US 6,262,216 B1Grant
Functionalized silicon compounds and methods for their synthesis and use
Issue Date:2001-07-17
•16 Claims
•11 Drawing Sheets
Abstract
Provided are functionalized silicon compounds and methods for their synthesis and use. The functionalized silicon compounds include at least one activated silicon group and at least one derivatizable functional group. Exemplary derivatizable functional groups include hydroxyl, amino, carboxyl and thiol, as well as modified forms thereof, such as activated or protected forms. The functionalized silicon compounds may be covalently attached to surfaces to form functionalized surfaces which may be used in a wide range of different applications. In one embodiment, the silicon compounds are attached to the surface of a substrate comprising silica, such as a glass substrate, to provide a functionalized surface on the substrate, to which molecules, including polypeptides and nucleic acids, may be attached. In one embodiment, after covalent attachment of a functionalized silicon compound to the surface of a solid silica substrate to form a functionalized coating on the substrate, an array of nucleic acids may be covalently attached to the substrate. Thus, the method permits the formation of high density arrays of nucleic acids immobilized on a substrate, which may be used, for example, in conducting high volume nucleic acid hybridization assays.
Metadata
Assignee
- Affymetrix, Inc.
Inventor
- Glenn McGall
Application Information
Application Number:US 09/172,190
Filing Date:1998-10-13
Priority Date:1998-10-13
Art Unit:7
Classifications
IPC:
C08G 7700C08G 7704G01N 1506G01N 3300
Field of Search:
528 10528 25528 28528 33422 50422 681
Patent Drawings (11 sheets)
Description
TECHNICAL FIELD
[0002] This application relates to silicon compounds, methods of making silicon compounds, and methods for use of silicon compounds as silyating agents in the treatment of surfaces, such as glass.
BACKGROUND ART
[0003] Silylating agents have been developed in the art which react with and coat surfaces, such as silica surfaces. For example, silylating agents for use in modifying silica used in high performance chromatography packings have been developed. Monofunctional silylating agents have been used to form monolayer surface coatings, while di- and tri-functional silylating agents have been used to form polymerized coatings on silica surfaces. Many silylating agents, however, produce coatings with undesirable properties including instability to hydrolysis and the inadequate ability to mask the silica surface which may contain residual acidic silanols.
[0004] Silylating agents have been developed for the silylation of solid substrates, such as glass substrates, that include functional groups that may be derivatized by further covalent reaction. The silylating agents have been immobilized on the surface of substrates, such as glass, and used to prepare high density immobilized oligonucleotide probe arrays. For example, N-(3-(triethoxysilyl)-propyl)-4-hydroxybutyramide (PCR Inc., Gainesville, Fla.) has been used to silylate a glass substrate prior to photochemical synthesis of arrays of oligonucleotides on the substrate, as described in McGall et al., J Am. Chem. Soc.,119:5081-5090 (1997), the disclosure of which is incorporated herein by reference.
[0005] Hydroxyalkylsilyl compounds that have been used to prepare hydroxyalkylated substances, such as glass substrates. N,N-bis(hydroxyethyl) aminopropyl-triethoxysilane has been used to treat glass substrates to permit the synthesis of high-density oligonucleotide arrays. McGall et al., Proc. Nati. Acad Sci.,93:13555-13560 (1996); and Pease et al., Proc. Natl. Acad. Sci.,91:5022-5026 (1994), the disclosures of which are incorporated herein. Acetoxypropyl-triethoxysilane has been used to treat glass substrates to prepare them for oligonucleotide array synthesis, as described in PCT WO 97/39151, the disclosure of which is incorporated herein. 3-Glycidoxy propyltrimethoxysilane has been used to treat a glass support to provide a linker for the synthesis of oligonucleotides. EP Patent Application No. 89 120696.3.
[0006] Methods have been developed in the art for stabilizing surface bonded silicon compounds. The use of sterically hindered silylating agents is described in Kirkland et al., Anal. Chem.61:2-11 (1989); and Schneider et al., Synthesis,1027-1031 (1990). However, the use of these surface bonded silylating agents is disadvantageous, because they typically require very forcing conditions to achieve bonding to the glass, since their hindered nature makes them less reactive with the substrate.
[0007] It is an object of the invention to provide functionalized silicon compounds that are provided with derivatizable functional groups, that can be used to form functionalized coatings on materials, such as glass. It is a further object of the invention to provide functionalized silicon compounds that can be used to form coatings on materials that are stable under the conditions of use.
DISCLOSURE OF THE INVENTION
[0008] Provided are functionalized silicon compounds and methods for their use. The functionalized silicon compounds include an activated silicon group and a derivatizable functional group. Exemplary derivatizable functional groups include hydroxyl, amino, carboxyl and thiol, as well as modified forms thereof, such as activated or protected forms. The functionalized silicon compounds may be covalently attached to surfaces to form functionalized surfaces which may be used in a wide range of different applications. In one embodiment, the silicon compounds are attached to the surface of a substrate comprising silica, such as a glass substrate, to provide a functionalized surface on the silica containing substrate, to which molecules, including polypeptides and nucleic acids, may be attached. In one preferred embodiment, after covalent attachment of a functionalized silicon compound to the surface of a solid silica substrate to form a functionalized coating on the substrate, an array of nucleic acids may be covalently attached to the substrate. Thus, the method permits the formation of high density arrays of nucleic acids immobilized on a substrate, which may be used in conducting high volume nucleic acid hybridization assays.
BRIEF DESCRIPTION OF THE DRAWINGS
[0009] FIG. 1 shows the structure of the functionalized silicon compounds VI and VII and compounds of Formula 6a
[0010] FIG. 2 shows the structure of the functionalized silicon compound VIII.
[0011] FIG. 3 shows schemes for the synthesis of compounds IX and X.
[0012] FIG. 4 is a scheme showing the synthesis of compounds of Formula 5 or 6.
[0013] FIG. 5 show schemes for the synthesis of compounds XII, XIII and compounds of Formula 8.
[0014] FIG. 6 shows schemes for the synthesis of compounds XV, VI and compounds of Formula 9.
[0015] FIG. 7 shows schemes showing the synthesis of compounds of Formula 10 or 11.
