Arrays of optical confinements and uses thereof

• US 7,315,019 B2
• Filed: 09/16/2005
• Issued: 01/01/2008
• Est. Priority Date: 09/17/2004
• 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, Korlach, Jonas
• Primary Examiner(s): Wells; Nikita
• Application Number:
  US11/228,759
• Publication Number:
  US 20060061754A1
• Time in Patent Office: 837 Days
• Field of Search: None
• US Class Current: 250/251
• CPC Class Codes: B01L 2200/0668 Trapping microscopic beads
• CPC Class Codes: B01L 2300/0654 Lenses; Optical fibres
• CPC Class Codes: B01L 2300/0896 Nanoscaled
• CPC Class Codes: B01L 3/5085 for multiple samples, e.g. microtitration plates
• CPC Class Codes: B82Y 20/00 Nanooptics, e.g. quantum optics or photonic crystals
• CPC Class Codes: B82Y 30/00 Nanotechnology for materials or surface science, e.g. nanocomposites
• CPC Class Codes: C12Q 1/6869 Methods for sequencing
• CPC Class Codes: C12Q 2521/101 DNA polymerase
• CPC Class Codes: C12Q 2521/543 Immobilised enzyme(s)
• CPC Class Codes: C12Q 2561/113 Real time assay
• CPC Class Codes: C12Q 2565/537 characterised by the capture oligonucleotide acting as a primer
• CPC Class Codes: G01N 21/6452 Individual samples arranged in a regular 2D-array, e.g. multiwell plates
• CPC Class Codes: G02B 6/13 Integrated optical circuits characterised by the manufacturing method
• CPC Class Codes: Y10T 436/10 Composition for standardization, calibration, simulation, stabilization, preparation or preservation; processes of use in preparation for chemical testing

Abstract

The present invention relates to optical confinements, methods of preparing and methods of using them for analyzing molecules and/or monitoring chemical reactions. The apparatus and methods embodied in the present invention are particularly useful for high-throughput and low-cost single-molecular analysis.

Claims

1. An apparatus comprising:

an array of waveguides on a solid support, said array having a fill fraction greater than about 0.0001, wherein said waveguides are suitable for holding a biological reagent, and wherein said waveguides provide an effective observation volume that permits observation of individual molecules present in said biological reagent; and

an optical system operatively coupled to the waveguides that detects signals from the effective observation volume of said waveguides.

2. The apparatus of claim 1, wherein said array has a fill fraction greater than about 0.001.

3. The apparatus of claim 1, wherein said array has a fill fraction greater than about 0.01.

4. The apparatus of claim 1, wherein said array has a fill fraction greater than about 0.1.

5. The apparatus of claim 1, wherein said array has a fill fraction ranging from about 0.001 to about 0.1.

6. The apparatus of claim 1, wherein said biological reagent comprises an enzyme, and substrates of said enzyme present at a concentration of about Michaelis constant (Km) of said enzyme for said substrates.

7. The apparatus of claim 6, wherein said concentration is higher than about 1 micromolar.

8. The apparatus of claim 6, wherein said concentration is higher than about 50 micromolar.

9. The apparatus of claim 6, wherein said concentration is higher than about 100 micromolar.

10. The apparatus of claim 6, wherein said substrates are labeled.

11. The apparatus of claim 6, wherein said individual molecules are products of a reaction between said enzyme and said substrates contained in said biological reagent.

12. The apparatus of claim 1, wherein said individual molecules are DNA/polymerase complexes.

13. The apparatus of claim 1, wherein said individual molecules are biomolecules selected from the group consisting of nucleic acids, polypeptides, and combinations thereof.

14. The apparatus of claim 1, wherein said individual molecules are organic or inorganic chemical compounds.

15. The apparatus of claim 1, wherein said individual molecules are labeled with a detectable label.

16. The apparatus of claim 15, wherein said detectable label is selected from the group consisting of a fluorescent label, a chemiluminescent label, and a radioactive label.

17. The apparatus of claim 1, wherein said waveguides are made of porous film.

18. The apparatus of claim 1, wherein said waveguides are operatively coupled to an optical transmission element transmitting an incident light beam.

19. The apparatus of claim 18, wherein said optical transmission element comprises an element selected from the group consisting of a microlens, a nanolens, an arrayed waveguide grating, an optical switch, an optical fiber, an optical attenuator, a polarization filter, a wave plate, and a delay line.

20. The apparatus of claim 1, wherein said optical system further comprises a photon detector.

21. The apparatus of claim 20, wherein said photon detector is selected from the group consisting of an optical reader, a high efficiency photon detection system, a photodiode, a camera, a charge coupled device, an electron-multiplying charge coupled device, and an intensified charge coupled device.

