
	Ref-
Used Name1	erence2	Family3	Germline genes4
VH1-12-1	19	1	DP10; DA-2; DA-6
VH1-12-8	22	1	RR.VH1.2
VH1-12-2	6	1	hv1263
VH1-12-9	7	1	YAC-7; RR.VH1.1; 1-69
VH1-12-3	19	1	DP3
VH1-12-4	19	1	DP21; 4d275a; VH7a
VH1-12-5	18	1	1-4.1b; V1-4.1b
VH1-12-6	21	1	1D37; VH7b; 7-81; YAC-10
VH1-12-7	19	1	DP14; VH1GRR; V1-18
VH1-13-1	10	1	71-5; DP2
VH1-13-2	10	1	E3-10
VH1-13-3	19	1	DP1
VH1-13-4	12	1	V35
VH1-13-5	8	1	V1-2b
VH1-13-6	18	1	1-2; DP75
VH1-13-7	21	1	V1-2
VH1-13-8	19	1	DP8
VH1-13-9	3	1	1-1
VH1-13-10	19	1	DP12
VH1-13-11	15	1	V13C
VH1-13-12	18	1	1-3b; DP25; V1-3b
VH1-13-13	3	1	1-92
VH1-13-14	18	1	1-3; V1-3
VH1-13-15	19	1	DP15; V1-8
VH1-13-16	3	1	21-2; 3-1; DP7; V1-46
VH1-13-17	16	1	HG3
VH1-13-18	19	1	DP4; 7-2; V1-45
VH1-13-19	27	1	COS 5
VH1-1X-1	19	1	DP5; 1-24P
VH2-21-1	18	2	II-5b
VH2-31-1	2	2	VH2S12-1
VH2-31-2	2	2	VH2S12-7
VH2-31-3	2	2	VH2S12-9; DP27
VH2-31-4	2	2	VH2S12-10
VH2-31-5	14	2	V2-26; DP26; 2-26
VH2-31-6	15	2	VF2-26
VH2-31-7	19	2	DP28; DA-7
VH2-31-14	7	2	YAC-3; 2-70
VH2-31-8	2	2	VH2S12-5
VH2-31-9	2	2	VH2S12-12
VH2-31-10	18	2	II-5; V2-5
VH2-31-11	2	2	VH2S12-2; VH2S12-8
VH2-31-12	2	2	VH2S12-4; VH2S12-6
VH2-31-13	2	2	VH2S12-14
VH3-11-1	13	3	v65-2; DP44
VH3-11-2	19	3	DP45
VH3-11-3	3	3	13-2; DP48
VH3-11-4	19	3	DP52
VH3-11-5	14	3	v3-13
VH3-11-6	19	3	DP42
VH3-11-7	3	3	8-1B; YAC-5; 3-66
VH3-11-8	14	3	V3-53
VH3-13-1	3	3	22-28; DP35; V3-11
VH3-13-5	19	3	DP59; VH19; V3-35
VH3-13-6	25	3	f1-p1; DP61
VH3-13-7	19	3	DP46; GL-SJ2; COS 8; hv3005;
			hv3005f3; 3d21b; 56p1
VH3-13-8	24	3	VH26
VH3-13-9	5	3	vh26c
VH3-13-10	19	3	DP47; VH26; 3-23
VH3-13-11	3	3	1-91
VH3-13-12	19	3	DP58
VH3-13-13	3	3	1-9III; DP49; 3-30; 3d28.1
VH3-13-14	24	3	3019B9; DP50, 3-33; 3d277
VH3-13-15	27	3	COS 3
VH3-13-16	19	3	DP51
VH3-13-17	16	3	H11
VH3-13-18	19	3	DP53; COS 6; 3-74; DA-8
VH3-13-19	19	3	DP54; VH3-11; V3-7
VH3-13-20	14	3	V3-64; YAC-6
VH3-13-21	14	3	V3-48
VH3-13-22	14	3	V3-43; DP33
VH3-13-23	14	3	V3-33
VH3-13-24	14	3	V3-21; DP77
VH3-13-25	14	3	V3-20; DP32
VH3-13-26	14	3	V3-9; DP31
VH3-14-1	3	3	12-2; DP29; 3-72; DA-3
VH3-14-4	7	3	YAC-9; 3-73; MTGL
VH3-14-2	4	3	VHD26
VH3-14-3	19	3	DP30
VH3-1X-1	1	3	LSG8.1; LSG9.1; LSG10.1;
			HUM12IGVH; HUM13IGVH
VH3-1X-2	1	3	LSG11.1; HUM4IGVH
VH3-1X-3	3	3	9-1; DP38; LSG7.1; RCG1.1; LSG1.1;
			LSG3.1; LSG5.1; HUM15IGVH;
