IP Library Granted Patent US 8,637,243
Granted Patent B2
US 8,637,243 · App. 13/722,497 · Granted Jan 28, 2014

Methods for nucleic acid manipulation

Inventors: Stephen J Benkovic (State College, PA); Frank Salinas (Wheaton, IL)
Assignee: The Penn State Research Foundation
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Quick Facts
Patent No.
US 8,637,243
App. No.
13/722,497
Granted
Jan 28, 2014
Kind
B2
Abstract

A method for replicating and amplifying a target nucleic acid sequence is described. A method of the invention involves the formation of a recombination intermediate without the prior denaturing of a nucleic acid duplex through the use of a recombination factor. The recombination intermediate is treated with a high fidelity polymerase to permit the replication and amplification of the target nucleic acid sequence. In preferred embodiments, the polymerase comprises a polymerase holoenzyme. In further preferred embodiments, the recombination factor is bacteriophage T4 UvsX protein or homologs from other species, and the polymerase holoenzyme comprises a polymerase enzyme, a clamp protein and a clamp loader protein, derived from viral, bacteriophage, prokaryotic, archaebacterial, or eukaryotic systems.

Claims (22)

1. A composition for amplifying a target nucleic acid sequence comprising: (a) bacteriophage UvsX protein; (b) two primers that are complementary to the ends of said target nucleic acid sequence, said primers present in a molar excess relative to said target nucleic acid sequence; (c) a polymerase; and (d) nucleotides in an amount sufficient to support amplification of said target nucleic acid sequence.

2. A composition according to claim 1 , further comprising a UvsX protein accessory factor.

3. A composition according to claim 1 , wherein said polymerase is a polymerase holoenzyme.

4. A composition according to claim 3 , wherein said polymerase holoenzyme comprises a polymerase enzyme, a clamp protein, and a clamp loader protein.

5. A composition according to claim 1 , further comprising a single stranded nucleic acid binding protein.

6. A composition according to claim 1 , further comprising a helicase.

7. A method for amplifying a target nucleic acid comprising contacting said target nucleic acid sequence with the composition of claim 1 .

8. A composition for amplifying a target nucleic acid sequence comprising: (a) bacteriophage UvsX protein; (b) two primers that are complementary to the ends of said target nucleic acid sequence; (c) a prokaryotic polymerase; and (d) nucleotides in an amount sufficient to support amplification of said target nucleic acid sequence.

9. A composition according to claim 8 , further comprising a UvsX protein accessory factor.

10. A composition according to claim 8 , wherein said polymerase is a polymerase holoenzyme.

11. A composition according to claim 10 , wherein said polymerase holoenzyme comprises a polymerase enzyme, a clamp protein, and a clamp loader protein.

12. A composition according to claim 8 , further comprising a single stranded nucleic acid binding protein.

13. A composition according to claim 8 , further comprising a helicase.

14. A method for amplifying a target nucleic acid comprising contacting said target nucleic acid sequence with the composition of claim 8 .

15. A composition for amplifying a target nucleic acid sequence comprising: (a) bacteriophage UvsX protein; (b) a UvsX protein accessory factor; (c) two primers that are complementary to the ends of said target nucleic acid sequence; (c) a polymerase, and (d) nucleotides in an amount sufficient to support amplification of said target nucleic acid sequence.

16. A composition for amplifying a target DNA sequence comprising: (a) bacteriophage UvsX protein; (b) two primers that are complementary to the ends of said target nucleic acid sequence; and (c) a prokaryotic polymerase.

17. A composition according to claim 16 , further comprising a UvsX protein accessory factor.

18. A composition according to claim 16 , wherein said polymerase is a polymerase holoenzyme.

19. A composition according to claim 18 , wherein said polymerase holoenzyme comprises a polymerase enzyme, a clamp protein, and a clamp loader protein.

20. A composition according to claim 16 , further comprising a single stranded nucleic acid binding protein.

21. A composition according to claim 16 , further comprising a helicase.

22. A method for amplifying a target nucleic acid comprising contacting said target nucleic acid sequence with the composition of claim 16 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 14, 2013
From: BENKOVIC, STEPHEN J; SALINAS, FRANK
To: THE PENN STATE RESEARCH FOUNDATION
Reel/Frame 030617/0816 →
CONFIRMATORY LICENSE Recorded Jan 25, 2013
From: THE PENNSYLVANIA STATE UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 029698/0273 →
Continuity (5)
Continuation 12786053 · May 24, 2010
Continuation 11204125 · Aug 15, 2005
Continuation 10125973 · Apr 19, 2002
Provisional Application 60285127 · Apr 20, 2001
Related Publication 20130137145A1 · May 30, 2013