Method and system employing distinguishable polymerases for detecting ternary complexes and identifying cognate nucleotides

Patent metadata

Field	Value
Publication number	US-11248254-B2
Application number	US-201715851383-A
Country	US
Kind code	B2
Filing date	Dec 21, 2017
Priority date	Dec 30, 2016
Publication date	Feb 15, 2022
Grant date	Feb 15, 2022

Abstract

Method of identifying a cognate nucleotide (i.e., the “next correct nucleotide”) for a primed template nucleic acid molecule. In some embodiments, an ordered or random array of primed target nucleic acids characterized by different cognate nucleotides can be evaluated using a single imaging step to identify different cognate nucleotides for a collection of different primed template nucleic acid molecules. An optional incorporation step can follow the identifying step. A polymerase different from the ones used in the binding and examination steps can be used to incorporate a nucleotide, such as a reversible terminator nucleotide, preliminary to identification of the next cognate nucleotide.

First claim

What is claimed is:

1. A method of distinguishing a first primed template nucleic acid from a second primed template nucleic acid in a first mixture, comprising
(a) providing a first mixture comprising a population of different primed template nucleic acids attached to a solid support and a first stabilized ternary complex, the first stabilized ternary complex comprising a first primed template nucleic acid of the first mixture, a polymerase attached to a first type of label, and a first type of nucleotide;
(b) removing any unbound polymerase attached to the first type of label from the first mixture, thereby forming a second mixture;
(c) forming a second stabilized ternary complex by contacting the second mixture with a first reagent comprising a second type of nucleotide and a polymerase attached to a second type of label that is different from the first type of label, the second stabilized ternary complex comprising a second primed template nucleic acid of the first mixture, the polymerase of the first reagent, and the second type of nucleotide of the first reagent, thereby forming a third mixture comprising the first stabilized ternary complex and the second stabilized ternary complex, wherein the second type of nucleotide is different from the first type of nucleotide;
(d) removing any unbound polymerase attached to the second type of label from the third mixture, thereby forming a fourth mixture; and
(e) distinguishing the first primed template nucleic acid from the second primed template nucleic acid in the first mixture by detecting, in the fourth mixture, the first type of label and the second type of label.

2. The method of claim 1 , wherein the first type of label is covalently attached to the polymerase of the first stabilized ternary complex.

3. The method of claim 2 , wherein the second type of label is covalently attached to the polymerase of the second stabilized ternary complex.

4. The method of claim 1 , wherein the first type of nucleotide and the second type of nucleotide are not distinguishably labeled with respect to each other.

5. The method of claim 4 , wherein both the first type of nucleotide and the second type of nucleotide are unlabeled nucleotides.

6. The method of claim 1 , wherein step (b) comprises contacting the first mixture with a wash solution comprising the first type of nucleotide.

7. The method of claim 1 , wherein step (d) comprises contacting the third mixture with a wash solution comprising the first type of nucleotide and the second type of nucleotide.

8. The method of claim 1 , wherein the first reagent further comprises the first type of nucleotide.

9. The method of claim 1 , wherein the first type of nucleotide is not covalently attached to the first primed template nucleic acid in the first stabilized ternary complex of the second mixture, and wherein the second type of nucleotide is not covalently attached to the second primed template nucleic acid in the second stabilized ternary complex of the fourth mixture.

10. The method of claim 1 , further comprising
(f) forming a third stabilized ternary complex by contacting the fourth mixture with a second reagent comprising a third type of nucleotide and a polymerase attached to a third type of label that is different from the first type of label and the second type of label, the third stabilized ternary complex comprising a third primed template nucleic acid of the first mixture, the polymerase of the second reagent, and the third type of nucleotide of the second reagent, thereby forming a fifth mixture comprising the first stabilized ternary complex, the second stabilized ternary complex and the third stabilized ternary complex;
(g) removing any unbound polymerase attached to the third type of label from the fifth mixture, thereby forming a sixth mixture; and
(h) distinguishing the third primed template nucleic acid from the first primed template nucleic acid and the second primed template nucleic acid in the first mixture by detecting, in the sixth mixture, the third type of label.

11. The method of claim 10 , wherein the third type of label is covalently attached to the polymerase of the third stabilized ternary complex.

12. The method of claim 10 , wherein the first type of nucleotide, the second type of nucleotide and the third type of nucleotide are not distinguishably labeled with respect to each other.

13. The method of claim 10 , wherein step (g) comprises contacting the fifth mixture with a wash solution comprising the first type of nucleotide, the second type of nucleotide and the third type of nucleotide.

14. The method of claim 10 , wherein the second reagent further comprises the second type of nucleotide.

15. The method of claim 10 , wherein the first type of nucleotide is not covalently attached to the first primed template nucleic acid in the first stabilized ternary complex of the sixth mixture; wherein the second type of nucleotide is not covalently attached to the second primed template nucleic acid in the second stabilized ternary complex of the sixth mixture, and wherein the third type of nucleotide is not covalently attached to the third primed template nucleic acid in the third stabilized ternary complex of the sixth mixture.

16. The method of claim 10 , further comprising
(i) forming a fourth stabilized ternary complex by contacting the sixth mixture with a third reagent comprising a fourth type of nucleotide and a polymerase attached to a fourth type of label that is different from the first type of label, the second type of label and the third type of label, the fourth stabilized ternary complex comprising a fourth primed template nucleic acid of the first mixture, the polymerase of the third reagent, and the fourth type of nucleotide of the third reagent, thereby forming a seventh mixture comprising the first stabilized ternary complex, the second stabilized ternary complex, third stabilized ternary complex and the fourth stabilized ternary complex;
(j) removing any unbound polymerase attached to the fourth type of label from the seventh mixture, thereby forming an eighth mixture; and
(k) distinguishing the fourth primed template nucleic acid from the first primed template nucleic acid, the second primed template nucleic acid and the third primed template nucleic acid in the first mixture by detecting, in the eighth mixture, the fourth type of label.

17. The method of claim 16 , wherein the fourth type of label is covalently attached to the polymerase of the fourth stabilized ternary complex.

18. The method of claim 16 , wherein the first type of nucleotide, the second type of nucleotide, the third type of nucleotide and the fourth type of nucleotide are not distinguishably labeled with respect to each other.

19. The method of claim 16 , wherein step (j) comprises contacting the seventh mixture with a wash solution comprising the first type of nucleotide, the second type of nucleotide, the third type of nucleotide and the fourth type of nucleotide.

20. The method of claim 16 , wherein the third reagent further comprises the third type of nucleotide.

21. The method of claim 16 , wherein the first type of nucleotide is not covalently attached to the first primed template nucleic acid in the first stabilized ternary complex of the eighth mixture; wherein the second type of nucleotide is not covalently attached to the second primed template nucleic acid in the second stabilized ternary complex of the eighth mixture, wherein the third type of nucleotide is not covalently attached to

Assignees

• Omniome Inc

Inventors

• Dambacher Corey M
• Cayer Devon
• Lecoultre Richard
• Rokicki Joseph
• Wilson Kerry
• Tu Eugene
• Vijayan Kandaswamy

Classifications

• C12Q1/6827 Primary

  for detection of mutation or polymorphism · CPC title

• C12Q1/6869

  Methods for sequencing · CPC title

• C12Q1/6874

  involving nucleic acid arrays, e.g. sequencing by hybridisation · CPC title

• C12Q1/6816 Primary

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

• C12Q2535/125

  Allele specific primer extension · CPC title