Three-dimensional probe carriers

• US 20020055111A1
• Filed: 08/24/2001
• Published: 05/09/2002
• Est. Priority Date: 08/25/2000
• Status: Abandoned Application

• Current Assignee: Genespectra, Inc.
• Original Assignee: Genespectra, Inc.
• Inventors: Luo, Yuling, Chen, Anthony, Chen, Shiping
• Application Number:
  US09/938,798
• Publication Number:
  US 20020055111A1
• Time in Patent Office: Days
• US Class Current: 435/6
• 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 2219/00315 Microtiter plates
• CPC Class Codes: B01J 2219/00317 Microwell devices, i.e. having large numbers of wells
• CPC Class Codes: B01J 2219/00351 Means for dispensing and evacuation of reagents
• CPC Class Codes: B01J 2219/00509 Microcolumns
• CPC Class Codes: B01J 2219/00522 in a multiple parallel arrangement
• CPC Class Codes: B01J 2219/00524 in the shape of fiber bundles
• CPC Class Codes: B01J 2219/00585 Parallel processes
• CPC Class Codes: B01J 2219/00596 Solid-phase processes
• CPC Class Codes: B01J 2219/00605 the compounds being directly bound or immobilised to solid supports
• CPC Class Codes: B01J 2219/00608 DNA chips
• CPC Class Codes: B01J 2219/0061 The surface being organic
• CPC Class Codes: B01J 2219/00612 the surface being inorganic
• CPC Class Codes: B01J 2219/00619 using hydrophilic or hydrophobic regions
• CPC Class Codes: B01J 2219/00621 by physical means, e.g. trenches, raised areas
• CPC Class Codes: B01J 2219/00641 the porous medium being continuous, e.g. porous oxide substrates
• CPC Class Codes: B01J 2219/00659 Two-dimensional arrays
• CPC Class Codes: B01J 2219/00664 Three-dimensional arrays
• CPC Class Codes: B01J 2219/00673 Slice arrays
• CPC Class Codes: B01J 2219/00675 In-situ synthesis on the substrate
• CPC Class Codes: B01J 2219/00677 : Ex-situ synthesis followed by deposition on the substrate
• CPC Class Codes: B01J 2219/00704 : integrated with the reactor apparatus
• CPC Class Codes: B01J 2219/0072 : Organic compounds
• CPC Class Codes: B01L 2400/0475 : specific mechanical means and fluid pressure
• CPC Class Codes: B01L 2400/0487 : fluid pressure, pneumatics
• CPC Class Codes: B01L 3/5025 : for parallel transport of multiple samples
• CPC Class Codes: B01L 3/5085 : for multiple samples, e.g. microtitration plates
• CPC Class Codes: B82Y 30/00 : Nanotechnology for materials or surface science, e.g. nanocomposites
• CPC Class Codes: C03B 2201/20 : doped with non-metals other than boron or fluorine
• CPC Class Codes: C03B 2201/31 : doped with germanium
• CPC Class Codes: C03B 2203/16 : Hollow core
• CPC Class Codes: C03B 37/01413 : Reactant delivery systems C03B37/01807 takes precedence; devices therefor in general B01D1/00, B01J4/00
• CPC Class Codes: C03B 37/01807 : Reactant delivery systems, e.g. reactant deposition burners
• CPC Class Codes: C03B 37/0756 : Hollow fibres
• CPC Class Codes: C40B 50/14 : Solid phase synthesis, i.e. wherein one or more library building blocks are bound to a solid support during library creation; Particular methods of cleavage from the solid support
• CPC Class Codes: G01N 2021/6484 : Optical fibres
• CPC Class Codes: G01N 2021/7786 : Fluorescence
• CPC Class Codes: G01N 21/645 : Specially adapted constructive features of fluorimeters
• CPC Class Codes: G01N 21/648 : using evanescent coupling or surface plasmon coupling for the excitation of fluorescence
• CPC Class Codes: G01N 21/7703 : using reagent-clad optical fibres or optical waveguides using measurement of total internal reflection or attenuated total reflection G01N21/552; optical fibres or waveguides per se G02B
• CPC Class Codes: G02B 6/06 : the relative position of the fibres being the same at both ends, e.g. for transporting images

Abstract

The inventions disclosed herein provide a novel 3-dimensional arrangement of probes on a probe carrier with concomitant increases in the economy of reagents, compactness and readability of the probe carriers. Novel methods of fabricating probe carriers are also disclosed. Techniques for hybridization assays and reading results of such assays are also presented.