			HUM2IGVH; HUM9IGVH
VH3-1X-4	1	3	LSG4.1
VH3-1X-5	1	3	LSG2.1
VH3-1X-6	1	3	LSG6.1; HUM10IGVH
VH3-1X-7	18	3	3-15; V3-15
VH3-1X-8	1	3	LSG12.1; HUM5IGVH
VH3-1X-9	14	3	V3-49
VH4-11-1	22	4	Tou-VH4.21
VH4-11-2	17	4	VH4.21; DPG3; VH5; 4d76; V4-34
VH4-11-3	23	4	4.44
VH4-11-4	23	4	4.44.3
VH4-11-5	23	4	4.36
VH4-11-6	23	4	4.37
VH4-11-7	18	4	IV-4; 4.35; V4-4
VH4-11-8	17	4	VH4.11; 3d197d; DP71; 58p2
VH4-11-9	20	4	H7
VH4-11-10	20	4	H8
VH4-11-11	20	4	H9
VH4-11-12	17	4	VH4.16
VH4-11-13	23	4	4.38
VH4-11-14	17	4	VH4.15
VH4-11-15	11	4	58
VH4-11-16	10	4	71-4; V4-59
VH4-21-1	11	4	11
VH4-21-2	17	4	VH4.17; VH4.23; 4d255; 4.40; DP69
VH4-21-3	17	4	VH4.19; 79; V4-4b
VH4-21-4	19	4	DP70; 4d68; 4.41
VH4-21-5	19	4	DP67; VH4-4B
VH4-21-6	17	4	VH4.22; VHSP; VH-JA
VH4-21-7	17	4	VH4.13; 1-9II; 12G-1; 3d28d; 4.42;
			DP68; 4-28
VH4-21-8	26	4	hv4005; 3d24d
VH4-21-9	17	4	VH4.14
VH4-31-1	23	4	4.34; 3d230d; DP78
VH4-31-2	23	4	4.34.2
VH4-31-3	19	4	DP64; 3d216d
VH4-31-4	19	4	DP65; 4-31; 3d277d
VH4-31-5	23	4	4.33; 3d75d
VH4-31-6	20	4	H10
VH4-31-7	20	4	H11
VH4-31-8	23	4	4.31
VH4-31-9	23	4	4.32
VH4-31-10	20	4	3d277d
VH4-31-11	20	4	3d216d
VH4-31-12	20	4	3d279d
VH4-31-13	17	4	VH4.18; 4d154; DP79
VH4-31-14	8	4	V4-39
VH4-31-15	11	4	2-1; DP79
VH4-31-16	23	4	4.30
VH4-31-17	17	4	VH4.12
VH4-31-18	10	4	71-2; DP66
VH4-31-19	23	4	4.39
VH4-31-20	8	4	V4-61
VH5-12-1	9	5	VH251; DP73; VHVCW; 51-R1;
			VHVLB; VHVCH; VHVTT;
			VHVAU; VHVBLK; VhAU; V5-51
VH5-12-2	17	5	VHVJB
VH5-12-3	3	5	1-v; DP80; 5-78
VH5-12-4	9	5	VH32; VHVRG; VHVMW; 5-2R1
VH6-35- 1	4	6	VHVI; VH6; VHVIIS; VHVITE;
			VHVUB; VHVICH; VHVICW;
			VHVIBLK; VHVIMW; DP74; 6-1G1;
			V6-1

[0222]

TABLE 2A
rearranged human kappa sequences
		Computed	Germline	Diff. to	% diff. to
Name1	aa2	family3	gene4	germline5	germline6	Reference7
III-3R	108	1	O8	1	1.1%	70
No.86	109	1	O8	3	3.2%	80
AU	108	1	O8	6	6.3%	103
ROY	108	1	O8	6	6.3%	43
IC4	108	1	O8	6	6.3%	70
HIV-B26	106	1	O8	3	3.2%	8
GRI	108	1	O8	8	8.4%	30
AG	106	1	O8	8	8.6%	116
REI	108	1	O8	9	9.5%	86
CLL PATIENT 16	88	1	O8	2	2.3%	122
CLL PATIENT 14	87	1	O8	2	2.3%	122
CLL PATIENT 15	88	1	O8	2	2.3%	122
GM4672	108	1	O8	11	11.6%	24
HUM.YFC51.1	108	1	O8	12	12.6%	110
LAY	108	1	O8	12	12.6%	48
HIV-b13	106	1	O8	9	9.7%	8
MAL-NaCl	108	1	O8	13	13.7%	102
STRAb SA-1A	108	1	O2	0	0.0%	120
HuVHCAMP	108	1	O8	13	13.7%	100