22. The apparatus of claim 1 that precludes propagation of a majority of an incident electromagnetic energy having a wavelength greater than a cutoff wavelength.

23. The apparatus of claim 22, wherein an individual waveguide of said array comprises a cladding surrounding a core, and wherein said individual waveguide precludes propagation of more than 90% of the incident electromagnetic energy having a wavelength greater than a cutoff wavelength through said core.

24. The apparatus of claim 22, wherein an individual waveguide of said array comprises a cladding surrounding a core, and wherein said individual waveguide precludes propagation of more than 99% of the incident electromagnetic energy having a wavelength greater than a cutoff wavelength through said core.

25. The apparatus of claim 23, wherein each individual waveguide of said array comprises a cladding surrounding a core, and wherein said individual waveguide precludes propagation of more than 90% of the incident electromagnetic energy having a wavelength greater than a cutoff wavelength through said core.

26. The apparatus of claim 22, wherein said cladding comprises a sheet, and one or more holes extending through said sheet where each hole constitutes a core of an individual waveguide.

27. The apparatus of claim 22, wherein an individual waveguide of said array comprises a cladding surrounding a core that is cylindrical.

28. The apparatus of claim 22, wherein an individual waveguide of said array comprises a cladding surrounding a core that is non-cylindrical.

29. The apparatus of claim 22, wherein said cladding comprises a metal alloy.

30. The apparatus of claim 1, wherein each individual waveguide provides an effective observation volume less than about 1000 zeptoliters.

31. The apparatus of claim 1, wherein each individual waveguide provides an effective observation volume less than about 80 zeptoliters.

32. The apparatus of claim 1, wherein each individual waveguide provides an effective observation volume less than about 10 zeptoliters.

33. A kit comprising an array of waveguides of claim 1 and an instruction manual for use of said array.

34. A method of performing multiple chemical reactions involving a plurality of reaction samples, comprising:

(a) providing an array of waveguides of claim 1;

(b) placing the plurality of reaction samples comprising labeled reactants into the waveguides in the array, wherein a separate reaction sample is placed into a different waveguide in the array;

(c) subjecting the array to conditions suitable for formation of products of the chemical reactions; and

(d) detecting the formation of the products with said optical system.

35. The method of claim 34, wherein the step of detecting comprises illuminating the different waveguides with an incident light beam and detecting an optical signal emitted from the reaction samples.

36. The method of claim 34, wherein the chemical reactions involve protein-protein interactions.

37. The method of claim 34, wherein the chemical reactions involve nucleic acid-protein interactions.

38. The method of claim 34, wherein the chemical reactions involve nucleic acid-nucleic acid interactions.

39. A method of detecting a biological analyte, comprising:

optically capturing the analyte within an optical confinement that is created by

(a) providing an array of waveguides having a fill fraction greater than about 0.0001; and

(b) illuminating at least one waveguide within the array that is suspected to contain the analyte with an incident light beam thereby detecting the analyte.

40. The method of claim of claim 39, said array of waveguides having a fill fraction from about 0.001 to about 0.1.

41. The method of claim 39, wherein said fill fraction is greater than about 0.1.

42. The method of claim 39, wherein the analyte is labeled with a detectable label.

43. The method of claim 39, wherein the analyte is selected from the group consisting of nucleic acid, polypeptide, organic compound, and inorganic compound.

44. A method of sequencing a plurality of target nucleic acid molecules, comprising:

(a) providing an array of waveguides having a fill fraction greater than about 0.0001;

(b) mixing in the waveguides the plurality of target nucleic acid molecules, primers complementary to the target nucleic acid molecules, polymerization enzymes, and more than one type of nucleotides or nucleotide analogs to be incorporated into a plurality of nascent nucleotide strands, each strand being complementary to a respective target nucleic acid molecule;

(c) subjecting the mixture of step (b) to a polymerization reaction under conditions suitable for formation of the nascent nucleotide strands by template-directed polymerization of the nucleotides or nucleotide analogs;

(d) illuminating the waveguides with an incident light beam; and

(e) identifying the nucleotides or the nucleotide analogs incorporated into the each nascent nucleotide strand.

45. The method of claim 44, wherein the step of identifying yields a time sequence of incorporation of the nucleotides provided in step (b).

46. The method of claim 44, wherein the identifying step is effected while the template-directed polymerization is taking place.

47. The method of claim 44, wherein the target nucleic acid molecules are selected from the group consisting of circular DNA molecules, linear DNA molecules, RNA molecules, and DNA/RNA hybrids.