Sequencing methods using enzyme conformation

• US 8,911,972 B2
• Filed: 12/14/2010
• Issued: 12/16/2014
• Est. Priority Date: 12/16/2009
• Status: Active Grant

• Current Assignee: Pacific Bioscience of California Incorporated (L'Oreal SA)
• Original Assignee: Pacific Bioscience of California Incorporated (L'Oreal SA)
• Inventors: Chaisson, Mark, Clark, Sonya, Silk, Christopher, Lyle, John, Jia, Lei, Bjornson, Keith
• Primary Examiner(s): Pande, Suchira
• Application Number:
  US12/967,507
• Publication Number:
  US 20110160077A1
• Time in Patent Office: 1,463 Days
• Field of Search: None
• US Class Current: 435/91.2
• CPC Class Codes: C12Q 1/6869 Methods for sequencing
• CPC Class Codes: C12Q 2521/101 DNA polymerase
• CPC Class Codes: C12Q 2561/113 Real time assay
• CPC Class Codes: C12Q 2563/107 fluorescence
• CPC Class Codes: C12Q 2565/133 conformational analysis

Abstract

Systems and methods are provided for single-molecule sequencing of template nucleic acids in which the signal from a label attached to a polymerase enzyme is used to monitor conformational changes in the polymerase which occur while labeled nucleotides or nucleotide analogs are added to a growing nucleic acid chain which is complementary to the template nucleic acid. The signal indicative of the conformational state of the enzyme is used to determine with higher confidence when true nucleotide or nucleotide analog incorporation events occur, allowing for the improved quality of base calls and sequence determination.

Claims

1. A method of sequencing comprising;

providing a single polymerase enzyme complex comprising a polymerase enzyme, a nucleic acid template, and a primer;

wherein the polymerase enzyme comprises a label which has a signal that changes when the enzyme undergoes a conformational change corresponding to translocation;

contacting the complex with sequencing reagents including two or more types of nucleotides or nucleotide analogs, each labeled with a different label, whereby enzyme mediated addition of nucleotides or nucleotide analogs to the primer to produce a growing strand complementary to the template occurs, wherein the labels on each of the two or more types of nucleotides or nucleotide analogs, and the label on the polymerase enzyme each provide a distinct signal;

monitoring in real time the distinct signals from the labels on each of the two or more types of nucleotides or nucleotide analogs, and the distinct signals from the label on the polymerase enzyme as the growing strand is produced;

determining the type of nucleotide or nucleotide analog that has been incorporated by observing signals from the labeled nucleotides or nucleotide analogs during the enzyme mediated addition;

determining whether a nucleotide or nucleotide analog is incorporated into the growing strand using observed signals from the labeled polymerase enzyme that are indicative of translocation; and

combining the determination of the type of nucleotide or nucleotide analog with the determination of whether a nucleotide or nucleotide analog is incorporated, whereby observing both a signal from the label on a type of nucleotide or nucleotide analog and a signal from the label on the polymerase enzyme corresponding to translocation within the same time period indicates that a nucleotide or nucleotide analog of that type has been incorporated in that time period, and whereby observing only a signal from the label on a type of nucleotide or nucleotide analog, and no signal from the label on the polymerase enzyme corresponding to translocation within the same time period indicates that no nucleotide or nucleotide analog has been incorporated in that time period, to obtain more accurate sequencing than without the determination of whether a nucleotide or nucleotide analog has been incorporated, whereby including the signals from the labeled polymerase reduces errors due to branching.

2. The method of claim 1 wherein the labels for the enzyme and the nucleotides or nucleotide analogs comprise fluorescent labels.

3. The method of claim 1 wherein the signal that changes when the enzyme undergoes a conformational change comprises a FRET signal from a donor and an acceptor.

4. The method of claim 3 wherein the donor and acceptor are both attached to the polymerase enzyme.

5. The method of claim 4 wherein the donor and acceptor are attached to portions of the enzyme which move relative to one another during a conformational change.

6. The method of claim 1 wherein the label whose signal changes when the enzyme undergoes a conformational change comprises a fluorescent label whose fluorescence is sensitive to changes in its local environment.

7. The method of claim 1 wherein the signal that changes when the enzyme undergoes a conformational change comprises quenching of a fluorescent label.

8. The method of claim 7 wherein the polymerase enzyme has both a fluorescent label and a quencher attached to different portions of the enzyme, and the quenching results from relative motions of the different portions of the enzyme from a conformational change.

9. The method of claim 1 wherein the polymerase enzyme comprises a DNA polymerase or an RNA polymerase.

10. The method of claim 9 wherein the template comprises DNA or RNA.

11. The method of claim 9 wherein the polymerase is a modified Type B polymerase.

12. The method of claim 1 wherein at least one label is attached to the fingers, palm, thumb, or exo domains.

13. A method for nucleic acid sequencing comprising:

providing a reaction mixture for nucleic acid polymerization comprising four types of nucleotides or nucleotide analogs, each having a different label;

contacting the reaction mixture with a polymerase enzyme complex comprising a polymerase enzyme, a template nucleic acid, and a primer;

under conditions whereby enzyme mediated addition of nucleotides or nucleotide analogs to produce a growing nucleic acid strand from the primer occurs, wherein the enzyme comprises a label which exhibits a change in optical properties when the enzyme undergoes a conformational change corresponding to translocation, wherein the label on the enzyme provides a distinct signal to the labels on the four types of nucleotide or nucleotide analogs;

observing optical signals from the nucleotides or nucleotide analog and the enzyme while the nucleotides or nucleotide analogs are incorporated into the growing nucleic acid strand;

determining, using the observed optical signal from the nucleotides or nucleotide analogs, when a particular type of nucleotide or nucleotide analog is associated with the enzyme;

determining, using the observed optical signal from the label on the enzyme, when the enzyme undergoes a conformational change corresponding to translocation;

using the determination of when a particular nucleotide or nucleotide analog is associated with the enzyme to measure which type of nucleotide or nucleotide analog is incorporated in combination with the determination of when the enzyme undergoes conformational change corresponding to translocation to measure whether a nucleotide or nucleotide analog has been incorporated, to obtain a nucleic acid sequence of the template, whereby observing both a signal from the label on a type of nucleotide or nucleotide analog and a signal from the label on the polymerase enzyme corresponding to translocation within the same time period indicates that a nucleotide or nucleotide analog of that type has been incorporated in that time period, and whereby observing only a signal from the label on a type of nucleotide or nucleotide analog, and no signal from the label on the polymerase enzyme corresponding to translocation within the same time period indicates that no nucleotide or nucleotide analog has been incorporated in that time period, whereby including the determination of when the enzyme undergoes conformational change reduces errors due to branching.

14. The method of claim 13 wherein the labels for the enzyme and for the nucleotides or nucleotide analogs comprise fluorescent labels.

15. The method of claim 13 wherein the signal that changes when the enzyme undergoes a conformational change comprises a FRET signal from a donor and an acceptor.

16. The method of claim 15 wherein the donor and acceptor are both attached to the polymerase enzyme.

17. The method of claim 16 wherein the donor and acceptor are attached to portions of the enzyme which move relative to one another during a conformational change.

18. The method of claim 13 wherein the label whose signal changes when the enzyme undergoes a conformational change comprises a fluorescent label whose fluorescence is sensitive to changes in its local environment.