CRO	108	1	O2	10	10.5%	30
Am107	108	1	O2	12	12.6%	108
WALKER	107	1	O2	4	4.2%	57
III-2R	109	1	A20	0	0.0%	70
FOG1-A4	107	1	A20	4	4.2%	41
HK137	95	1	L1	0	0.0%	10
CEA4-8A	107	1	O2	7	7.4%	41
Va′	95	1	L4	0	0.0%	90
TR1.21	108	1	O2	4	4.2%	92
HAU	108	1	O2	6	6.3%	123
HK102	95	1	L12(1)	0	0.0%	9
H20C3K	108	1	L12(2)	3	3.2%	125
CHEB	108	1	O2	7	7.4%	5
HK134	95	1	L15(2)	0	0.0%	10
TEL9	108	1	O2	9	9.5%	73
TR1.32	103	1	O2	3	3.2%	92
RF-KES1	97	1	A20	4	4.2%	121
WES	108	1	L5	10	10.5%	61
DILp1	95	1	O4	1	1.1%	70
SA-4B	107	1	L12(2)	8	8.4%	120
HK101	95	1	L15(1)	0	0.0%	9
TR1.23	108	1	O2	5	5.3%	92
HF2-1/17	108	1	A30	0	0.0%	4
2E7	108	1	A30	1	1.1%	62
33.C9	107	1	L12(2)	7	7.4%	126
3D6	105	1	L12(2)	2	2.1%	34
I-2a	108	1	L8	8	8.4%	70
RF-KL1	97	1	L8	4	4.2%	121
TNF-E7	108	1	A30	9	9.5%	41
TR1.22	108	1	O2	7	7.4%	92
HIV-B35	106	1	O2	2	2.2%	8
HIV-b22	106	1	O2	2	2.2%	8
HIV-b27	106	1	O2	2	2.2%	8
HIV-B8	107	1	O2	10	10.8%	8
HIV-b8	107	1	O2	10	10.8%	8
RF-SJ5	95	1	A30	5	5.3%	113
GAL(1)	108	1	A30	6	6.3%	64
R3.5H5G	108	1	O2	6	6.3%	70
HIV-b14	106	1	A20	2	2.2%	8
TNF-E1	105	1	L5	8	8.4%	41
WEA	108	1	A30	8	8.4%	37
EU	108	1	L12(2)	5	5.3%	40
FOG1-G8	108	1	L8	11	11.6%	41
1X7RG1	108	1	L1	8	8.4%	70
BLI	108	1	L8	3	3.2%	72
KUE	108	1	L12(2)	11	11.6%	32
LUNm01	108	1	L12(2)	10	10.5%	6
HIV-b1	106	1	A20	4	4.3%	8
HIV-s4	103	1	O2	2	2.2%	8
CAR	107	1	L12(2)	11	11.7%	79
BR	107	1	L12(2)	11	11.6%	50
CLL PATIENT 10	88	1	O2	0	0.0%	122
CLL PATIENT 12	88	1	O2	0	0.0%	122
KING	108	1	L12(2)	12	12.6%	30
V13	95	1	L24	0	0.0%	46
CLL PATIENT 11	87	1	O2	0	0.0%	122
CLL PATIENT 13	87	1	O2	0	0.0%	122
CLL PATIENT 9	88	1	O12	1	1.1%	122
HIV-B2	106	1	A20	9	9.7%	8
HIV-b2	106	1	A20	9	9.7%	8
CLL PATIENT 5	88	1	A20	1	1.1%	122
CLL PATIENT 1	88	1	L8	2	2.3%	122
CLL PATIENT 2	88	1	L8	0	0.0%	122
CLL PATIENT 7	88	1	L5	0	0.0%	122
CLL PATIENT 8	88	1	L5	0	0.0%	122
HIV-b5	105	1	L5	11	12.0%	8
CLL PATIENT 3	87	1	L8	1	1.1%	122
CLL PATIENT 4	88	1	L9	0	0.0%	122
CLL PATIENT 18	85	1	L9	6	7.1%	122
CLL PATIENT 17	86	1	L12(2)	7	8.1%	122
HIV-b20	107	3	A27	11	11.7%	8
2C12	108	1	L12(2)	20	21.1%	68
1B11	108	1	L12(2)	20	21.1%	68
1H1	108	1	L12(2)	21	22.1%	68
2A12	108	1	L12(2)	21	22.1%	68
CUR	109	3	A27	0	0.0%	66
GLO	109	3	A27	0	0.0%	16
RF-TS1	96	3	A27	0	0.0%	121
GAR′	109	3	A27	0	0.0%	67
FLO	109	3	A27	0	0.0%	66
PIE	109	3	A27	0	0.0%	91
