Polymerase idling method for single molecule DNA sequencing

Patent metadata

Field	Value
Publication number	US-9546398-B2
Application number	US-201414538632-A
Country	US
Kind code	B2
Filing date	Nov 11, 2014
Priority date	Nov 14, 2013
Publication date	Jan 17, 2017
Grant date	Jan 17, 2017

Abstract

A method for sequencing a nucleic acid is provided. In certain embodiments the method comprises obtaining a duplex comprising a nucleic acid and a primer, wherein the primer has a nuclease resistant 3′ end, combining the duplex with a chain terminator nucleotide and a proof-reading polymerase to produce a reaction in which the polymerase idles on the added chain terminator nucleotide, identifying the chain terminator nucleotide added to the end of the primer; and adding a nuclease-resistant nucleotide to the end of the primer after the polymerase has idled on and removed the added chain terminator nucleotide, thereby producing a duplex comprising the template and an extended primer that has a nuclease resistant 3′ end.

First claim

What is claimed is:

1. A method of sequencing, comprising:
(a) obtaining a duplex comprising a nucleic acid and a primer, wherein the primer has a nuclease resistant 3′ end;
(b) combining the duplex with a chain terminator nucleotide, a 3′ to 5′ exonuclease activity, and a DNA polymerase activity to produce an idling reaction in which the polymerase activity repeatedly adds the chain terminator nucleotide onto the end of the primer using the nucleic acid as a template and the 3′ to 5′ exonuclease activity repeatedly removes the chain terminator nucleotide;
(c) identifying the chain terminator nucleotide repeatedly added to the end of the primer;
(d) adding a nuclease-resistant nucleotide to the end of the primer, thereby producing a duplex comprising said template and an extended primer that has a nuclease resistant 3′ end, wherein the chain terminator nucleotide has a higher probability of being incorporated than the nuclease-resistant nucleotide; and
(e) repeating steps (b) and (c) on the product of step (d), thereby determining the sequence of two consecutive nucleotides of the nucleic acid.

2. The method of claim 1 , wherein the nuclease-resistant nucleotide of (d) is a reversible chain terminator nucleotide and wherein the method comprises, after step (d), removing a blocking moiety from the nuclease resistant nucleotide before repeating step (b).

3. The method of claim 1 , further comprising repeating steps (b), (c) and (d) at least 10 times, thereby determining the sequence of at least 10 consecutive nucleotides in the nucleic acid.

4. The method of claim 1 , wherein the method comprises quantifying how much chain terminator nucleotide is repeatedly added to the end of the primer by the polymerase activity in the idling reaction.

5. The method of claim 1 , wherein the combining step (b) comprises combining the duplex with a single chain terminator nucleotide corresponding to G, A, T or C.

6. The method of claim 5 , wherein the identifying step comprises detecting pyrophosphate release.

7. The method of claim 5 , wherein the identifying step comprises direct or indirect detection of protons.

8. The method of claim 5 , wherein the chain terminator nucleotide is a phosphate labeled fluorescent nucleotide and the identifying step comprises reading fluorescence.

9. The method of claim 5 , wherein the chain terminator nucleotide comprises a charge blockade label, and the identifying step comprises use of a nanopore.

10. The method of claim 1 , wherein:
the combining step (b) comprises combining the duplex with four chain terminators corresponding to G, A, T and C, wherein the four chain terminators comprise different distinguishable labels; and
the identifying step (c) comprises identifying which of the four chain terminator nucleotides is added to the end of the primer.

11. The method of claim 1 , wherein the nuclease-resistant nucleotide contains a phosphorothioate.

12. The method of claim 1 , wherein the duplex is DNA that comprises single stranded regions and double stranded regions, that has been stretched on a substrate.

13. The method of claim 12 , wherein the duplex is in a nanofluidic channel on a substrate.

14. The method of claim 12 , wherein the duplex is made by: nicking a double stranded DNA at one or more sites, making single stranded gaps in the double stranded DNA using an exonuclease, adding an nuclease resistant reversible terminator onto 3′ ends adjacent to the gaps, and then deprotecting the added nuclease resistant reversible terminator nucleotides.

15. The method of claim 1 , wherein the DNA polymerase activity and the 3′ to 5′ exonuclease activity are provided by a proofreading polymerase.

16. The method of claim 10 , wherein the identifying step (c) comprises use of a nanopore.

17. The method of claim 1 , wherein the nucleic acid or the primer is immobilized on a solid support.

18. The method of claim 1 , wherein the combining step (b) comprises a pyrophosphorolysis reaction.

Assignees

• Agilent Technologies Inc

Inventors

• Peter Brian Jon
• Mannion John
• Myerson Joel

Classifications

• C12Q1/6834

  Enzymatic or biochemical coupling of nucleic acids to a solid phase · CPC title

• C12Q1/6816

  characterised by the detection means (C12Q1/6804 takes precedence) · CPC title

• C12Q1/6869 Primary

  Methods for sequencing · CPC title

• C12Q2525/186

  incorporating a non-extendable or blocking moiety · CPC title

• C12Q2525/125

  incorporating agents resulting in resistance to degradation · CPC title