[0016] FIG. 8 shows schemes showing the synthesis of compounds of Formula 12 or 3.
[0017] FIG. 9 is a scheme of the synthesis of compounds of Formula 16b.
[0018] FIG. 10 illustrates the structure of compounds of Formula 14 and 15.
[0019] FIG. 11 is a graph of stability of silicon compound bonded phases vs. time.
[0020] FIG. 12 is a graph of surface fluorescence intensity vs. silane that illustrates comparative stability of surface bonded silicon compounds.
MODES FOR CARRYING OUT THE INVENTION
[0021] Functionalized silicon compounds are provided, as well as methods for their synthesis and use. The functionalized silicon compounds may be used to form functionalized coatings on a variety of surfaces such as the surfaces of glass substrates.
FUNCTIONALIZED SILICON COMPOUNDS
[0022] A variety of functionalized silicon compounds, which are available commercially, or which may be synthesized as disclosed herein, may be used in the methods disclosed herein to react with surfaces to form functionalized surfaces which may be used in a wide range of different applications. In one embodiment, the functionalized silicon compounds are covalently attached to surfaces to produce functionalized surfaces on substrates. For example, the silicon compounds may be attached to the surfaces of glass substrates, to provide a functionalized surface to which molecules, including polypeptides and nucleic acids, may be attached.
[0023] As used herein, the term “silicon compound” refers to a compound comprising a silicon atom. In a preferred embodiment, the silicon compound is a silylating agent comprising an activated silicon group, wherein the activated silicon group comprises a silicon atom covalently linked to at least one reactive group, such as an alkoxy or halide, such that the silicon group is capable of reacting with a functional group, for example on a surface of a substrate, to form a covalent bond with the surface. For example, the activated silicon group on the silicon compound can react with the surface of a silica substrate comprising surface Si—OH groups to create siloxane bonds between the silicon compound and the silica substrate. Exemplary activated silicon groups include —Si(OMe)3; —SiMe(OMe)2; —SiMeCl2; SiMe(OEt)2; SiCl3and —Si(OEt)3.
[0024] As used herein, the term “functionalized silicon compound” refers to a silicon compound comprising a silicon atom and a derivatizable functional group. In a preferred embodiment, the functionalized silicon compound is a functionalized silylating agent and includes an activated silicon group and a derivatizable functional group. As used herein, the term “derivatizable functional group” refers to a functional group that is capable of reacting to permit the formation of a covalent bond between the silicon compound and another substance, such as a polymer. Exemplary derivatizable functional groups include hydroxyl, amino, carboxyl and thiol, as well as modified forms thereof, such as activated or protected forms. Derivatizable functional groups also include substitutable leaving groups such as halo or sulfonate. In one preferred embodiment, the derivatizable functional group is a group, such as a hydroxyl group, that is capable of reacting with activated nucleotides to permit nucleic acid synthesis. For example, the functionalized silicon compound may be covalently attached to the surface of a substrate, such as glass, and then derivatizable hydroxyl groups on the silicon compound may be reacted with an activated phosphate group on a protected nucleotide phosphoramidite or H-phosphonate, and then stepwise addition of further protected nucleotide phosphoramidites or H-phosphonates can result in the formation of a nucleic acid covalently attached to the support. The nucleic acids also may be attached to the derivatizable group via a linker. In a further embodiment, arrays of nucleic acids may be formed covalently attached to the substrate which are useful in conducting nucleic acid hybridization assays.
[0025] The term “polynucleotide” or “nucleic acid” as used herein refers to a polymeric form of nucleotides of any length, either ribonucleotides or deoxyribonucleotides, that comprise purine and pyrimidine bases, or other natural, chemically or biochemically modified, non-natural, or derivatized nucleotide bases. The backbone of the polynucleotide can comprise sugars and phosphate groups, as may typically be found in RNA or DNA, or modified or substituted sugar or phosphate groups. A polynucleotide may comprise modified nucleotides, such as methylated nucleotides and nucleotide analogs. The sequence of nucleotides may be interrupted by non-nucleotide components.
[0026] The functionalized silicon compounds used to form coatings on a surface may be selected, and obtained commercially, or made synthetically, depending on their properties under the conditions of intended use. For example, functionalized silicon compounds may be selected for silanization of a substrate that are stabile after the silylation reaction to hydrolysis.
[0027] For example, in one embodiment, the functionalized silicon compounds are used to form a coating on a solid substrate, and include functional groups that permit the covalent attachment or synthesis of nucleic acid arrays to the solid substrate, such as glass. The resulting substrates are useful in nucleic acid hybridization assays, which are conducted, for example in aqueous buffers. In one embodiment, preferred are silicon compounds that produce coatings that are substantially stable to hybridization assay conditions, such as phosphate or TRIS buffer at about pH 6-9, and at elevated temperatures, for example, about 25-65° C., for about 1 to 72 hours, such that hydrolysis is less than about 90%, e.g., less than about 50%, or e.g, less than about 20%, or about 10%. The functionalized surfaces on the substrate, formed by covalent attachment of functionalized silicon compounds, advantageously are substantially stable to provide a support for biomolecule array synthesis and to be used under rigorous assay conditions, such as nucleic acid hybridization assay conditions.
[0028] The functionalized silicon compound in one embodiment includes at least one activated silicon group and at least one derivatizable functional group. In one embodiment, the functionalized silicon compound includes at least one activated silicon group and a plurality of derivatizable functional groups, for example, 2, 3, 4 or more derivatizable functional groups. In another embodiment, the functionalized silicon compound includes at least one derivatizable functional group and a plurality of activated silicon groups, for example, 2, 3, 4 or more activated silicon groups. Methods of making the functionalized silicon compounds are provided as disclosed wherein, as well as methods of use of the functionalized silicon compounds, including covalent attachment of the silicon compounds to surfaces of substrates to form functionalized surfaces, and further derivation of the surfaces to provide arrays of nucleic acids for use in assays on the surfaces.