HAH 14.1	109	3	A27	1	1.0%	51
HAH 14.2	109	3	A27	1	1.0%	51
HAH 16.1	109	3	A27	1	1.0%	51
NOV	109	3	A27	1	1.0%	52
33.F12	108	3	A27	1	1.0%	126
8E10	110	3	A27	1	1.0%	25
TH3	109	3	A27	1	1.0%	25
HIC(R)	108	3	A27	0	0.0%	51
SON	110	3	A27	1	1.0%	67
PAY	109	3	A27	1	1.0%	66
GOT	109	3	A27	1	1.0%	67
mAbA6H4C5	109	3	A27	1	1.0%	12
BOR′	109	3	A27	2	2.1%	84
RF-SJ3	96	3	A27	2	2.1%	121
SIE	109	3	A27	2	2.1%	15
ESC	109	3	A27	2	2.1%	98
HEW′	110	3	A27	2	2.1%	98
YES8c	109	3	A27	3	3.1%	33
TI	109	3	A27	3	3.1%	114
mAb113	109	3	A27	3	3.1%	71
HEW	107	3	A27	0	0.0%	94
BRO	106	3	A27	0	0.0%	94
ROB	106	3	A27	0	0.0%	94
NG9	96	3	A27	4	4.2%	11
NEU	109	3	A27	4	4.2%	66
WOL	109	3	A27	4	4.2%	2
35G6	109	3	A27	4	4.2%	59
RF-SJ4	109	3	A11	0	0.0%	88
KAS	109	3	A27	4	4.2%	84
BRA	106	3	A27	1	1.1%	94
HAH	106	3	A27	1	1.1%	94
HIC	105	3	A27	0	0.0%	94
FS-2	109	3	A27	6	6.3%	87
JH′	107	3	A27	6	6.3%	38
EV1-15	109	3	A27	6	6.3%	83
SCA	108	3	A27	6	6.3%	65
mAb112	109	3	A27	6	6.3%	71
SIC	103	3	A27	3	3.3%	94
SA-4A	109	3	A27	6	6.3%	120
SER	108	3	A27	6	6.3%	98
GOL′	109	3	A27	7	7.3%	82
BSG10K	105	3	A27	9	9.7%	125
HG2B10K	110	3	A27	9	9.4%	125
Taykv322	105	3	A27	5	5.4%	52
CLL PATIENT 24	89	3	A27	1	1.1%	122
HIV-b24	107	3	A27	7	7.4%	8
HIV-b6	107	3	A27	7	7.4%	8
Taykv310	99	3	A27	1	1.1%	52
KA3D1	108	3	L6	0	0.0%	85
19.E7	107	3	L6	0	0.0%	126
rsv61	109	3	A27	12	12.5%	7
Taykv320	98	3	A27	1	1.2%	52
Vh	96	3	L10(2)	0	0.0%	89
LS8	108	3	L6	1	1.1%	109
LS1	108	3	L6	1	1.1%	109
LS2S3-3	107	3	L6	2	2.1%	99
LS2	108	3	L6	1	1.1%	109
LS7	108	3	L6	1	1.1%	109
LS2S3-4d	107	3	L6	2	2.1%	99
LS2S3-4a	107	3	L6	2	2.1%	99
LS4	108	3	L6	1	1.1%	109
LS6	108	3	L6	1	1.1%	109
LS2S3-10a	107	3	L6	2	2.1%	99
LS2S3-8c	107	3	L6	2	2.1%	99
LS5	108	3	L6	1	1.1%	109
LS2S3-5	107	3	L6	3	3.2%	99
LUNm03	109	3	A27	13	13.5%	6
IARC/BL41	108	3	A27	13	13.7%	55
slkv22	99	3	A27	3	3.5%	13
POP	108	3	L6	4	4.2%	111
LS2S3-10b	107	3	L6	3	3.2%	99
LS2S3-8f	107	3	L6	3	3.2%	99
LS2S3-12	107	3	L6	3	3.2%	99
HIV-B30	107	3	A27	11	11.7%	8
HIV-B20	107	3	A27	11	11.7%	8
HIV-b3	108	3	A27	11	11.7%	8
HIV-s6	104	3	A27	9	9.9%	8
YSE	107	3	L2/L16	1	1.1%	72
POM	109	3	L2/L16	9	9.4%	53
Humkv328	95	3	L2/L16	1	1.1%	19
CLL	109	3	L2/L16	3	3.2%	47
LES	96	3	L2/L16	3	3.2%	38
HIV-s5	104	3	A27	11	12.1%	8
HIV-s7	104	3	A27	11	12.1%	8
slkv1	99	3	A27	7	8.1%	13
Humka31es	95	3	L2/L16	4	4.2%	18