Claims

1. A three dimensional probe array comprising a substrate formed of a substrate material and having multiple probe wells, each of said probe wells having a top surface, a bottom surface, an inner sidewall, an opening in said top surface, and an opening in said bottom surface;

wherein a first probe well of said multiple probe wells contains probes, wherein the first probe well comprises a first light-conducting material and a second material, and wherein said first light-conducting material and said second material are configured such that a light beam launched into the opening of the first probe well in said top surface is transmitted by said first light-conducting material and exits the opening of said first probe well in said bottom surface.

2. A three dimensional probe array according to claim 1 wherein said first light-conducting material has a first refractive index and said second material has a second refractive index that is less than the first refractive index such that the first probe well forms a light-conducting waveguide.

3. A three dimensional probe array according to claim 2 wherein the first light-conducting material of the first probe well comprises a liquid in fluid contact with the inner sidewall of the first probe well and the second material comprises said sidewall.

4. A three dimensional probe array according to claim 2 wherein the first light-conducting material comprises a first portion of the first probe well that includes the inner sidewall and the second material comprises a portion of the substrate.

5. A three dimensional probe array according to claim 2 wherein the first light-conducting material comprises a first portion of the first probe well that includes the inner sidewall and the second material comprises a second portion of the first probe well bounded by said first portion and an outer sidewall of the first probe well.

6. A three dimensional probe array according to claim 2 wherein said first light-conducting material comprises silica doped with an impurity that increases the refractive index of silica and wherein the second portion comprises silica having a lower refractive index than said first portion.

7. A three dimensional probe array according to claim 2 wherein the first light-conducting material comprises a reflective material.

8. A three dimensional probe array according to claim 7 wherein the reflective material comprises multiple dielectric thin films deposited on the inner sidewall of the first probe well.

9. A three dimensional probe array according to claim 7 wherein the reflective material comprises metal deposited on the inner sidewall of the first probe well.

10. A three dimensional probe array according to claim 1 wherein the first probe well comprises a capillary.

11. A three dimensional probe array according to claim 1 wherein the substrate comprises multiple tubes having a length and adhered to one another along the length and along outer sidewalls of the tubes.

12. A three dimensional probe array according to claim 1 wherein each of said multiple probe wells individually comprises a capillary.

13. A three dimensional probe array according to claim 12 wherein each of said multiple probe wells forms a portion of a unitary array of said probe wells.

14. A three dimensional probe array according to claim 12 wherein each of said multiple probe wells forms a portion of a bundle of said probe wells.

15. A three dimensional probe array according to claim 1 wherein the multiple probe wells comprise multiple capillaries bound together to form a bundle.

16. A three dimensional probe array according to claim 15 wherein said bundle is an unordered bundle.

17. A three dimensional probe array according to claim 15 wherein said bundle is an ordered bundle.

18. A three dimensional probe array according to claim 16 wherein the substrate comprises a binder that holds the capillaries together.

19. A three dimensional probe array according to claim 18 wherein the binder comprises at least one member of the group consisting of epoxy, silica, a metal band, a plate having through-holes through which the capillaries pass, and a plate to which each of the bottom surfaces of the probe wells is attached.

20. A three dimensional probe array according to claim 1 wherein the opening in the top surface and the opening in the bottom surface of the first probe well form a portion of a channel through the first probe well, which channel has a length and which channel has a cross-sectional area that is essentially constant along the length of the channel.