[0029] In one embodiment, there is provided a method of functionalizing a surface, the method comprising covalently attaching to the surface a functionalized silicon compound, wherein the functionalized silicon compound comprises at least one derivatizable functional group and a plurality of activated silicon groups, for example, 2, 3, 4 or more activated silicon groups. The method may further comprise covalently attaching a plurality of functionalized silicon compounds to the surface, and forming an array of nucleic acids covalently attached to the functionalized silicon compounds on the surface.
[0030] Exemplary functionalized silicon compounds include compounds of Formula 1 shown below:
[0031] wherein R1and R2are independently a reactive group, such as halide or alkoxy, for example —OCH3or —OCH2CH3, and R3is alkoxy, halide or alkyl; and wherein R4is a hydrophobic and/or sterically hindered group. In the functionalized silylating agents of Formula 1, R4may be alkyl or haloalkyl, for example, —CH3, —CH2CH3, —CH(CH3)2, —C(CH3)3, or —CH(CF3)2. A hydrophobic and/or sterically hindered R4group, such as isopropyl or isobutyl, may be used to increase the hydrolytic stability of the resulting surface layer. Further hydrophobicity may be imparted by the use of a fluorocarbon R4group, such as hexafluoroisopropyl ((CF3)2CH—).
[0032] An exemplary compound of Formula 1 is silicon compound I below:
[0033] In general, silicon compounds provide uniform and reproducible coatings. Silicon compounds with one derivatizable functional group can provide a lower concentration of surface derivatizable functional groups at maximum coverage of the substrate than the silicon compounds including multiple derivatizable functional groups. Silicon compounds with one derivatizable functional group, such as silicon compounds of Formula 1, however, which include a hydrophobic and/or sterically hindered R group, such as isopropyl or isobutyl, are advantageous since the hydrophobic or sterically hindered R group increases the hydrolytic stability of the resulting surface layer.
[0034] In one embodiment the functionalized silicon compounds of Formula 2 are provided:
[0035] In Formula 2, in one embodiment, R1, R2and R3are independently a reactive group, such as alkoxy or halide, for example, —OCH3, or —OCH2CH3, and wherein, in one embodiment, R1, R2and R3are each —OCH3In one embodiment R1and R2are independently a reactive group, such as alkoxy or halide, for example —OCH3or —OCH2CH3, and R3is an alkoxy or halide group or an alkyl group, such as —CH3, or substituted alkyl group.
[0036] In Formula 2, in one embodiment, L1and L2are independently alkyl, preferably —(CH2)n—, wherein n=2 to 10, e.g., 3 to 4, or e.g., 2-3.
[0037] In Formula 2, in one embodiment, A1is H or a moiety comprising one or more derivatizable functional groups. In one embodiment, A1is a moiety comprising an amino group or a hydroxyl group, such as —CH2CH2OH. In another embodiment, A1is, for example, a branched hydrocarbon including a plurality of derivatizable functional groups, such as hydroxyl groups. In one embodiment in Formula 2, A1is:
[0038] wherein p is 1-10, q is 0 or 1, and r is 2-5.
[0039] In one embodiment of Formula 2, R1and R2are independently alkoxy or halide; R3is alkoxy, halide or alkyl; L1and L2are both —(CH2)n—, wherein n=2 to 10, e.g., 2 to 3; and A1is H or a moiety comprising one or more derivatizable functional groups.
[0040] Exemplary compounds of Formula 2 include compounds II, III and IV below. Other silicon compounds of Formula 2 that may be used to form functional surface coatings with enhanced hydrolytic stability include silicon compounds IX and X, shown in FIG. 3. In compound VIII, the triethoxysilyl group is shown by way of example, however alternatively, the activated silicon group may be other activated silicon groups or mixtures thereof, such as trimethoxysilyl. In another embodiment, there is provided a compound of Formula 11, wherein n is, for example, 1 to 10, e.g., 1-3, and G is a derivatizable functional group, such as hydroxyl, protected hydroxyl or halide such as Cl or Br, as shown in FIG. 7.
[0041] In another embodiment, silicon compounds of Formula 14 in FIG. 10 are provided wherein, R1, R2are independently a reactive group such as alkoxy, for example —OCH3or —OCH2CH3, or halide; and R3is a reactive group such as alkoxy or halide, or optionally alkyl.
[0042] In a further embodiment, compounds of Formula 3 are provided:
[0043] In Formula 3, in one embodiment, R1, R2and R3are independently reactive groups, such as alkoxy or halide, for example, —OCH3, or —OCH2CH3, and wherein, in one embodiment, R1, R2and R3are each —OCH3. In one embodiment R1and R2are independently a reactive group, such as alkoxy or halide, for example —OCH3or —OCH2CH3, and R3is an alkoxy or halide group or an alkyl group, such as —CH3, or substituted alkyl group.
[0044] In Formula 3, in one embodiment, L1, L2, and L3are independently a linker, for example, a straight chain saturated hydrocarbon, such as —(CH2)n—, wherein n=1 to 10, or 1 to 5, or, e.g., 2 to 3.
[0045] In Formula 3, in one embodiment, A1and A2are independently H or moieties comprising one or more derivatizable functional groups, such as hydroxyl or amino groups, or modified forms thereof, such as protected forms. In another embodiment, A1and A2each comprise a plurality of derivativizable functional groups. For example, A1and A2may each comprise a branched moiety including a plurality of derivatizable functional groups, such as hydroxyl groups.
[0046] In one embodiment of Formula 3, R1and R2are independently alkoxy or halide; R3is alkoxy, halide or alkyl; L1, L2, and L3are independently —(CH2)n—, wherein n is 2-10; and A1and A2are independently a moiety comprising one or more derivatizable functional groups.
[0047] In another embodiment of Formula 3, A1is —L4—G2, and A2is —L5—G2; R1and R2are independently alkoxy or halide; R3is alkoxy, halide or alkyl; L1, L2, L3, L4and L5are —(CH2)n—, wherein n is 1 to 10, for example 2 to 3; and G1and G2are independently a moiety comprising one or more derivatizable functional groups. In another embodiment, L1, L4, and L5are —(CH2)2—, L2and L3are —(CH2)3—, and G1and G2are —OH.