slkv12	101	3	A27	8	9.2%	13
RF-TS2	95	3	L2/L16	3	3.2%	121
II-1	109	3	L2/L16	4	4.2%	70
HIV-s3	105	3	A27	13	14.3%	8
RF-TMC1	96	3	L6	10	10.5%	121
GER	109	3	L2/L16	7	7.4%	75
GF4/1.1	109	3	L2/L16	8	8.4%	36
mAb114	109	3	L2/L16	6	6.3%	71
HIV-loop13	109	3	L2/L16	7	7.4%	8
bkv16	86	3	L6	1	1.2%	13
CLL PATIENT 29	86	3	L6	1	1.2%	122
slkv9	98	3	L6	3	3.5%	13
bkv17	99	3	L6	1	1.2%	13
slkv14	99	3	L6	1	1.2%	13
slkv16	101	3	L6	2	2.3%	13
bkv33	101	3	L6	4	4.7%	13
slkv15	99	3	L6	2	2.3%	13
bkv6	100	3	L6	3	3.5%	13
R6B8K	108	3	L2/L16	12	12.6%	125
AL 700	107	3	L2/L16	9	9.5%	117
slkv11	100	3	L2/L16	3	3.5%	13
slkv4	97	3	L6	4	4.8%	13
CLL PATIENT 26	87	3	L2/L16	1	1.1%	122
AL Se124	103	3	L2/L16	9	9.5%	117
slkv13	100	3	L2/116	6	7.0%	13
bkv7	100	3	L2/L16	5	5.8%	13
bkv22	100	3	L2/L16	6	7.0%	13
CLL PATIENT 27	84	3	L2/L16	0	0.0%	122
bkv35	100	3	L6	8	9.3%	13
CLL PATIENT 25	87	3	L2/L16	4	4.6%	122
slkv3	86	3	L2/L16	7	8.1%	13
slkv7	99	1	O2	7	8.1%	13
HuFd79	111	3	L2/L16	24	24.2%	21
RAD	99	3	A27	9	10.3%	78
CLL PATIENT 28	83	3	L2/L16	4	4.8%	122
REE	104	3	L2/L16	25	27.2%	95
FR4	99	3	A27	8	9.2%	77
MD3.3	92	3	L6	1	1.3%	54
MD3.1	92	3	L6	0	0.0%	54
GA3.6	92	3	L6	2	2.6%	54
M3.5N	92	3	L6	3	3.8%	54
WEI′	82	3	A27	0	0.0%	65
MD3.4	92	3	L2/L16	1	1.3%	54
MD3.2	91	3	L6	3	3.8%	54
VER	97	3	A27	19	22.4%	20
CLL PATIENT 30	78	3	L6	3	3.8%	122
M3.1N	92	3	L2/L16	1	1.3%	54
MD3.6	91	3	L2/L16	0	0.0%	54
MD3.8	91	3	L2/L16	0	0.0%	54
GA3.4	92	3	L6	7	9.0%	54
M3.6N	92	3	A27	0	0.0%	54
MD3.10	92	3	A27	0	0.0%	54
MD3.13	91	3	A27	0	0.0%	54
MD3.7	93	3	A27	0	0.0%	54
MD3.9	93	3	A27	0	0.0%	54
GA3.1	93	3	A27	6	7.6%	54
bkv32	101	3	A27	5	5.7%	13
GA3.5	93	3	A27	5	6.3%	54
GA3.7	92	3	A27	7	8.9%	54
MD3.12	92	3	A27	2	2.5%	54
M3.2N	90	3	L6	6	7.8%	54
MD3.5	92	3	A27	1	1.3%	54
M3.4N	91	3	L2/L16	8	10.3%	54
M3.8N	91	3	L2/116	7	9.0%	54
M3.7N	92	3	A27	3	3.8%	54
GA3.2	92	3	A27	9	11.4%	54
GA3.8	93	3	A27	4	5.1%	54
GA3.3	92	3	A27	8	10.1%	54
M3.3N	92	3	A27	5	6.3%	54
B6	83	3	A27	8	11.3%	78
E29.1 KAPPA	78	3	L2/L16	0	0.0%	22
SCW	108	1	O8	12	12.6%	31
REI-based CAMPATH-9	107	1	O8	14	14.7%	39
RZ	107	1	O8	14	14.7%	50
B1	108	1	O8	14	14.7%	14
AND	107	1	O2	13	13.7%	69
2A4	109	1	O2	12	12.6%	23
KA	108	1	O8	19	20.0%	107
MEV	109	1	O2	14	14.7%	29
DEE	106	1	O2	13	14.0%	76
OU(IOC)	108	1	O2	18	18.9%	60
HuRSV19VK	111	1	O8	21	21.0%	115
SP2	108	1	O2	17	17.9%	93
