Nucleic acid sequencing by Raman monitoring of uptake of nucleotides during molecular replication

• US 20050202468A1
• Filed: 12/23/2004
• Published: 09/15/2005
• Est. Priority Date: 12/30/2003
• Status: Abandoned Application

• Current Assignee: Intel Corporation
• Original Assignee: Intel Corporation
• Inventors: Su, Xing, Sun, Lei, Berlin, Andrew, Koo, Tae-Woong, Chan, Selena, Sundararajan, Narayanan
• Application Number:
  US11/020,776
• Publication Number:
  US 20050202468A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: C12Q 1/6869 Methods for sequencing
• CPC Class Codes: C12Q 2533/101 Primer extension
• CPC Class Codes: C12Q 2565/632 being a surface enhanced, e.g. resonance, Raman spectrometer
• CPC Class Codes: G01N 21/658 enhancement Raman, e.g. surface plasmons

Abstract

The methods and apparatus disclosed herein are useful for detecting nucleotides, nucleosides, and bases and for nucleic acid sequence determination. The methods involve detection of a nucleotide, nucleoside, or base using surface enhanced Raman spectroscopy (SERS) or surface enhanced coherent anti-Stokes Raman spectroscopy (SECARS). The detection can be part of a nucleic acid sequencing reaction to detect uptake of a deoxynucleotide triphosphate during a nucleic acid polymerization reaction, such as a nucleic acid sequencing reaction. The nucleic acid sequence of a synthesized nascent strand, and the complementary sequence of the template strand, can be determined by tracking the order of incorporation of nucleotides during the polymerization reaction. Methods for enhancing the SERS signal of a nucleotide or nucleoside by cleaving the base from a sugar moiety are provided. Furthermore, methods for detecting single base repeats are provided.

Claims

1. A method to detect a nucleotide or nucleoside, comprising:

a) separating a purine or pyrimidine base from a ribose or deoxyribose moiety of the nucleotide or nucleoside;

b) depositing the separated purine base or pyrimidine base on a surface enhanced Raman spectroscopy (SERS) substrate; and

c) detecting the separated purine or pyrimidine base using SERS.

2. The method of claim 1, wherein the method detects a deoxynucleotide triphosphate.

3. The method of claim 2, wherein the method further comprises including the deoxynucleotide triphosphate in a nucleic acid sequencing reaction mixture before separating the purine or pyrimidine base from the purine or pyrimidine moiety.

4. The method of claim 1, wherein the purine or pyrimidine base is associated with a Raman label before it is detected by SERS.

5. The method of claim 1, wherein the nucleotide or nucleoside comprises a purine base.

6. The method of claim 5, wherein the base consists essentially of adenine.

7. The method of claim 5, wherein the base consists essentially of guanine.

8. The method of claim 1, wherein the surface enhanced Raman spectroscopy is surface enhanced coherent anti-Stokes Raman spectroscopy (SECARS).

9. The method of claim 8, wherein the nucleotide or nucleoside comprises a pyrimidine base.

10. The method of claim 9, wherein the nucleotide or nucleoside comprises thymine.

11. The method of claim 9, wherein the nucleotide or nucleoside comprises uracil.

12. The method of claim 9, wherein the nucleotide or nucleoside comprises cytosine.

13. The method of claim 1, wherein the target molecule is deposited on silver nanoparticles.

14. The method of claim 13, wherein the target molecule is contacted with an alkali-metal halide salt.

15. The method of claim 14, wherein the alkali-metal halide salt is lithium chloride.

16. A method to detect a target molecule comprising a purine base or a pyrimidine base, comprising:

a) isolating the target molecule;

b) depositing the target molecule on a surface enhanced Raman spectroscopy (SERS) substrate;

c) detecting Raman scattering from the irradiated target molecule using surface enhanced coherent anti-Stokes Raman spectroscopy (SECARS), thereby detecting the target molecule.