[0048] In another embodiment, silicon compounds of Formula 15 in FIG. 10 are provided, wherein R1, R2are independently alkoxy, for example —OCH3or —OCH2CH3, or halide; and R3is alkoxy, alkyl, or halide.
[0049] In a further embodiment, compounds of Formula 6a in FIG. 1 are provided, wherein n is 1-3, for example 2 or 3. Exemplary functionalized silicon compounds include compound V below, and compound VI shown in FIG. 1.
[0050] Another embodiment is illustrated in FIG. 7, which shows a compound of Formula 10, wherein n=1 to 10, e.g., 1-3, and G is a derivatizable functional group, such as hydroxyl, protected hydroxyl, or halide such as Cl or Br.
[0051] The hydrolytic stability of the silicon compound coating may be increased by increasing the number of covalent bonds to the surface of the support. For example, silicon compounds II-V include two activated silicon groups for binding to a support surface, such as glass. A variety of functionalized silicon compounds including a plurality of activated silicon groups and derivatizable functional groups are useful to form functionalized coatings. A further example is compound VII shown in FIG. 1. Another example is silicon compound VIII shown in FIG. 2, which can form up to three covalent bonds to the surface of a glass support. In compound VIII, the triethoxysilyl group is shown by way of example, however alternatively, the activated silicon group may be other activated silicon groups or mixtures thereof, such as trimethoxysilyl. Similarly, in all of the silicon compounds disclosed herein in which a representative activated silicon group, such as trimethoxysilyl, is substituted on the compound, the compounds in other embodiments also may be substituted with other activated silicon groups known in the art and disclosed herein.
[0052] The silicon compounds II-VIII having multiple silicon groups enhance potentially by twice as much, or more, the hydrolytic stability in comparison to silicon compounds comprising only a single silicon group, since they possess more trialkoxysilyl groups that can react, and form bonds with, a surface. The number of silicon groups in the silicon compound may be modified for different applications, to increase or decrease the number of bonds to a support such as a glass support. Silcon compounds may be used that form optimally stable surface-bonded films on glass via covalent siloxane bonds. Additionally, the number of derivatizable functional groups may be increased or decreased for different applications, as illustrated by silicon compounds II-VIII. Silicon compounds may be selected for use that provide the desired optimum density of surface derivatizable groups, such as hydroxyalkyl groups, for a desired application, such as the synthesis of nucleic acid arrays, or for the optimum stability during use of the array in different applications.
[0053] Other embodiments of functionalized silicon compounds include compounds XII and XIII shown in FIG. 5, and compound XV shown in FIG. 6.
[0054] In another embodiment, polymeric functionalized silicon compounds of Formula 4 are provided:
[0055] In Formula 4, in one embodiment, x, y and z are independently 1-3 and, in one embodiment, x, y and z are each 2.
[0056] In Formula 4, in one embodiment, L1, L2and L3are independently linkers, for example, straight chain hydrocarbons, and preferably —(CH2)m—, wherein m=1-10, e.g., 2-3.
[0057] In Formula 4, in one embodiment, at least one of A, B and C is —SiR1R2R3, wherein R1and R2are independently a reactive group, such as alkoxy or halide, for example, —OCH3, or —OCH2CH3and R3is alkoxy, halide or alkyl; and wherein the remainder of A, B and C are independently moieties comprising one or more derivatizable functional groups, such as hydroxyl groups, or amino groups, or modified forms thereof, such as protected forms, for example —OH or a branched molecule comprising one or more hydroxyl groups.
[0058] In Formula 4, in one embodiment, n is, for example, about 10 to 10,000, or, for example, about 1,000 to 10,000.
[0059] In one embodiment of Formula 4, B is —SiR1R2R3, wherein R1, R2and R3are independently alkoxy, halide or alkyl; x, y, and z are independently 2-3; L1, L2and L3are independently —(CH2)m—, wherein m is 2-3; A and C are independently moieties comprising derivatizable functional groups; and n is about 10 to 10,000.
[0060] In one embodiment of Formula 4, B is —Si(OCH3)3; x, y, and z are 2; L1and L3are —(CH2)2—; L2is —(CH2)3—; A and C are moieties comprising derivatizable functional groups; and n is about 10 to 10,000.
[0061] Other embodiments of a polymeric functionalized silicon compound include compounds of Formula 5 and 6 shown in FIG. 4, wherein m is about 0 to 10, e.g., about 1 to 5, and n is about 10 to 10,000. In Formulas 5 and 6, R1and R2are independently a reactive group, such as alkoxy or halide, for example, —OCH3or —OCH2CH3, and R3is a reactive group, such as alkoxy or halide, or optionally alkyl, for example —CH3.
[0062] Other embodiments include compounds of Formula 7 and 8, shown in FIG. 5, and Formula 9, shown in FIG. 6, wherein n is about 10 to 10,000. In Formulas 7, 8 and 9, R1and R2are independently a reactive group, such as alkoxy or halide, for example, —OCH3or —OCH2CH3, and R3is a reactive group such as alkoxy or halide or optionally alkyl, for example —CH3.
[0063] Further embodiments include compounds of Formula 12 and 13, shown in FIG. 8, wherein m is about 10 to 10,000, and n is about 1 to 10, e.g., about 5 to 10. In Formulas 12 and 13, R1and R2are independently a reactive group, such as alkoxy or halide, for example, —OCH3or —OCH2CH3, and R3is a reactive group, such as alkoxy or halide, or optionally alkyl, for example —CH3. In Formula 12, G is a substitutable leaving group, such as hydroxy, protected hydroxy, or halo, such as —Cl or —Br.
[0064] The use of a polymer permits the formation of stable films on surfaces, such as glass, due to the very large number of siloxane bonds that can be formed with the surface. The number of alkoxysilicon groups relative to the number of hydroxyalkyl groups can be selected to provide the desired density of reactive hydroxyl groups.
Synthesis of Functionalized Silicon Compounds
[0065] Functionalized silicon compounds for use in the methods described herein are available commercially, or may be synthesized from commercially available starting materials. Commercially available silicon compounds and a review of silicon compounds is provided in Arkles, Ed., “Silicon, Germanium, Tin and Lead Compounds, Metal Alkoxides, Diketonates and Carboxylates, A Survey of Properties and Chemistry,” Gelest, Inc., Tullytown, Pa., 1995, the disclosure of which is incorporated herein. Functionalized silicon compounds may be synthesized using methods available in the art of organic chemistry, for example, as described in March, Advanced Organic Chemistry,John Wiley & Sons, New York, 1985.
