Intermittent detection during analytical reactions

Patent metadata

Field	Value
Publication number	US-9556480-B2
Application number	US-201514708603-A
Country	US
Kind code	B2
Filing date	May 11, 2015
Priority date	Mar 28, 2008
Publication date	Jan 31, 2017
Grant date	Jan 31, 2017

Abstract

Methods, devices, and systems for performing intermittent detection during analytical reactions are provided. Such methods facilitate collection of reaction data from disparate reaction times. Further, such methods are useful for reducing photo-induced damage of one or more reactants in an illuminated analytical reaction at a given reaction time. In preferred embodiments, the reaction mixture is subjected to at least one illuminated and non-illuminated period and allowed to proceed such that the time in which the reaction mixture is illuminated is less than a photo-induced damage threshold period.

First claim

What is claimed is:

1. A method of performing a nucleic acid sequencing reaction, comprising:
a) preparing a reaction mixture comprising components of the nucleic acid sequencing reaction including a polynucleotide to be sequenced;
b) initiating the nucleic acid sequencing reaction in the reaction mixture to begin progression of the nucleic acid sequencing reaction, wherein the nucleic acid sequencing reaction is initiated during a non-illuminated period, and wherein the reaction mixture comprises an enzyme selected from the group consisting of: a polymerase, a ligase, a ribosome, a nuclease, and a kinase; and
c) maintaining conditions that allow the nucleic acid sequencing reaction to proceed while subjecting the reaction mixture to at least one illuminated period following the non-illuminated period, wherein illumination data is collected during the at least one illuminated period, thereby performing the nucleic acid sequencing reaction.

2. The method of claim 1 , wherein the at least one illuminated period is followed by a second non-illuminated period.

3. The method of claim 1 , wherein the nucleic acid sequencing reaction proceeds during multiple illuminated and non-illuminated periods.

4. The method of claim 1 , wherein the non-illuminated period and the at least one illuminated period are created without any substitution of components in the nucleic acid sequencing reaction during progression of the nucleic acid sequencing reaction.

5. The method of claim 1 , wherein the nucleic acid sequencing reaction generates a plurality of noncontiguous sequence reads from the single nucleic acid template.

6. The method of claim 1 , wherein the nucleic acid sequencing reaction is a single-molecule sequencing reaction.

7. The method of claim 1 , wherein the nucleic acid sequencing reaction is a template-directed sequencing reaction.

8. The method of claim 1 , wherein the illumination data is collected in real time during the nucleic acid sequencing reaction.

9. The method of claim 1 , wherein the reaction mixture further comprises multiple optically detectable components that are distinguishable from one another based upon their individual signal emissions during the at least one illuminated period.

10. The method of claim 9 , wherein the multiple optically detectable components comprise luminescent, fluorescent, or fluorogenic labels.

11. The method of claim 1 , wherein a plurality of nucleic acid sequencing reactions are performed, and further wherein the plurality of nucleic acid sequencing reactions are disposed on a solid support.

12. The method of claim 1 , wherein the nucleic acid sequencing reaction generates sequence reads during the at least one illuminated period and does not generate sequence reads during the non-illuminated period.

13. The method of claim 1 , wherein the polynucleotide is a double-stranded nucleic acid comprising a first hairpin linker connecting a 3′ terminus of a first strand of the double-stranded nucleic acid with a 5′ terminus of a second strand of the double-stranded nucleic acid, and a second hairpin linker connecting a 5′ terminus of the first strand of the double-stranded nucleic acid with a 3′ terminus of the second strand of the double-stranded nucleic acid.

14. The method of claim 13 , wherein the first hairpin linker is identical to the second hairpin linker.

15. The method of claim 13 , wherein the first hairpin linker is not identical to the second hairpin linker.

16. The method of claim 13 , wherein at least one of the first hairpin linker and the second hairpin linker comprises a primer binding site, registration sequence, or a synthesis blocking moiety.

17. The method of claim 1 , wherein the nucleic acid sequencing reaction generates redundant sequence data.

18. The method of claim 1 , wherein the nucleic acid sequencing reaction comprises primer extension by a polymerase and the illumination data comprises a sequence of nucleobases incorporated into a nascent strand by the polymerase during the at least one illuminated period.

19. The method of claim 1 , wherein a region of the polynucleotide subjected to the nucleic acid sequencing reaction during the non-illuminated period comprises at least about 100 adjacent nucleotide positions.

20. A method of performing a nucleic acid sequencing reaction, comprising:
a) preparing a reaction mixture comprising components of the nucleic acid sequencing reaction including a polynucleotide to be sequenced;
b) initiating the nucleic acid sequencing reaction in the reaction mixture to begin progression of the nucleic acid sequencing reaction, wherein the nucleic acid sequencing reaction is initiated during a non-illuminated period; and
c) maintaining conditions that allow the nucleic acid sequencing reaction to proceed while subjecting the reaction mixture to multiple illuminated periods following the non-illuminated period, wherein illumination data is collected during the multiple illuminated periods to generate a plurality of noncontiguous sequence reads from the single nucleic acid template, thereby performing the nucleic acid sequencing reaction.

Assignees

• Pacific Biosciences California Inc

Inventors

• Turner Stephen
• Sorenson Jon
• Maxham Kenneth Mark
• Eid John

Classifications

• G01N33/48721

  Investigating individual macromolecules, e.g. by translocation through nanopores (Coulter counters in general G01N15/12; fabrication methods for nanoscale apertures B81B1/00; sequencing of nucleic acids C12Q1/68) · CPC title

• G16B30/00

  ICT specially adapted for sequence analysis involving nucleotides or amino acids · CPC title

• C12Q1/6869 Primary

  Methods for sequencing · CPC title

• C12N9/1252

  DNA-directed DNA polymerase (2.7.7.7), i.e. DNA replicase · CPC title

• G01N2021/6439

  with indicators, stains, dyes, tags, labels, marks · CPC title