21. A three dimensional probe array according to claim 1 wherein the opening in the top surface and the opening in the bottom surface of the first probe well form a portion of a channel through the first probe well, which channel has a length and which channel has a cross-sectional area that decreases along the length of the channel.

22. A three dimensional probe array according to claim 1 wherein the probe array further comprises a base plate to which the bottom surface of the first probe well is attached.

23. A three dimensional probe array according to claim 1 wherein said probe wells are distributed across the substrate at a density greater than 400 probe wells per square centimeter.

24. A three dimensional probe array according to claim 1 wherein the probes comprise at least one member selected from the group consisting of biological and chemical samples.

25. A three dimensional probe array according to claim 1 wherein the probes are attached to the inner sidewalls of the probe wells.

26. A three dimensional probe array according to claim 1 wherein the probes are suspended in a liquid contained in said probe wells.

27. A three dimensional probe array according to claim 1 wherein the probe wells comprise silica.

29. An array of pillars according to claim 28, wherein said surface of said substrate is planar.

30. An array of pillars according to claim 28, wherein said substrate is a rod having two ends and a sidewall, wherein said surface of the substrate comprises said sidewall.

31. An array of pillars according to claim 28, wherein said distal end of each said pillar is free of biological and chemical sample.

32. An array of pillars according to claim 28, wherein the longest axis of each said pillar is less than 200 μ

m.

33. An array of pillars according to claim 28, wherein said pillars are distributed across said substrate at a density greater than 400 pillars per square centimeter of substrate surface.

34. An array of pillars according to claim 28, wherein said pillars each have an electrically conductive core.

35. An array of pillars according to claim 28, wherein said pillars are light-conducting pillars.

38. A method of generating an array of capillaries according to claim 37, wherein said capillaries are light conducting capillaries.

39. A method of generating an array of capillaries according to claim 38, further comprising registering the proximal ends of the capillaries to the distal ends of the capillaries.

40. A method of generating an array of capillaries according to claim 39, wherein said registering comprises launching light into a distal end of a first capillary, observing the light exiting a proximal end of the first capillary and recording information that correlates the distal end of the first capillary to the proximal end of the first capillary.

41. A method of generating an array of capillaries according to claim 40, wherein said biological or chemical samples bind to the sidewall of said channels of said capillaries.

42. A method of generating an array of capillaries according to claim 41, wherein said channel of each said capillary is coated with a material such that the coating reflects light within the channel.

43. A method of generating an array of capillaries according to claim 36, wherein said capillaries further comprise a first portion having a first refractive index and a second potion having a second refractive index, said second refractive index being greater than said first refractive index, wherein said first and second portion are configure such that a beam of light launched into the proximal end is transmitted along the capillary and exits the capillary at the distal end.

44. A method of generating an array of capillaries according to claim 37, wherein said capillaries further comprise a first portion having a first refractive index and a second potion having a second refractive index, said second refractive index being greater than said first refractive index, wherein said first and second portion are configure such that a beam of light launched into the proximal end is transmitted along the capillary and exits the capillary at the distal end.

45. A method of binding a target to probes in a probe array comprising:

a) providing a probe array according to claim 1;

and

b) pumping a fluid containing target molecules from a first fluid reservoir through at least one probe well to a second fluid reservoir.

46. A method of binding a target to probes in capillary arrays according to claim 45, further comprising pumping said fluid from the second fluid reservoir through said probe well through which said fluid was previously pumped.

47. A method of detecting target molecules bound to probe molecules in a probe array comprising:

a) providing a probe array according to claim 1;

b) transmitting a light into a first portion of a first capillary; and

c) detecting whether target molecules are bound to the biological or chemical sample within said first capillary based upon an observable effect caused by transmitting said light into said capillary.

49. A method according to claim 48 wherein said bundle is a random bundle of pillars.

50. A method according to claim 48 wherein said bundle of pillars is formed by threading a plurality of said pillars through at least one guide plate.

51. A method of manufacturing an array of pillars according to claim 48, further comprising affixing each said slice to a substrate such that the proximal ends of said pillars are affixed to said substrate.