[0066] Methods of synthesizing compounds of Formula 1 are shown in Scheme I below. Commercially available reagents which may be used in syntheses in accordance with Scheme I include 3-chloro-1-triethoxysilylpropane and ethylene oxide (Aldrich®, Milwaukee, Wis.).
[0067] A method for the conversion of bis(trimethoxysilylpropyl)amine, XIV, which is commercially available from Gelest, Inc. (Tullytown, Pa.) to compound II is illustrated below in Scheme II.
[0068] A method for the conversion of compound XI, bis[3-trimethoxysilyl)propyl]ethylenediamine, which is commercially available from Gelest, Inc., Tallytown, Pa., to compound V is shown below in Scheme III.
[0069] A method for the synthesis of compound III is shown below in Scheme IV. The reagents shown in Scheme IV are commercially available from Aldrich® (Milwaukee, Wis.).
[0070] Reaction schemes for the synthesis of functionalized silicon compounds IX and X are provided in FIG. 3. Reaction schemes for the synthesis of compounds of Formulas 5 and 6 are shown in FIG. 4. Polyethyleneimine is available commercially, for example, from Aldrich®. Polyamines of Formula 5, where R1, R2and R3are OMe (trimethoxysilylpropyl modified (polyethyleneimine)), or R1is Me and R2and R3are OMe (dimethoxymethylsilylpropyl modified (polyethylenimine)) are available from Gelest (Tullytown, Pa.). FIG. 9 shows another embodiment of a reaction scheme using commercially available reagents, wherein the compound of Formula 16a is converted to the compound of Formula 16b.
[0071] Reaction schemes for the synthesis of compounds XII, XIII, and compounds of Formula 8 are shown in FIG. 5. Synthesis of the reagent, N,N-bis(2-hydroxyethyl) acrylamide is described in U.S. Pat. No. 3,285,886 (1966), the disclosure of which is incorporated herein.
[0072] Reaction schemes for the synthesis of functionalized silicon compounds XV, VI and compounds of Formula 9 are shown in FIG. 6. Use of the reagent N,N-bis (2-hydroxyethyl)-2-chloro-ethylamine is described in Okubo et al., Deutsches Patent 2144759 (1971), the disclosure of which is incorporated herein.
[0073] FIG. 7 illustrates reaction schemes for the synthesis of compounds of Formulas 10 and 11. The use of the reagent, 4-chlorobutanoyl chloride, is described in Njoroge et al., PCT US97/15899 (1998), the disclosure of which is incorporated herein. Other reagents include lactones, such as γ-butyrolactone, δ-valerolactone, and ε-caprolactone (Aldrich®). Compounds XI and XIV are commercially available from Gelest.
[0074] FIG. 8 illustrates reaction schemes for compounds of Formulas 12 and 13. In FIG. 8, G is a substitutable leaving group such as halo. Reagents in addition to those discussed above that may be used in syntheses which may be conducted as shown in FIG. 8 include diethanolamine and N,N-bis(2-hydroxyethyl)glycine, which are commercially available, for example, from Aldrich®.
[0075] Functionalized silicon compounds within the scope of the invention that may be used to form functionalized covalent coatings on surfaces that are useful in a variety of applications and assays further include amine compounds such as compound XI, as well as reaction products formed therefrom as disclosed herein.
Applications
[0076] The methods and compositions disclosed herein may be used in a variety of applications. The functionalized silicon compounds may be covalently attached to a variety of materials, to provide derivatizable functional groups on the materials. Exemplary materials include materials that comprise a functional group that is capable of reacting with the activated silicon group of the silicon compound. For example, the material may comprise a silica material comprising surface silanols capable of reacting with the activated silicon group to form a siloxane bond between the silicon atom on the silicon compound and the silicon atom on the surface. Thus, the functionalized silicon compounds may be attached to, for example, materials comprising silica, such as glass, chromatography material, and solid supports used for solid phase synthesis, such as nucleic acid synthesis. The functionalized silicon compounds further may be attached to materials comprising oxides such as titanium(IV) dioxide and zirconium dioxide, aluminum oxide and indium-tin oxides.
[0077] Solid substrates which may be coated by the silicon compounds include any of a variety of fixed organizational support matrices. In some embodiments, the substrate is substantially planar. In some embodiments, the substrate may be physically separated into regions, for example, with trenches, grooves, wells and the like. Examples of substrates include slides, beads and solid chips. The solid substrates may be, for example, biological, nonbiological, organic, inorganic, or a combination thereof, and may be in forms including particles, strands, gels, sheets, tubing, spheres, containers, capillaries, pads, slices, films, plates, and slides depending upon the intended use.
[0078] The functionalized silicon compounds used advantageously may be selected with selected properties for a particular application. Functionalized silicon compounds may be selected which can form silicon compound surface coatings that have good stability to hydrolysis. Functionalized silicon compounds may be selected which have a selected reactivity with the substrate and a selected derivatizable functional group depending on the intended use.
[0079] In one embodiment, the functionalized silicon compounds may be covalently attached to the surface of a solid substrate to provide a coating comprising derivatizable functional groups on the substrate, thus permitting arrays of immobilized oligomers to be covalently attached to the substrate via covalent reaction with the derivatizable functional groups. The immobilized oligomers, such as polypeptides, or nucleic acids can be used in a variety of binding assays including biological binding assays. In one embodiment, high density arrays of immobilized nucleic acid probes may be formed on the substrate, and then one or more target nucleic acids comprising different target sequences may be screened for binding to the high density array of nucleic acid probes comprising a diversity of different potentially complementary probe sequences. For example, methods for light-directed synthesis of DNA arrays on glass substrates is described in McGall et al, J Am. Chem. Soc.,119:5081-5090 (1997), the disclosure of which is incorporated herein.
