Microfabricated, flowthrough porous apparatus for discrete detection of binding reactions

• US 5,843,767 A
• Filed: 04/10/1996
• Issued: 12/01/1998
• Est. Priority Date: 10/28/1993
• Status: Expired due to Term

• Current Assignee: UT-Battelle LLC
• Original Assignee: Houston Advanced Research Center
• Inventors: Beattie, Kenneth L.
• Primary Examiner(s): Hutzell, Paula K.
• Assistant Examiner(s): BAKALYAR, HEATHER
• Application Number:
  US08/631,751
• Time in Patent Office: 965 Days
• Field of Search: 435/6, 435/970, 435/973, 435/287.1, 435/287.2, 436/518, 436/524, 436/525, 436/527, 436/805, 436/807, 436/808, 422/68.1, 422/82.05, 536/24.3, 536/24.31, 536/24.32, 427/243, 428/426, 428/429
• US Class Current: 435/287.1
• CPC Class Codes: B01J 19/0046 Sequential or parallel reactions, e.g. for the synthesis of polypeptides or polynucleotides; Apparatus and devices for combinatorial chemistry or for making molecular arrays synthesis methods per se C40B50/00
• CPC Class Codes: B01J 19/0093 Microreactors, e.g. miniaturised or microfabricated reactors laboratory containers with capillary fluid transport in microfabricated channels or chambers B01L3/5027
• CPC Class Codes: B01J 2219/00317 Microwell devices, i.e. having large numbers of wells
• CPC Class Codes: B01J 2219/00319 the blocks being mounted in stacked arrangements
• CPC Class Codes: B01J 2219/00351 Means for dispensing and evacuation of reagents
• CPC Class Codes: B01J 2219/00416 Vacuum
• CPC Class Codes: B01J 2219/00585 Parallel processes
• CPC Class Codes: B01J 2219/00659 Two-dimensional arrays
• CPC Class Codes: B01J 2219/00722 Nucleotides
• CPC Class Codes: B01J 2219/00725 Peptides
• CPC Class Codes: B01J 2219/00828 Silicon wafers or plates
• CPC Class Codes: B01J 2219/00831 Glass
• CPC Class Codes: B01J 2219/00844 Comprising porous material
• CPC Class Codes: B01L 3/5025 for parallel transport of multiple samples
• CPC Class Codes: B01L 3/50255 Multi-well filtration
• CPC Class Codes: C12Q 1/6874 involving nucleic acid arrays, e.g. sequencing by hybridisation
• CPC Class Codes: C40B 40/06 Libraries containing nucleotides or polynucleotides, or derivatives thereof
• CPC Class Codes: C40B 40/10 Libraries containing peptides or polypeptides, or derivatives thereof
• CPC Class Codes: C40B 60/14 for creating libraries
• CPC Class Codes: Y10S 435/97 Test strip or test slide
• CPC Class Codes: Y10S 435/973 : Simultaneous determination of more than one analyte
• CPC Class Codes: Y10S 436/805 : Optical property
• CPC Class Codes: Y10S 436/807 : Apparatus included in process claim, e.g. physical support structures
• CPC Class Codes: Y10S 436/808 : Automated or kit
• CPC Class Codes: Y10T 428/31612 : As silicone, silane or siloxane

Abstract

An improved microfabricated apparatus for conducting a multiplicity of individual and simultaneous binding reactions is described. The apparatus comprises a substrate on which are located discrete and isolated sites for binding reactions. The apparatus is characterized by discrete and isolated regions that extend through said substrate and terminate on a second surface thereof such that when a test sample is allowed to the substrate, it is capable of penetrating through each such region during the course of said binding reaction. The apparatus is especially useful for sequencing by hybridization of DNA molecules.

Claims

1. A device for binding a target molecule, comprising:

a substrate having oppositely facing first and second major surfaces;

a multiplicity of discrete channels extending through said substrate from said first major surface to said second major surface;

a first binding reagent immobilized on the walls of a first group of said channels, and

a second binding reagent immobilized on the walls of a second group of said channels.

2. A device according to claim 1, wherein said first and second binding reagents differ from one another.

3. A device according to claim 1, wherein said first and second binding reagents bind different target molecules.

4. A device according to claim 2, comprising discrete channels having diameters of from about 0.033 micrometers to about 10 micrometers.

5. A device according to claim 2, comprising discrete channels having cross sectional areas of between about 8.5×

10^-4 μ

m² to 80 μ

m².

6. A device according to claim 2, comprising a substrate between about 100 μ

m to about 1000 μ

m thick.

7. A device according to claim 2, comprising channels having an inner surface area of between about 10 μ

m² and about 3×

10⁴ μ

m².