17. The method of claim 16, wherein the target molecule is isolated from a biological sample.

18. The method of claim 16, wherein the target molecule is a nucleotide, a nucleoside, or a base.

19. The method of claim 18, wherein the target molecule consists essentially of a pyrimidine base.

20. The method of claim 19, wherein the base consists essentially of thymine.

21. The method of claim 19, wherein the base consists essentially of uracil.

22. The method of claim 19, wherein the base consists essentially of a cytidine.

23. The method of claim 16, wherein the target molecule is a nucleotide triphosphate.

24. A method to detect identical nucleotides at consecutive target positions in a template nucleic acid molecule, comprising:

a) contacting a known number of copies of the template nucleic acid molecule with a reaction mixture comprising a primer, a polymerase, and a known initial concentration of a first nucleotide to form a post-reaction mixture, the primer or the template nucleic acid being immobilized on a surface of the reaction chamber, wherein the 3′

terminus of the primer binds to the template nucleic acid molecule upstream of a 5′

nucleotide of the consecutive target positions;

b) depositing the post-reaction mixture on a surface enhanced Raman spectroscopy (SERS) substrate;

c) detecting the first nucleotide using SERS; and

d) determining whether more than one first nucleotide was added to the consecutive target positions.

25. The method of claim 24, wherein the known number of copies of the template nucleic acid molecule is about the same as a known number of first nucleotide molecules in the reaction mixture.

26. The method of claim 24, wherein the known number of copies of the template nucleic acid molecule is about one half a known number of first nucleotide molecules in the reaction mixture.

27. The method of claim 24, further comprising adding additional first nucleotide to the reaction mixture after detecting the first nucleotide.

28. The method of claim 24, further comprising cleaving a base from the nucleotide and detecting the base using SERS.

29. The method of claim 24, wherein the SERS detection is surface enhanced coherent anti-Stokes Raman spectroscopy (SECARS).

30. The method of claim 24, further comprising repeating steps a-d with a different nucleotide.

31. The method of claim 24, wherein the nucleotide is attached to a Raman label before it is detected by SERS.

32. The method of claim 24, wherein an internal control is included in the reaction mixture and detected using SERS.

33. The method of claim 32, wherein the SERS signal of the internal control and the nucleotide is compared to determine whether more than one nucleotide was added to the consecutive target positions.

34. A method to determine a nucleotide occurrence at a target position of a template nucleic acid molecule, comprising:

a) contacting a detectable number of template nucleic acids with a reaction mixture in a reaction chamber, the reaction mixture comprising a primer, a polymerase, and an initial concentration of a first nucleotide triphosphate, the primer or the template nucleic acid being immobilized on a surface of the reaction chamber;

b) incubating the reaction mixture to allow binding of the primer to the template nucleic acid and formation of a post-reaction mixture;

c) depositing the post reaction mixture, or a component thereof, on a surface enhanced Raman spectroscopy (SERS) substrate; and

d) detecting a Raman signal from the first nucleotide using SERS, wherein a decrease in intensity of the Raman signal of the first nucleotide in the post-reaction mixture identifies an extension reaction product, thereby identifying the nucleotide occurrence at the target position.

35. The method of claim 34, further comprising repeating steps a-d with a different nucleotide until the nucleotide occurrence is identified.

36. The method of claim 35, further comprising washing the substrate before optionally repeating steps a-d.

37. The method of claim 34, wherein the incubation time is about 1 second to 10 minutes.

38. The method of claim 34, wherein the reaction chamber is less than 100 nm in at least one dimension.

39. The method of claim 34, wherein a pre-reaction SERS analysis is performed on the first nucleotide before it contacts the template nucleic acid molecule.

40. The method of claim 39, wherein a decrease in intensity of the SERS signal of the first nucleotide in the post-reaction mixture compared to the pre-reaction mixture identifies the extension reaction product.

41. The method of claim 34, wherein the method is performed twice for the target nucleotide position, using dATP and dGTP one at a time as the first nucleotide and a second nucleotide.

42. The method of claim 41, wherein the complementary strand of the template nucleic acid molecule is immobilized in a second reaction chamber and the method is performed an additional two times, again using dATP and dGTP one at a time as the first nucleotide and the second nucleotide.

43. The method of claim 34, wherein an internal control is included in the reaction mixture and detected using SERS.

44. The method of claim 43, wherein the SERS signal of the internal control and the nucleotide is compared to identify the nucleotide occurrence at the target position.