[0080] Silanation of glass substrates with the silicon compounds described herein can be conducted, for example by dip-, or spin-application with a 1%-10% solution of silicon compound in an aqueous or organic solvent or mixture thereof, for example in 95% EtOH, followed by thermal curing. See, for example, Arkles, Chemtech,7:766-778 (1997); Leyden, Ed., “Silanes Surfaces and Interfaces, Chemically Modified Surfaces,” Vol. 1, Gordon & Breach Science, 1986; and Plueddemann, E. P., Ed., “Silane Coupling Reagents”, Plenum Pub. Corp., 1991, the disclosures of which are incorporated herein. Methods for screening target molecules for specific binding to arrays of polymers, such as nucleic acids, immobilized on a solid substrate, are disclosed, for example, in U.S. Pat. No. 5,510,270, the disclosure of which is incorporated herein. The fabrication of arrays of polymers, such as nucleic acids, on a solid substrate, and methods of use of the arrays in different assays, are also described in: U.S. Pat. Nos. 5,677,195, 5,624,711, 5,599,695, 5,445,934, 5,451,683, 5,424,186, 5,412,087, 5,405,783, 5,384,261, 5,252,743 and 5,143,854; PCT WO 92/10092; and U.S. application Ser. No. 08/388,321, filed Feb 14, 1995, the disclosures of each of which are incorporated herein. Accessing genetic information using high density DNA arrays is further described in Chee, Science274:610-614 (1996), the disclosure of which is incorporated herein by reference. The combination of photolithographic and fabrication techniques allows each probe sequence to occupy a very small site on the support. The site may be as small as a few microns or even a small molecule. Such probe arrays may be of the type known as Very Large Scale Immobilized Polymer Synthesis (VLSIPS®) arrays, as described in U.S. Pat. No. 5,631,734, the disclosure of which is incorporated herein.
[0081] In the embodiment wherein solid phase chemistry, photolabile protecting groups and photolithography are used to create light directed spatially addressable parallel chemical synthesis of a large array of polynucleotides on the substrate, as described in U.S. Pat. No 5,527,681, the disclosure of which is incorporated herein, computer tools may be used for forming arrays. For example, a computer system may be used to select nucleic acid or other polymer probes on the substrate, and design the layout of the array as described in U.S. Pat. No. 5,571,639, the disclosure of which is incorporated herein.
[0082] Substrates having a surface to which arrays of polynucleotides are attached are referred to herein as “biological chips”. The substrate may be, for example, silicon or glass, and can have the thickness of a microscope slide or glass cover slip. Substrates that are transparent to light are useful when the assay involves optical detection, as described, e.g., in U.S. Pat. No. 5,545,531, the disclosure of which is incorporated herein. Other substrates include Langmuir Blodgett filn, germanium, (poly)tetrafluorethylene, polystyrene, (poly)vinylidenedifluoride, polycarbonate, gallium arsenide, gallium phosphide, silicon oxide, silicon nitride, and combinations thereof In one embodiment, the substrate is a flat glass or single crystal silicon surface with relief features less than about 10 Angstoms.
[0083] The surfaces on the solid substrates will usually, but not always, be composed of the same material as the substrate. Thus, the surface may comprise any number of materials, including polymers, plastics, resins, polysaccharides, silica or silica based materials, carbon, metals, inorganic glasses, membranes, or any of the above-listed substrate materials. Preferably, the surface will contain reactive groups, such as carboxyl, amino, and hydroxyl. In one embodiment, the surface is optically transparent and will have surface Si—OH functionalities such as are found on silica surfaces.
[0084] In the embodiment wherein arrays of nucleic acids are immobilized on a surface, the number of nucleic acid sequences may be selected for different applications, and may be, for example, about 100 or more, or, e.g., in some embodiments, more than 105or 108. In one embodiment, the surface comprises at least 100 probe nucleic acids each preferably having a different sequence, each probe contained in an area of less than about 0.1 cm2, or, for example, between about 1 μm2and 10,000 μm2, and each probe nucleic acid having a defined sequence and location on the surface. In one embodiment, at least 1,000 different nucleic acids are provided on the surface, wherein each nucleic acid is contained within an area less than about 10−3cm2, as described, for example, in U.S. Pat. No. 5,510,270, the disclosure of which is incorporated herein.
[0085] Arrays of nucleic acids for use in gene expression monitoring are described in PCT WO 97/10365, the disclosure of which is incorporated herein. In one embodiment, arrays of nucleic acid probes are immobilized on a surface, wherein the array comprises more than 100 different nucleic acids and wherein each different nucleic acid is localized in a predetermined area of the surface, and the density of the different nucleic acids is greater than about 60 different nucleic acids per 1 cm2.
[0086] Arrays of nucleic acids immobilized on a surface which may be used also are described in detail in U.S. Pat. No. 5,744,305, the disclosure of which is incorporated herein. As disclosed therein, on a substrate, nucleic acids with different sequences are immobilized each in a predefined area on a surface. For example, 10, 50, 60, 100, 103, 104, 105, 106, 107, or 108different monomer sequences may be provided on the substrate. The nucleic acids of a particular sequence are provided within a predefined region of a substrate, having a surface area, for example, of about 1 cm2to 10 −10cm2. In some embodiments, the regions have areas of less than about 10−1, 10−2, 10−3, 10−4, 10−5, 10−6, 10−7, 10−8, 10−9, or 10−10cm2. For example, in one embodiment, there is provided a planar, non-porous support having at least a first surface, and a plurality of different nucleic acids attached to the first surface at a density exceeding about 400 different nucleic acids/cm2, wherein each of the different nucleic acids is attached to the surface of the solid support in a different predefined region, has a different determinable sequence, and is, for example, at least 4 nucleotides in length. The nucleic acids may be, for example, about 4 to 20 nucleotides in length. The number of different nucleic acids may be, for example, 1000 or more. In the embodiment where polynucleotides of a known chemical sequence are synthesized at known locations on a substrate, and binding of a complementary nucleotide is detected, and wherein a fluorescent label is detected, detection may be implemented by directing light to relatively small and precisely known locations on the substrate. For example, the substrate is placed in a microscope detection apparatus for identification of locations where binding takes place. The microscope detection apparatus includes a monochromatic or polychromatic light source for directing light at the substrate, means for detecting fluoresced light from the substrate, and means for determining a location of the fluoresced light. The means for detecting light fluoresced on the substrate may in some embodiments include a photon counter. The means for determining a location of the fluoresced light may include an x/y translation table for the substrate. Translation of the substrate and data collection are recorded and managed by an appropriately programmed digital computer, as described in U.S. Pat. No. 5,510,270, the disclosure of which is incorporated herein.