8. A device according to claim 2, wherein said groups of channels have areas of between about 20 μ

m² to about 3×

10⁶ μ

m².

9. A device according to claim 2, wherein there are between 400 and 4400 of said groups of discrete channels per cm² of cross-sectional area of the substrate.

10. A device according to claim 2, wherein the inner surface area of the channels in a group of channels is from about 100 to about 1000 times the cross sectional area of the group of channels.

11. A device according to claims 1, 2, 5, 7, 9, or 10, wherein said substrate is fabricated from glass or silicon.

12. A device according to claim 11, comprising a substrate made of nanochannel glass.

13. A device according to claim 11, comprising a substrate made of oriented array microporous silicon.

14. A device according to claims 1, 2, 5, 7, 9, or 10, wherein said binding reagents are effective for carrying out binding reactions selected from the group consisting of binding reactions involving small molecules, macromolecules, particles and cellular systems.

15. A device according to claim 14, wherein said binding reagents are effective for carrying out an analytical task selected from the group consisting of sequence analysis by hybridization, analysis of patterns of gene expression by hybridization of mRNA or cDNA to gene-specific probes, immunochemical analysis of protein mixtures, epitope mapping, assay of receptor-ligand interactions and profiling of cellular populations involving binding of cell surface molecules to specific ligands or receptors.

16. A device according to claim 15, wherein said binding reagents are selected from the group consisting of DNA, proteins and ligands.

17. A device according to claim 16, wherein said binding reagents are oligonucleotide probes.

18. A device according to claim 17, wherein the oligonucleotide probes are attached to channel surfaces via a primary amine group incorporated into the probes prior to immobilization.

19. A device according to claim 18, wherein said probes are attached to said channel surfaces via a terminal primary amine derivative of said polynucleotide and said glass substrate is derivatized with epoxysilane.

38. A device according to claims 1 or 20, comprising discrete channels having diameters of from about 0.45 micrometers to about 10 micrometers.

20. A device for binding a target molecule, comprising:

a substrate having oppositely facing first and second major surfaces;

a multiplicity of discrete channels extending through said substrate from said first major surface to said second major surface;

a first binding reagent immobilized on the walls of a first group of said channels, and

a second binding reagent immobilized on the walls of a second group of said channels,

further comprising a rigid support, wherein said rigid support is integral to said substrate, or is bonded to said substrate.

21. A device according to claim 20 wherein said support is integral to said substrate.

22. A device according to claim 20, wherein said support is bonded to said substrate.

23. A device according to claim 20, wherein said rigid support comprises wells for delivering fluids to subsets of channels of said substrate.

24. A device according to claim 20, comprising discrete channels having cross sectional areas of between about 8.5×

10^-4 μ

m² to about 80 μ

m².

25. A device according to claim 20, comprising channels having an inner surface area of between about 10 μ

m² and about 3×

10⁴ μ

m².

26. A device according to claim 20, wherein said groups of channels have areas of between about 20 μ

m² to about 3×

10⁶ μ

m².

27. A device according to claim 20, wherein there are between 400 and 4400 of said discrete channels per cm² of cross-sectional area of the substrate.

28. A device according to claim 20, wherein the inner surface area of the channels in a group of channels is from about 100 to about 1000 times the cross sectional area of the group of channels.

29. A device according to claims 20, 25, 28, comprising a substrate fabricated from glass or silicon.

30. A device according to claim 29, comprising a substrate made of nanochannel glass.

31. A device according to claim 29, comprising a substrate made of oriented array microporous silicon.

32. A device according to claims 20, 25, 28, wherein said binding reagents are effective for carrying out binding reactions selected from the group consisting of binding reactions involving small molecules, macromolecules, particles and cellular systems.

33. A device according to claim 32, wherein said binding reagents are effective for carrying out an analytical task selected from the group consisting of sequence analysis by hybridization, analysis of patterns of gene expression by hybridization of mRNA or CDNA to gene-specific probes, immunochemical analysis of protein mixtures, epitope mapping, assay of receptor-ligand interactions and profiling of cellular populations involving binding of cell surface molecules to specific ligands or receptors.

34. A device according to claim 33, wherein said binding reagents are selected from the group consisting of DNA, proteins and ligands.

35. A device according to claim 34, wherein said binding reagents are oligonucleotide probes.

36. A device according to claim 35, wherein the oligonucleotide probes are attached to channel surfaces via a primary amine group incorporated into the probes prior to immobilization.

37. A device according to claim 36, wherein said probes are attached to said channel surfaces via a terminal primary amine derivative of said polynucleotide and said glass substrate is derivatized with epoxysilane.