Pyrophosphorolytic sequencing

Patent metadata

Field	Value
Publication number	US-10450605-B2
Application number	US-201715847362-A
Country	US
Kind code	B2
Filing date	Dec 19, 2017
Priority date	May 24, 2013
Publication date	Oct 22, 2019
Grant date	Oct 22, 2019

Abstract

A method for determining the sequence of a target nucleic acid, including steps of contacting a target nucleic acid with a polymerase to sequentially remove nucleotide triphosphates from the target nucleic acid, wherein the nucleotide triphosphates that are removed have a variety of different base moieties; and distinguishing the different base moieties for the nucleotide triphosphates that are removed. Also provided is a apparatus including a nanopore positioned in a fluid impermeable barrier to form a passage through which a nucleotide triphosphate can pass from a first fluid reservoir to a second fluid reservoir, and a reaction mix in the first fluid reservoir that includes a polymerase, target nucleic acid having two strands, and pyrophosphorolytic concentration of pyrophosphate.

First claim

What is claimed is:

1. A method for determining the sequence of a target nucleic acid, comprising:
(a) providing a target nucleic acid having two strands;
(b) contacting the target nucleic acid with a polymerase under conditions to sequentially remove nucleotides from a first strand of the two strands by pyrophosphorolysis, thereby sequentially producing single nucleotide triphosphates having a variety of different base moieties, wherein the conditions to sequentially remove single nucleotide triphosphates from a first strand of the two strands by pyrophosphorolysis comprise contacting the polymerase with a pyrophosphorolytic concentration of pyrophosphate; and
(c) distinguishing the variety of different base moieties for the sequentially produced single nucleotide triphosphates, wherein the distinguishing of the variety of different base moieties for the sequentially produced single nucleotide triphosphates comprises passing the single nucleotide triphosphates through a nanopore and distinguishing the single nucleotide triphosphates by detecting variations in an ionic current flowing through the nanopore, thereby determining the sequence of the target nucleic acid, wherein the pyrophosphorolysis is paused and then resumed between (b) and (c), to produce the single nucleotide triphosphates at a desired rate.

2. The method of claim 1 , wherein the polymerase is attached to the nanopore.

3. The method of claim 1 , wherein the nanopore comprises a protein nanopore that is embedded in a membrane.

4. The method of claim 3 , wherein a second strand of the two strands of the target nucleic acid is attached to the membrane.

5. The method of claim 1 , wherein the nanopore comprises a solid state nanopore.

6. The method of claim 1 , wherein the pyrophosphorolytic concentration of pyrophosphate comprises a concentration of at least 100 μM.

7. The method of claim 1 , wherein the pausing the sequential removal of the single nucleotide triphosphates is by removing pyrophosphate from contact with the polymerase and then resuming the sequential removal of the single nucleotide triphosphates is by contacting the polymerase with pyrophosphate.

8. The method of claim 1 , wherein the variety of different base moieties comprises at least two different species of base moieties and at most four different species of base moieties.

9. The method of claim 8 , wherein the sequence that is determined is longer than four nucleotides.

10. The method of claim 1 , wherein the variety of different base moieties comprise naturally occurring adenine, guanine, cytosine or thymine.

11. The method of claim 1 , wherein at least one of the variety of different base moieties comprises a moiety that is non-naturally occurring in DNA or RNA.

12. The method of claim 1 , wherein the target nucleic acid is DNA.

13. The method of claim 12 , wherein at least one of the variety of different base moieties comprises a moiety that is non-naturally occurring in DNA.

14. The method of claim 12 , wherein at least one of the variety of different base moieties comprises 5-methyl cytosine or 5-hydroxymethylcytosine.

15. The method of claim 14 , wherein the 5-methyl cytosine or 5-hydroxymethylcytosine is distinguished from cytosine, thereby facilitating an epigenetic analysis.

16. The method of claim 1 , wherein the polymerase lacks 3′ to 5′ exonuclease activity.

17. The method of claim 1 , wherein the target nucleic acid is a heteroduplex formed by a DNA strand and RNA strand.

18. The method of claim 1 , wherein the conditions to sequentially remove nucleotide triphosphates from one of the two strands by pyrophosphorolysis comprise contacting the polymerase with a pyrophosphorolytic concentration of a pyrophosphate analog.

19. The method of claim 18 , wherein the pyrophosphate analog comprises pyrophosphate having an additional moiety.

20. The method of claim 18 , wherein the pyrophosphate analog comprises pyrovanadate.

21. The method of claim 1 , wherein at least 10 nucleotides are sequentially removed from the first strand of two strands and distinguished by passing through the nanopore.

Assignees

• Illumina Cambridge Ltd

Inventors

• Meuleman Wouter

Classifications

• C12Q1/6869 Primary

  Methods for sequencing · CPC title

• C12Q2565/631

  being a biochannel or pore · CPC title

• C12Q2521/525

  Phosphatase · CPC title

• C12Q2521/319

  Exonuclease · CPC title