Two slow-step polymerase enzyme systems and methods

• US 8,133,672 B2
• Filed: 03/30/2009
• Issued: 03/13/2012
• Est. Priority Date: 03/31/2008
• Status: Active Grant

• Current Assignee: Pacific Bioscience of California Incorporated (L'Oreal SA)
• Original Assignee: Pacific Bioscience of California Incorporated (L'Oreal SA)
• Inventors: Bjornson, Keith, Lee, Harold, Korlach, Jonas, Turner, Stephen, Bibillo, Arek, Christians, Fred, Emig, Robin, He, Molly, Park, Insil, Jia, Lei, Fedorov, Andrei, Lyle, John
• Primary Examiner(s): Strzelecka, Teresa E
• Application Number:
  US12/414,191
• Publication Number:
  US 20090286245A1
• Time in Patent Office: 1,079 Days
• Field of Search: None
• US Class Current: 435/6.1
• CPC Class Codes: C12Q 1/6869 Methods for sequencing
• CPC Class Codes: C12Q 1/6874 involving nucleic acid arrays, e.g. sequencing by hybridisation
• CPC Class Codes: C12Q 2521/101 DNA polymerase
• CPC Class Codes: C12Q 2527/101 Temperature
• CPC Class Codes: C12Q 2527/119 pH
• CPC Class Codes: C12Q 2527/125 Specific component of sample, medium or buffer
• CPC Class Codes: C12Q 2527/137 Concentration of a component of medium
• CPC Class Codes: C12Q 2565/1015 labels being on the same oligonucleotide

Abstract

Compositions, kits, methods and systems for nucleotide sequencing comprising producing polymerase reactions that exhibit two kinetically observable steps within an observable phase of the polymerase reaction. Two slow step systems can be produced, for example, by selecting the appropriate polymerase enzyme, polymerase reaction conditions including cofactors, and polymerase reaction substrates including the primed template and nucleotides.

Claims

1. A method for nucleotide sequencing comprising:

a) providing a reaction mixture having;

(i) a polymerase enzyme, (ii) polymerase reaction conditions including cofactors, and (iii) polymerase reaction substrates including a primed template and nucleotides, such that a reaction comprising incorporation of the nucleotides into a growing nucleic acid occurs; and

b) observing the reaction mixture to determine the incorporation of nucleotides into the growing nucleic acid;

wherein the polymerase enzyme, the polymerase reaction conditions, and the polymerase reaction substrates are selected such that the reaction exhibits two kinetically observable steps, each of which kinetically observable steps proceeds from an intermediate in which a nucleotide or a polyphosphate product is bound to the polymerase enzyme or each of which kinetically observable steps proceeds from an intermediate in which the nucleotide and the polyphosphate product are not bound to the polymerase enzyme, and

c) using the observed incorporation of nucleotides to determine a sequence of the template.

2. The method of claim 1 wherein the two kinetically observable steps are each steps which proceed from an intermediate in which a nucleotide or a polyphosphate product is bound to the polymerase enzyme.

3. The method of claim 1 wherein the two kinetically observable steps are each steps which proceed from an intermediate in which the nucleotide and the polyphosphate product are not bound to the polymerase enzyme.

4. (Withdrawn, Currently Amended) The method of claim 1 wherein the reaction exhibits two kinetically observable steps which proceed from an intermediate in which a nucleotide or a polyphosphate product is bound to the polymerase enzyme, and two kinetically observable steps which proceed from an intermediate in which the nucleotide and the polyphosphate product are not bound to the polymerase enzyme.

6. The method of claim 1 wherein the two kinetically observable steps are template translocation and nucleotide binding.

7. The method of claim 1 wherein the ratio of the rate constants of the kinetically observable steps is from 2:

1 to 1;

2.

8. The method of claim 1 wherein the rate constant for one of the kinetically observable steps is less than about 100 per second.

9. The method of claim 1 wherein the rate constant for one of the kinetically observable steps is between about 0.1 per second and about 60 per second.

10. The method of claim 1 wherein the rate constant for one of the kinetically observable steps is between about 1 per second and about 20 per second.

11. The method of claim 1 wherein the reaction exhibits more than two kinetically observable steps in an observable phase.

12. The method of claim 1 wherein the polymerase enzyme comprises a modified recombinant Φ

29-type polymerase.

13. The method of claim 12 wherein the polymerase enzyme comprises a modified recombinant Φ

29, B103, GA-1, PZA, Φ

15, BS32, M2Y, Nf, G1, Cp-1, PRD1, PZE, SF5, Cp-5, Cp-7, PR4, PR5, PR722, or L17 polymerase.

14. The method of claim 12 wherein the polymerase enzyme comprises a modified recombinant Φ

29 DNA polymerase having at least one amino acid substitution or combination of substitutions selected from the group consisting of;

an amino acid substitution at position 484, an amino acid substitution at position 198, and an amino acid substitution at position 381.

15. The method of claim 12 wherein the polymerase enzyme comprises a modified recombinant Φ

29 DNA polymerase having at least one amino acid substitution or combination of substitutions selected from the group consisting of E375Y, K512Y, T368F, A484E, A484Y, N387L, T372Q, T372L, K478Y, 1370W, F198W, and L381A.

16. The method of claim 1 wherein the polymerase reaction conditions comprise one or more of metal cofactor concentration, pH, temperature, an enzyme activity modulator, D20, an organic solvent, and buffer.

17. The method of claim 16 wherein the polymerase reaction conditions comprise a mixture of divalent metal ions comprising at least one catalytic metal ion and at least one non-catalytic metal ion.

18. The method of claim 17 wherein the catalytic metal is selected from Mg2+, Mn2+ and mixtures thereof, and the non-catalytic metal is selected from Ca2+, Zn2+, Co2+, Ni2+, Eu2+, Sr2+, Ba2+, Fe2+, Eu2+ and mixtures thereof.

19. The method of claim 17 wherein a ratio of catalytic metal to non-catalytic metal in the reaction mixture is from about 10:

1 to about 1;

10.

20. The method of claim 16 wherein the polymerase reaction conditions comprise the presence of D2O.

21. The method of claim 20 wherein the D2O/H2O volume ratio in the reaction mixture is about 0.1 to about 2.

22. The method of claim 16 wherein the conditions comprise an organic solvent selected from the group consisting of ethanol, methanol, THF, dioxane, DMA, DMF, and DMSO.

23. The method of claim 22 wherein the solvent comprises DMA.

24. The method of claim 22 wherein the solvent comprises DMSO.

25. The method of claim 1 wherein the polymerase conditions comprise an additive that when added, changes the polymerase enzyme kinetics relative to a reaction having no additive.

26. The method of claim 25 wherein the additive is a thiol containing amino acid.

27. The method of claim 26 wherein the additive is L-cysteine.

28. The method of claim 1 wherein the nucleotide comprises one, two, or three non-bridging thiol groups in its polyphosphate portion.

29. The method of claim 28 wherein the nucleotide has one non-bridging thiol.

30. The method of claim 29 wherein substantially only one chiral isomer is used.

31. The method of claim 1 wherein the polymerase substrate that is selected such that the reaction exhibits two kinetically observable steps comprises a modified primer-template nucleotide complex.

5. The method of claim I wherein the two kinetically observable steps are selected from a group consisting of enzyme isomerization, nucleotide incorporation, and product release.