BJ26	99	1	O8	21	24.1%	1
N1	112	1	O8	24	24.2%	106
BMA O310EUC|V2	106	1	L12(1)	21	22.3%	105
CLL PATIENT 6	71	1	A20	0	0.0%	122
BJ19	85	1	O8	16	21.9%	1
GM 607	113	2	A3	0	0.0%	58
R5A3K	114	2	A3	1	1.0%	125
R1C8K	114	2	A3	1	1.0%	125
VK2.R149	113	2	A3	2	2.0%	118
TR1.6	109	2	A3	4	4.0%	92
TR1.37	104	2	A3	5	5.0%	92
FS-1	113	2	A3	6	6.0%	87
TR1.8	110	2	A3	6	6.0%	92
NIM	113	2	A3	8	8.0%	28
Inc	112	2	A3	11	11.0%	35
TEW	107	2	A3	6	6.4%	96
CUM	114	2	O1	7	6.9%	44
HRF1	71	2	A3	4	5.6%	124
CLL PATIENT 19	87	2	A3	0	0.0%	122
CLL PATIENT 20	87	2	A3	0	0.0%	122
Mu	112	2	A3	16	16.2%	26
FR	113	2	A3	20	20.0%	101
MAL-Urine	83	1	O2	6	8.6%	102
Taykv306	73	3	A27	1	1.6%	52
Taykv312	75	3	A27	1	1.6%	52
HIV-b29	93	3	A27	14	17.5%	8
1-185-37	110	3	A27	0	0.0%	119
1-187-29	110	3	A27	0	0.0%	119
TT117	110	3	A27	9	9.4%	63
HIV-loop8	108	3	A27	16	16.8%	8
rsv23L	108	3	A27	16	16.8%	7
HIV-b7	107	3	A27	14	14.9%	8
HIV-b11	107	3	A27	15	16.0%	8
HIV-LC1	107	3	A27	19	20.2%	8
HIV-LC7	107	3	A27	20	21.3%	8
HIV-LC22	107	3	A27	21	22.3%	8
HIV-LC13	107	3	A27	21	22.3%	8
HIV-LC3	107	3	A27	21	22.3%	8
HIV-LC5	107	3	A27	21	22.3%	8
HIV-LC28	107	3	A27	21	22.3%	8
HIV-b4	107	3	A27	22	23.4%	8
CLL PATIENT 31	87	3	A27	15	17.2%	122
HIV-loop2	108	3	L2/L16	17	17.9%	8
HIV-loop35	108	3	L2/116	17	17.9%	8
HIV-LC11	107	3	A27	23	24.5%	8
HIV-LC24	107	3	A27	23	24.5%	8
HIV-b12	107	3	A27	24	25.5%	8
HIV-LC25	107	3	A27	24	25.5%	8
HIV-b21	107	3	A27	24	25.5%	8
HIV-LC26	107	3	A27	26	27.7%	8
G3D10k	108	1	L12(2)	12	12.6%	125
TT125	108	1	L5	8	8.4%	63
HIV-s2	103	3	A27	28	31.1%	8
265-695	108	1	L5	7	7.4%	3
2-115-19	108	1	A30	2	2.1%	119
rsv13L	107	1	O2	20	21.1%	7
HIV-b18	106	1	O2	14	15.1%	8
RF-KL5	98	3	L6	36	36.7%	97
ZM1-1	113	2	A17	7	7.0%	3
HIV-s8	103	1	O8	16	17.8%	8
K-EV15	95	5	B2	0	0.0%	112
RF-TS3	100	2	A23	0	0.0%	121
HF-21/28	111	2	A17	1	1.0%	17
RPMI6410	113	2	A17	1	1.0%	42
JC11	113	2	A17	1	1.0%	49
O-81	114	2	A17	5	5.0%	45
FK-001	113	4	B3	0	0.0%	81
CD5+.28	101	4	B3	1	1.0%	27
LEN	114	4	B3	1	1.0%	104
UC	114	4	B3	1	1.0%	111
CD5+.5	101	4	B3	1	1.0%	27
CD5+.26	101	4	B3	1	1.0%	27
CD5+.12	101	4	B3	2	2.0%	27
CD5+.23	101	4	B3	2	2.0%	27
CD5+.7	101	4	B3	2	2.0%	27
VJI	113	4	B3	3	3.0%	56
LOC	113	4	B3	3	3.0%	72
MAL	113	4	B3	3	3.0%	72
CD5+.6	101	4	B3	3	3.0%	27
H2F	113	4	B3	3	3.0%	70
PB17IV	114	4	B3	4	4.0%	74
CD5+.27	101	4	B3	4	4.0%	27