[0087] Devices for concurrently processing multiple biological chip assays may be used as described in U.S. Pat. No. 5,545,531, the disclosure of which is incorporated herein. Methods and systems for detecting a labeled marker on a sample on a solid support, wherein the labeled material emits radiation at a wavelength that is different from the excitation wavelength, which radiation is collected by collection optics and imaged onto a detector which generates an image of the sample, are disclosed in U.S. Pat. No. 5,578,832, the disclosure of which is incorporated herein. These methods permit a highly sensitive and resolved image to be obtained at high speed. Methods and apparatus for detection of fluorescently labeled materials are further described in U.S. Pat. Nos. 5,631,734 and 5,324,633, the disclosures of which are incorporated herein.
[0088] The methods and compositions described herein may be used in a range of applications including biomedical and genetic research and clinical diagnostics. Arrays of polymers such as nucleic acids may be screened for specific binding to a target, such as a complementary nucleotide, for example, in screening studies for determination of binding affinity and in diagnostic assays. In one embodiment, sequencing of polynucleotides can be conducted, as disclosed in U.S. Pat. No. 5,547,839, the disclosure of which is incorporated herein. The nucleic acid arrays may be used in many other applications including detection of genetic diseases such as cystic fibrosis, diabetes, and acquired diseases such as cancer, as disclosed in U.S. patent application Ser. No. 08/143,312, the disclosure of which is incorporated herein. Genetic mutations may be detected by sequencing by hydridization. In one embodiment, genetic markers may be sequenced and mapped using Type-IIs restriction endonucleases as disclosed in U.S. Pat. No. 5,710,000, the disclosure of which is incorporated herein.
[0089] Other applications include chip based genotyping, species identification and phenotypic characterization, as described in U.S. patent application Ser. No. 08/797,812, filed Feb. 7, 1997, and U.S. application Ser. No. 08/629,031, filed Apr. 8, 1996, the disclosures of which are incorporated herein.
[0090] Gene expression may be monitored by hybridization of large numbers of mRNAs in parallel using high density arrays of nucleic acids in cells, such as in microorganisms such as yeast, as described in Lockhart et al, Nature Biotechnology,14:1675-1680 (1996), the disclosure of which is incorporated herein. Bacterial transcript imaging by hybridization of total RNA to nucleic acid arrays may be conducted as described in Saizieu et al., Nature Biotechnology,16:45-48 (1998), the disclosure of which is incorporated herein.
[0091] All publications cited herein are incorporated herein by reference in their entirety.
[0092] The invention will be further understood by the following non-limiting examples.
EXAMPLES
Example 1
[0093] Silicon compounds were obtained commercially or synthesized from commercially available starting materials. Silicon compounds N,N-bis(2-hydroxyethyl) -3-aminopropyltriethoxysilane, and N-(2-hydroxyethyl)-N-methyl-3-aminopropyltriethoxysilane (compound I) were purchased from Gelest, Inc (Tullytown, Pa).
[0094] Silicon compounds II and V and were prepared as shown in Schemes II and III. Solutions of the starting materials, bis(trimethoxysilyl-propyl)amine and bis[(3-trimethoxysilyl) propyl]ethylenediamine in methanol (62 wt %, from Gelest, Inc.) were combined with 1.1-2.2 theoretical equivalents of ethylene oxide at room temperature under a dry ice-acetone condenser. The resulting solutions were analyzed by 1H-NMR, which indicated 95% conversion to the hydroxyethylated products, and these were used without further purification.
[0095] 1H-NMR(CDCl3) data are provided below:
[0096] (II): 0.55-0.70 (br m, 4H), 1.55-1.65 (br m, 4H), 2.40-2.50 (br m, 2H), 2.55-2.60 (br m, 4H), 3.50 (s, MeOH), 3.55 (d, 9H), 3.75 (t, 2H);
[0097] (V): 0.55-0.70 (br m, 4H), 1.50-1.65 (br m, 4H), 2.40-2.80 (br m, 12H), 3.50 (s, MeOH), 3.40-3.60 (m-s, ˜20H), 3.75 (m, ˜3-4H);
[0098] Substrates were treated by a silanation procedure as follows. Glass substrates (borosilicate float glass, 2″×3″×0.027″, obtained from U.S. Precision Glass (Santa Rosa, Calif.) were cleaned by soaking successively in Nanostrip (Cyantek, Fremont, Calif.) for 15 minutes, 10% aqueous NaOH/70° C. for 3 minutes, and then 1% aqueous HCl for 1 minute (rinsing thoroughly with deionized water after each step). Substrates were then spin-dried for 5 minutes under a stream of nitrogen at 35° C. Silanation was carried out by soaking under gentle agitation in a freshly prepared 1-2% (wt/vol) solution of the silicon compound in 95:5 ethanol-water for 15 minutes. The substrates were rinsed thoroughly with 2-propanol, then deionized water, and fmally spin-dried for 5 minutes at 90°-110° C.
[0099] The stability of silicon compound bonded phase was evaluated. The surface hydroxyalkylsilane sites on the resulting substrates were “stained” with fluorescein in a checkerboard pattern by first coupling a MeNPOC-HEG linker phosphoramidite, image-wise photolysis of the surface, then coupling to the photo-deprotected linker sites a 1:20 mixture of fluorescein phosphoramidite and DMT-T phosphoramidite (Amersham-Pharmacia Biotech, Piscataway, N.J.), and then deprotecting the surface molecules in 1:1 ethylenediamine-ethanol for 4 hr. The steps were conducted using standard protocols, as described in Mcgall et al., J Am. Chem. Soc.,119: 5081-5090 (1997), the disclosure of which is incorporated herein.