52. A method of manufacturing an array of pillars according to claim 48, wherein each said pillar comprises a material capable of transmitting a signal from the distal end to the proximal end.

53. A method of manufacturing an array of pillars according to claim 52, further comprising registering said proximal ends of the pillars to the distal ends of the pillars.

54. A method of manufacturing an array of pillars according to claim 53, wherein the act of registering the proximal ends to the distal ends comprises launching a signal into a distal end of a first pillar, observing the signal at a proximal end of the first pillar, and recording information that correlates the distal end of the first pillar to the proximal end of the first pillar.

55. A method of manufacturing an array of pillars according to claim 54, wherein said signal is light.

56. A method of manufacturing an array of pillars according to claim 54, wherein said signal is electrical.

58. A method according to claim 57, wherein said pillars further comprise an electrically conductive core and wherein efficiency of binding is enhanced by applying to said pillar core a voltage of opposite polarity to the overall charge of the target molecules.

59. A method according to claim 57, wherein said pillars further comprise an electrically conductive core and wherein efficiency of binding is enhanced by applying an alternating voltage to said pillar cores.

60. A method of binding a probe to target molecules adhered to an array of pillars according to claim 57, wherein said pillars further comprise an electrically conductive core and further comprising enhancing binding specificity by applying to said pillar cores a voltage of the same polarity as the overall charge of the non-target molecules.

28. An array of pillars comprising multiple pillars having proximal ends, distal ends, and sidewalls, wherein said proximal ends of said pillars are affixed to a surface of a substrate, and each of said pillars has a probe attached to the sidewalls of said pillars.

57. A method of binding a probe to target molecules adhered to an array of pillars comprising:

a) providing an array of pillars according to claim 28; and

b) contacting the sidewalls of said pillars with a target-containing fluid.

36. A method of generating an array of capillaries comprising:

a) forming an ordered bundle of a plurality of light conducting capillaries having distal and proximal ends and a channel extending from said distal end to said proximal end, wherein each said capillary is capable of conducting light parallel to the channel, and wherein the position of the distal end and proximal end of each said capillary are known;

b) securing the proximal ends of the capillaries to form a solid mass containing the proximal ends of said capillaries, said solid mass having a facet and said proximal ends being substantially coplanar at said facet; and

c) cutting said bundle into slices, wherein said capillaries are filled with biological or chemical samples prior to cutting into said slices.

37. A method of generating an array of capillaries comprising:

a) forming a random bundle of a plurality of capillaries having distal and proximal ends;

b) securing the proximal ends of the capillaries to form a solid mass containing the proximal ends of said capillaries, said solid mass having a facet and said proximal ends being substantially coplanar at said facet; and

c) cutting said bundle into slices, wherein said capillaries are filled with biological or chemical samples prior to cutting into slices.

48. A method of manufacturing an array of pillars comprising:

a) attaching biological or chemical samples to a sidewall of a plurality of pillars having proximal and distal ends;

b) coating said pillars with a removable protective layer;

c) forming a bundle of said pillars;

d) securing the proximal ends of said pillars to form a solid mass containing the proximal ends of the pillars, said solid mass having a facet and said proximal ends being substantially coplanar at said facet; and

e) cutting said bundle into slices.

61. A method of detecting binding of a probe to target molecules adhered to an array of pillars comprising:

a) providing an array of pillars comprising a plurality of pillars having proximal and distal ends, wherein said proximal ends are affixed to a substrate, and each of said pillars has a biological or chemical sample attached to the sidewalls of said pillar;

b) contacting the sidewalls of said pillars to a target molecule-containing fluid; and

c) detecting said target molecules bound to said chemical or biological samples.

62. A method of detecting binding of a probe to target molecules adhered to an array of pillars according to claim 61, wherein said pillars are light conducting pillars and wherein said detecting is performed by transmitting a light signal into a first pillar.

63. A method of detecting binding of a probe to target molecules adhered to an array of pillars according to claim 62, wherein said light signal induces target molecules bound to said first pillar to emit a second light signal.