CD5+.9	101	4	B3	4	4.0%	27
CD5−.28	101	4	B3	5	5.0%	27
CD5−.26	101	4	B3	6	5.9%	27
CD5+.24	101	4	B3	6	5.9%	27
CD5+.10	101	4	B3	6	5.9%	27
CD5−.19	101	4	B3	6	5.9%	27
CD5−.18	101	4	B3	7	6.9%	27
CD5−.16	101	4	B3	8	7.9%	27
CD5−.24	101	4	B3	8	7.9%	27
CD5−.17	101	4	B3	10	9.9%	27
MD4.1	92	4	B3	0	0.0%	54
MD4.4	92	4	B3	0	0.0%	54
MD4.5	92	4	B3	0	0.0%	54
MD4.6	92	4	B3	0	0.0%	54
MD4.7	92	4	B3	0	0.0%	54
MD4.2	92	4	B3	1	1.3%	54
MD4.3	92	4	B3	5	6.3%	54
CLL PATIENT 22	87	2	A17	2	2.3%	122
CLL PATIENT 23	84	2	A17	2	2.4%	122

[0223]

TABLE 2B
rearranged human lambda sequences
		Computed	Germline	Diff. to	% diff. to
Name1	aa2	family3	gene4	germline5	germline6	Reference7
WAH	110	1	DPL3	7	7%	68
1B9/F2	112	1	DPL3	7	7%	9
DIA	112	1	DPL2	7	7%	36
mAb67	89	1	DPL3	0	0%	29
HiH2	110	1	DPL3	12	11%	3
NIG-77	112	1	DPL2	9	9%	72
OKA	112	1	DPL2	7	7%	84
KOL	112	1	DPL2	12	11%	40
T2:C5	111	1	DPL5	0	0%	6
T2:C14	110	1	DPL5	0	0%	6
PR-TS1	110	1	DPL5	0	0%	55
4G12	111	1	DPL5	1	1%	35
KIM46L	112	1	HUMLV117	0	0%	8
Fog-B	111	1	DPL5	3	3%	31
9F2L	111	1	DPL5	3	3%	79
mAb111	110	1	DPL5	3	3%	48
PHOX15	111	1	DPL5	4	4%	49
BL2	111	1	DPL5	4	4%	74
NIG-64	111	1	DPL5	4	4%	72
RF-SJ2	100	1	DPL5	6	6%	78
AL EZI	112	1	DPL5	7	7%	41
ZIM	112	1	HUMLV117	7	7%	18
RF-SJ1	100	1	DPL5	9	9%	78
IGLV1.1	98	1	DPL4	0	0%	1
NEW	112	1	HUMLV117	11	10%	42
CB-201	87	1	DPL2	1	1%	62
MEM	109	1	DPL2	6	6%	50
H210	111	2	DPL10	4	4%	45
NOV	110	2	DPL10	8	8%	25
NEI	111	2	DPL10	8	8%	24
ALMC	110	2	DPL11	6	6%	28
MES	112	2	DPL11	8	8%	84
FOG1-A3	111	2	DPL11	9	9%	27
AL NOV	112	2	DPL11	7	7%	28
HMST-1	110	2	DPL11	4	4%	82
HBW4-1	108	2	DPL12	9	9%	52
WH	110	2	DPL11	11	11%	34
11-50	110	2	DPL11	7	7%	82
HBp2	110	2	DPL12	8	8%	3
NIG-84	113	2	DPL11	12	11%	73
VIL	112	2	DPL11	9	9%	58
TRO	111	2	DPL12	10	10%	61
ES492	108	2	DPL11	15	15%	76
mAb216	89	2	DPL12	1	1%	7
BSA3	109	3	DPL16	0	0%	49
THY-29	110	3	DPL16	0	0%	27
PR-TS2	108	3	DPL16	0	0%	55
E29.1 LAMBDA	107	3	DPL16	1	1%	13
mAb63	109	3	DPL16	2	2%	29
TEL14	110	3	DPL16	6	6%	49
6H-3C4	108	3	DPL16	7	7%	39
SH	109	3	DPL16	7	7%	70
AL GIL	109	3	DPL16	8	8%	23
H6-3C4	108	3	DPL16	8	8%	83
V-lambda-2.DS	111	2	DPL11	3	3%	15
8.12 ID	110	2	DPL11	3	3%	81
DSC	111	2	DPL11	3	3%	56
PV11	110	2	DPL11	1	1%	56
33.H11	110	2	DPL11	4	4%	81
AS17	111	2	DPL11	7	7%	56
SD6	110	2	DPL11	7	7%	56
KS3	110	2	DPL11	9	9%	56
PV6	110	2	DPL12	5	5%	56