[0100] The pattern and intensity of surface fluorescence was imaged with a scanning laser confocal fluorescence microscope, which employed excitation with a 488 nm argon ion laser beam focused to a 2 micron spot size at the substrate surface. Emitted light was collected through confocal optics with a 530(+15) nm bandpass filter and detected with a PMT equipped with photon counting electronics. Output intensity values (photon counts/second) are proportional to the amount of surface-bound fluorescein, so that relative yields of free hydroxyl groups within different regions of the substrate could be determined by direct comparison of the observed surface fluorescence intensities. All intensity values were corrected for nonspecific background fluorescence, taken as the surface fluorescence within the non-illurninated regions of the substrate.
[0101] The relative surface reactive site density was measured. For each silicon compound tested, the number of available surface synthesis sites achieved per unit area was estimated, relative to N,N-bis(2-hydroxyethyl)-3-aminopropyl-triethoxysilane, by comparison of the observed initial surface fluorescence intensities of the various substrates immediately after deprotection in ethanolic diaminoethane.
[0102] To determine the relative stability of the silicon compound coatings, substrates were gently agitated on a rotary shaker at 45° C. in 5×SSPE aqueous buffer (BioWhittacker Products, Walkersville, Md.) at pH 7.3. Periodically, the substrates were removed from the buffer and re-scanned to measure the amount of fluorescein remaining bound to the surface.
[0103] The results are shown in FIG. 11. As shown in FIG. 11, more of the fluorescein tag remained bound to the substrate after prolonged exposure to the aqueous buffer in the case of substrates silanated with II or V, than remained bound to the substrates silanated with N,N-bis(2-hydroxyethyl)-3-aminopropyltriethoxysilane or compound I. This demonstrates that the surface bonded phase obtained with silicon compounds II or V is much more stable towards hydrolysis than that obtained with N,N-bis(2-hydroxyethyl)-3-aminopropyl-triethoxysilane.
[0104] The hybridization performance of silanated substrates was evaluated. A comparison was made between substrates silanated with N,N-bis(2-hydroxyethyl)-3-aminopropyltriethoxysilane and compound V in terms of performance under typical hybridization assay conditions. A nucleic acid probe sequence (5′-GTC AAG ATG CTA CCG TTC AG-3′) (SEQ. ID NO. 1) was synthesized photolithographically in a checkerboard array pattern (400×400 micron features) on the substrates that had been derivatized with either NN-bis(2-hydroxyethyl)-3-aminopropyltriethoxysilane or silicon compound V. After deprotection in ethanolic diaminoethane, the arrays were hybridized with a fluorescein-labeled complementary “target” nucleic acid (5′-fluorescein-CTG AAC GGT AGC ATC TTG AC-3′) (SEQ. ID NO. 2) at a concentration of 250 pM in 6×SSPE buffer (0.9 M NaCl, 60 mM NaH2PO4, 6 mM EDTA, pH 7.5) for 16 hours at 45° C. After cooling to room temperature, the target nucleic acid solution was removed, and the array was washed briefly with 6× SSPE buffer and then scanned on a confocal imaging system. The relative amount of bound target was determined from the fluorescence signal intensity. The hybridization signal intensities obtained with the more stable substrates, derivatized with silicon compound V, were at least four times higher than those obtained with substrates that were derivatized with N,N-bis(2-hydroxyethyl)-3-aminopropyltriethoxysilane. A graph of fluorescence signal intensity vs. silane is shown in FIG. 12.
Claims
Post-issuance certificates present
The text shown below may not reflect later post-issuance changes.
What is claimed is:
1. A functionalized silicon compound having a structure of Formula 2:
wherein R1and R2are independently selected from the group consisting of alkoxy and halide, and R3is selected from the group consisting of alkoxy, halide and alkyl;
wherein L1and L2are both —(CH2)n—, wherein n=2 to 10; and
wherein A1is a moiety comprising one or more derivatizable functional groups selected from the group consisting of hydroxyl, amino, carboxyl, thio, halo and sulfonate.
2. The functionalized silicon compound of claim 1, wherein A1comprises a plurality of the derivatizable functional groups.
3. A functionalized silicon compound having a structure of Formula 2:
wherein R1and R2are independently selected from the group consisting of alkoxy and halide, and R3is selected from the group consisting of alkoxy, halide and alkyl;
wherein L1and L2are both —(CH2)n—, wherein n=2 to 10; and
wherein A1is a moiety comprising a hydroxyl group.
4. The functionalized silicon compound of claim 1, wherein the silicon compound is compound II:
5. A method of fimctionalizing a surface, the method comprising covalently attaching to the surface a functionalized silicon compound, wherein the functionalized silicon compound comprises at least one derivatizable functional group and a plurality of activated silicon groups, wherein the silicon compound is a compound having a structure of Formula 2:
wherein R1and R2are independently selected from the group consisting of alkoxy and halide, and R3is selected from the group consisting of alkoxy, halide and alkyl;
wherein L1and L2are both —(CH2)n—, wherein n=2 to 10; and
wherein A1is a moiety comprising one or more derivatizable functional groups selected from the group consisting of hydroxyl, amino, carboxyl, thio, halo and sulfonate.
6. The method of claim 5, wherein the derivatizable functional group is a hydroxyl group.
7. The method of claim 5, wherein A1comprises a plurality of the derivatizable functional groups.
8. The method of claim 5, wherein the silicon compound is compound II:
9. The method of claim 5, wherein the surface is the surface of a substrate comprising silica.
10. The method of claim 5, wherein the substrate is in a form selected from the group consisting of particles, films and chips.
11. The method of claim 5, wherein the method comprises covalently attaching a plurality of functionalized silicon compounds surface; and
forming an array of nucleic acids covalently attached to the functionalized silicon compounds on the surface.
12. The method of claim 11, wherein the derivatizable functional group is hydroxyl.
13. The method of claim 6, wherein the hydroxyl group is activated or protected.
14. The method of claim 12, wherein the hydroxyl group is activated or protected.
15. The compound of claim 3, wherein the hydroxyl group is activated or protected.
16. The method of claim 12, wherein the density of the covalently attached nucleic acids on the surface is greater than about 60 different nucleic acids per 1 cm2.
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