Method for attachment of silylated molecules to glass surfaces

a silylated molecule and glass surface technology, applied in the field of microarray biomolecule detection technology, can solve the problems of inability to give reproducible silane, and inability to achieve reproducible optimum surface loading, so as to enhance the detection of target analytes

Inactive Publication Date: 2007-06-14
NANOSPHERE INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0005] The present invention fulfills the need in the art for methods for the attachment of molecules such as oligonucleotides onto unmodified surfaces such as a glass surface without the need for laborious synthetic steps, with increase surface loading densities, and with greater reproducibility and which avoids the need for pre-surface modifications. Molecules such as DNA can be silylated at either the 3′ or 5′ ends as discussed below and the 3′ or 5′-silylated DNA may then be covalently attached directly to a surface such as a pre-cleaned glass surface (Scheme) for use in hybridization assays. Furthermore, thorough the use of certain silylating reagents, it is now possible to further enhance surface loading densities by using modified silylating agents having multiple molecules attached thereto. The present invention thus provides novel methods for attaching molecules onto a substrate, devices prepared by such methods, and compositions. This method provides great advantages over the present technology in terms of simplicity, cost, speed, safety, and reproducibility.
[0013] (c) contacting the second reactive intermediate with said surface so as to immobilized the molecule onto said surface. The method allows for the production of branched captured molecules structures such as branched oligonucleotides on a surface which is useful for enhancing detection of target analytes such as nucleic acids.

Problems solved by technology

After coating the surface with reactive silanes, the next challenge is immobilization of required biomolecules on the modified surface.
The surface loadings always vary with different silanes and even same silane may not give reproducible results.
Reproducibility of optimum surface loading has always been a great challenge in this field since surface loading dictates the performance of the assay.
Even with simple linear molecules for immobilization, the optimum loading on the surface is difficult to achieve.
All these reported methods involve silylating step which uses expensive reagents and analytical tools.
Also, these methods are also multi-step processes that are labor intensive and expensive8-9.
Earlier reported methods have involved a laborious synthesis and time consuming procedure7.
Indeed, many of the current immobilization methods suffer from one or more of a number of disadvantages.
Some of these are, complex and expensive reaction schemes with low oligonucleotide loading yields, reactive unstable intermediates prone to side reactions and unfavorable hybridization kinetics of the immobilized oligonucleotide.

Method used

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  • Method for attachment of silylated molecules to glass surfaces
  • Method for attachment of silylated molecules to glass surfaces
  • Method for attachment of silylated molecules to glass surfaces

Examples

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example 1

Preparation of DNA Array Chips

[0058] This Example provides a general procedure for the covalent attachment of a molecule, e.g., 3′ or 5′-silylated DNA, directly to surfaces such as pre-cleaned glass surface via single silylated molecule or dendritic silylated molecule procedure.

(a) Method No. 1

[0059] As shown in FIG. 1, a method is shown for attaching a 3′-amino or 5′-amino DNA molecule to a pre-cleaned glass surface. 3′-Amine linked DNA is synthesized by following standard protocol for DNA synthesis on DNA synthesizer. The 3′ amine modified DNA synthesized on the solid support was attached through succinyl linker to the solid support. After synthesis, DNA attached to the solid support was released by using aqueous ammonia, resulting in the generation of a DNA strand containing a free amine at the 3′-end. The crude material was purified on HPLC, using triethyl ammonium acetate (TEAA) buffer and acetonitrile. The dimethoxytrityl (DMT) group was removed on the column itself using ...

example 2

Detection of Factor V Target Sequence Using a DNA Array Chip

[0063] This Example illustrates that DNA plates prepared as described in Example 1 are useful for sandwich hybridization assays for detection of nucleic acid targets.

(a) Gold Colloid Preparation:

[0064] Gold colloids (13 nm diameter) were prepared by reduction of HAuCl4 with citrate as described in Frens, Nature Phys. Sci., 241, 20 (1973) and Grabar, Anal. Chem., 67, 735 (1995). Briefly, all glassware was cleaned in aqua regia (3 parts HCl, 1 part HNO3), rinsed with Nanopure H2O, then oven dried prior to use. HAuCl4 and sodium citrate were purchased from Aldrich Chemical Company. Aqueous HAuCl4 (1 mM, 500 mL) was brought to reflux while stirring. Then, 38.8 mM sodium citrate (50 mL) was added quickly. The solution color changed from pale yellow to burgundy, and refluxing was continued for 15 min. After cooling to room temperature, the red solution was filtered through a Micron Separations Inc. 1 micron filter. Au colloid...

example 3

Detection of M13 Target Sequence Using DNA Array Chip

[0078] In this Example, probe was targeted directly to the capture strand and a detection assay was performed. Plates Nos. 1-3 were prepared as described in Example 1 (method no. 1). In Plates 2 & 3, probes (FIG. 6) were clearly hybridized to the capture strand within 45 minutes. The gold colloid nanoparticles hybridized to the capture were clearly visible before silver amplification. In plate no 1 (FIG. 6), a different probe was used and the assay was developed to show the specificity. After silver stain development, signals were not shown on the glass surface even after silver amplification. This experiment established the specificity of the DNA chip prepared in accordance with the invention.

[0079] M13 Capture sequence:

(SEQ ID NO: 8)5′-tga aat tgt tat c-NH-CO-NH--Si-(OEt)3-3′

[0080] Probe used on plates Nos. 2-3 plates:

3′-act tta aca ata g-a20-Epi-5′(SEQ ID NO: 9)

[0081] On plate no.1, a detection probe 3′-t taa cac tcg c-a2...

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Abstract

A method for the efficient immobilization of silylated molecules such as silylated oligonucleotides or proteins onto unmodified surfaces such as a glass surface is provided. Also provided are compounds, devices, and kits for modifying surfaces such as glass surfaces.

Description

CROSS-REFERENCE [0001] This application claims the benefit of U.S. Provisional application No. 60 / 383,564, filed May 28, 2003, which is incorporated by reference in its entirety.BACKGROUND OF THE INVENTION [0002] Surface modification plays an important role in micro-array biomolecule detection technology for controlling backgrounds and spot morphology. Several modifications were developed using different type of commercially available silanes such as silyl amines, aldehydes, thiols etc. for immobilization of biomolecules such as oligonucleotides. After coating the surface with reactive silanes, the next challenge is immobilization of required biomolecules on the modified surface. The surface loadings always vary with different silanes and even same silane may not give reproducible results. Reproducibility of optimum surface loading has always been a great challenge in this field since surface loading dictates the performance of the assay. Even with simple linear molecules for immobi...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C12Q1/68C12M1/34B05D3/00C03C17/30G01N33/552
CPCC03C17/30C12Q1/6834Y10T436/20Y10T436/17Y10T436/172307G01N33/552
Inventor GARIMELLA, VISWANADHAMBERNAL, YASMITH
Owner NANOSPHERE INC
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