NGD9	110	2	DPL11	7	7%	56
MUC1-1	111	2	DPL11	11	10%	27
A30c	111	2	DPL10	6	6%	56
KS6	110	2	DPL12	6	6%	56
TEL13	111	2	DPL11	11	10%	49
AS7	110	2	DPL12	6	6%	56
MCG	112	2	DPL12	12	11%	20
U266L	110	2	DPL12	13	12%	77
PR-SJ2	110	2	DPL12	14	13%	55
BOH	112	2	DPL12	11	10%	37
TOG	111	2	DPL11	19	18%	53
TEL16	111	2	DPL11	19	18%	49
No.13	110	2	DPL10	14	13%	52
BO	112	2	DPL12	18	17%	80
WIN	112	2	DPL12	17	16%	11
BUR	104	2	DPL12	15	15%	46
NIG-58	110	2	DPL12	20	19%	69
WEIR	112	2	DPL11	26	25%	21
THY-32	111	1	DPL8	8	8%	27
TNF-H9G1	111	1	DPL8	9	9%	27
mAb61	111	1	DPL3	1	1%	29
LV1L1	98	1	DPL2	0	0%	54
HA	113	1	DPL3	14	13%	63
LA1L1	111	1	DPL2	3	3%	54
RHE	112	1	DPL1	17	16%	22
K1B12L	113	1	DPL8	17	16%	79
LOC	113	1	DPL2	15	14%	84
NIG-51	112	1	DPL2	12	11%	67
NEWM	104	1	DPL8	23	22%	10
MD3-4	106	3	DPL23	14	13%	4
COX	112	1	DPL2	13	12%	84
HiH10	106	3	DPL23	13	12%	3
VOR	112	1	DPL2	16	15%	16
AL POL	113	1	DPL2	16	15%	57
CD4-74	111	1	DPL2	19	18%	27
AMYLOID MOL	102	3	DPL23	15	15%	30
OST577	108	3	Humlv318	10	10%	4
NIG-48	113	1	DPL3	42	40%	66
CARR	108	3	DPL23	18	17%	19
mAb60	108	3	DPL23	14	13%	29
NIG-68	99	3	DPL23	25	26%	32
KERN	107	3	DPL23	26	25%	59
ANT	106	3	DPL23	17	16%	19
LEE	110	3	DPL23	18	17%	85
CLE	94	3	DPL23	17	17%	19
VL8	98	8	DPL21	0	0%	81
MOT	110	3	Humlv318	23	22%	38
GAR	108	3	DPL23	26	25%	33
32.B9	98	8	DPL21	5	5%	81
PUG	108	3	Humlv318	24	23%	19
T1	115	8	HUMLV801	52	50%	6
RF-TS7	96	7	DPL18	4	4%	60
YM-1	116	8	HUMLV801	51	49%	75
K6H6	112	8	HUMLV801	20	19%	44
K5C7	112	8	HUMLV801	20	19%	44
K5B8	112	8	HUMLV801	20	19%	44
K5G5	112	8	HUMLV801	20	19%	44
K4B8	112	8	HUMLV801	19	18%	44
K6F5	112	8	HUMLV801	17	16%	44
HIL	108	3	DPL23	22	21%	47
KIR	109	3	DPL23	20	19%	19
CAP	109	3	DPL23	19	18%	84
1B8	110	3	DPL23	22	21%	43
SHO	108	3	DPL23	19	18%	19
HAN	108	3	DPL23	20	19%	19
cML23	96	3	DPL2J	3	3%	12
PR-SJ1	96	3	DPL23	7	7%	55
BAU	107	3	DPL23	9	9%	5
TEX	99	3	DPL23	8	8%	19
X(PET)	107	3	DPL23	9	9%	51
DOY	106	3	DPL23	9	9%	19
COT	106	3	DPL23	13	12%	19
Pag-1	111	3	Humlv318	5	5%	31
DIS	107	3	Humlv318	2	2%	19
WIT	108	3	Humlv318	7	7%	19
I.RH	108	3	Humlv318	12	11%	19
S1-1	108	3	Humlv318	12	11%	52
DEL	108	3	Humlv318	14	13%	17
TYR	108	3	Humlv318	11	10%	19
J.RH	109	3	Humlv318	13	12%	19
THO	112	2	DPL13	38	36%	26
LBV	113	1	DPL3	38	36%	2
WLT	112	1	DPL3	33	31%	14
SUT	112	2	DPL12	37	35%	65