Substrates, systems and methods for analyzing materials

• US 8,053,742 B2
• Filed: 10/01/2010
• Issued: 11/08/2011
• Est. Priority Date: 09/01/2006
• Status: Active Grant

• Current Assignee: Pacific Bioscience of California Incorporated (L'Oreal SA)
• Original Assignee: Pacific Bioscience of California Incorporated (L'Oreal SA)
• Inventors: Turner, Stephen, Lundquist, Paul
• Primary Examiner(s): Kim; Kiho
• Application Number:
  US12/896,515
• Publication Number:
  US 20110082051A1
• Time in Patent Office: 403 Days
• Field of Search: 250/458.1
• US Class Current: 250/458.1
• CPC Class Codes: G01N 2021/7786 Fluorescence
• CPC Class Codes: G01N 21/6428 Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" in vivo A61B5/00; immunoassay G01N33/53
• CPC Class Codes: G01N 21/6452 Individual samples arranged in a regular 2D-array, e.g. multiwell plates
• 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 6/43 Arrangements comprising a plurality of opto-electronic elements and associated optical interconnections

Abstract

Substrates, systems and methods for analyzing materials that include waveguide arrays disposed upon or within the substrate such that evanescent fields emanating from the waveguides illuminate materials disposed upon or proximal to the surface of the substrate, permitting analysis of such materials. The substrates, systems and methods are used in a variety of analytical operations, including, inter alia, nucleic acid analysis, including hybridization and sequencing analyses, cellular analyses and other molecular analyses.

Claims

1. An analytical device, comprising:

a substrate comprising a first surface and an array of optical waveguide cores proximal to the first surface;

a plurality of optically resolvable molecular complexes, each of which is immobilized sufficiently proximal to the first surface to be illuminated by an evanescent field emanating from at least one of the optical waveguide cores when light is passed through said array; and

at least a first excitation radiation source optically coupled to the array to provide the evanescent field by passing excitation light into the array.

2. The device of claim 1, wherein at least a portion of each of the optical waveguide cores is disposed beneath the first surface of the substrate.

3. The device of claim 2, wherein each of the optical waveguide cores is exposed at the first surface of the substrate.

4. The device of claim 2, wherein each of the optical waveguide cores is imbedded beneath the first surface of the substrate.

5. The device of claim 1, wherein the array comprises optical waveguide cores having a cross sectional dimension between about 0.1 μ

m and about 10 μ

m.

6. The device of claim 1, wherein the array comprises at least 10 optical waveguide cores.

7. The device of claim 1, wherein at least two or more of the optical waveguide cores are optically coupled to an originating waveguide that is optically coupled to the excitation radiation source.

8. The device of claim 1, further comprising at least two excitation radiation sources optically coupled to the optical waveguide cores to pass excitation light therethrough, each of the two excitation radiation sources providing light of a different spectrum.

9. The device of claim 1, further comprising a mask layer disposed over the first surface of the substrate, wherein the mask layer comprises a plurality of apertures disposed therethrough, each aperture providing an illumination volume within which one of the optically-resolvable molecular complexes is immobilized.

10. The device of claim 9, wherein portions of the mask layer lacking the apertures block the evanescent field emanating from the array.

11. The device of claim 9, wherein the apertures are optical confinements.

12. The device of claim 9, wherein the mask layer is aligned with an optical train.

13. The device of claim 1, wherein the optically resolvable molecular complexes are immobilized on the first surface such that a signal one of them is optically resolvable from other signals from other optically resolvable molecular complexes so immobilized on the first surface.

14. The device of claim 13, wherein the optically resolvable molecular complexes are immobilized via interaction with a reaction component that is bound to the first surface.

15. The device of claim 14, wherein the reaction component comprises an enzyme.

16. The device of claim 15, wherein the enzyme is a polymerase.

17. The device of claim 1, wherein the optically resolvable molecular complexes comprise an individual analyte comprising a fluorescent or fluorogenic label that emits a signal in response to the excitation light.

18. A method of detecting a signal from an analyte, comprising:

providing a substrate comprising

a) a first surface;

b) at least a first optical waveguide proximal to the first surface;

c) a plurality of optically resolvable individual enzymes immobilized upon the first surface sufficiently proximal to the first optical waveguide to be illuminated by an evanescent field emanating from the first optical waveguide;

exposing the first surface to an analyte comprising a fluorescent or fluorogenic moiety that emits a signal in response to the evanescent field;

directing light through the first optical waveguide such that the evanescent field from the waveguide illuminates the individual enzymes; and

upon interaction of the analyte with one of the individual enzymes, detecting a signal from the analyte.

19. The method of claim 18, wherein the individual enzymes are immobilized within confined reaction volumes.

20. The method of claim 19, wherein the confined reaction volumes are within apertures in a mask layer disposed over the first surface.

21. The method of claim 20, wherein the mask layer blocks the evanescent field above portions of the substrate that are not disposed beneath one of the apertures.

22. The method of claim 20, wherein the apertures are optical confinements.

23. The method of claim 20, wherein the mask layer has a higher index of refraction than does the substrate.

24. The method of claim 18, wherein the individual enzymes are polymerase enzymes in a complex with a target nucleic acid sequence and a primer sequence complementary to a portion of the target sequence;

and wherein the analyte is a nucleotide or nucleotide analog.

25. The method of claim 18, wherein the substrate comprises an array of optical waveguides within the first surface such that at least a portion of each of the optical waveguide cores is disposed beneath the first surface of the substrate.

26. The method of claim 25, wherein each of the optical waveguides is exposed at the first surface of the substrate.

27. The method of claim 18, wherein the fluorescent or fluorogenic moiety is removed from the analyte during the interaction.

28. The method of claim 18, wherein the substrate comprises a plurality of optical waveguides proximal to the first surface, wherein the plurality includes the first optical waveguide, and further wherein the plurality is optically coupled to an originating waveguide that is optically coupled to an excitation radiation source.

29. The method of claim 18, further comprising optically coupling at least two excitation radiation sources to the first optical waveguide and passing excitation light therethrough, each of the two excitation radiation sources having different characteristics.

30. A method of determining a nucleotide sequence of a template nucleic acid, the method comprising:

providing a substrate comprising a first surface and at least a first optical waveguide proximal to the first surface of the substrate;

immobilizing an optically resolvable polymerase enzyme in a confined reaction volume on the first surface sufficiently proximal to the first optical waveguide to be illuminated by an evanescent field emanating from the first optical waveguide, wherein the polymerase enzyme is further bound to the template nucleic acid, which is further bound to a primer;

directing light through the first optical waveguide such that the evanescent field from the waveguide illuminates the confined reaction volume;

incorporating a plurality of nucleotides into a nascent strand complementary to the template nucleic acid using template-directed synthesis catalyzed by the polymerase enzyme, wherein for each of the nucleotides incorporated into the nascent strand, an identity of a base comprised therein is determined by detecting a signal produced by said each of the nucleotides when exposed to the evanescent field, thereby determining a nucleotide sequence of the nascent strand; and

determining a complementary nucleotide sequence that is complementary to the nucleotide sequence of the nascent strand, wherein the complementary nucleotide sequence is the nucleotide sequence of the template nucleic acid.

31. The method of claim 30, wherein a plurality of optically resolvable polymerase enzymes are immobilized in a plurality of confined reaction volumes.

32. The method of claim 30, wherein the incorporating is done in real time without the use of terminator chemistries.