IP Library › Granted Patent US 10,260,090
Granted Patent B2
US 10,260,090 · App. 15/213,194 · Granted Apr 16, 2019

Accelerated isothermal amplification of DNA

Inventors: Rhett L. Martineau (Gilbert, AZ); Shih-hui Chao (Phoenix, AZ); Weimin Gao (Chandler, AZ); Shufang Ci (Tempe, AZ); Deirdre R. Meldrum (Phoenix, AZ)
Assignee: ARIZONA BOARD OF REGENTS ON BEHALF OF ARIZONA STATE UNIVERSITY
C12Q1/6844
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Quick Facts
Patent No.
US 10,260,090
App. No.
15/213,194
Granted
Apr 16, 2019
Kind
B2
Abstract

A method of synthesizing a nucleic acid complementary to a target nucleic acid sequence in a template nucleic acid includes annealing a swarm primer to a target nucleic acid, the swarm primer overlapping an F1 site of the target nucleic acid and extends toward the F2 site of the target nucleic acid. An inner primer may also be annealed to the target nucleic acid to produce a complimentary nucleic acid having a single-strand loop onto which further primers may anneal. A plurality of amplicons may be reproduced, many of which may have further primers annealed thereto to generate more complementary nucleic acids.

Claims (39)

1. A method of synthesizing a nucleic acid complementary to a target nucleic acid sequence in a template nucleic acid, the method comprising:

providing a target nucleic acid having a 5′ side having an F1 site and an F2 site, and a 3′ side having a B1C site and a B2C site;

annealing a swarm primer to said target nucleic acid, wherein said swarm primer overlaps said F1 site;

initiating polymerase extension of said swarm primer toward said F2 site; and

conducting a loop-mediated isothermal amplification of said target nucleic acid.

2. The method of claim 1 , wherein said target nucleic acid comprises a first loop at said 5′ side wherein said 5′ side includes an F1C site complementary to and annealing to said F1 site to form said first loop.

3. The method of claim 1 , wherein said target nucleic acid comprises a second loop at said 3′ side wherein said 3′ includes a B1 site complementary to and annealing to said B1C site to form said second loop.

4. The method of claim 2 , further comprising annealing a first loop primer to said first loop and extending said first loop primer.

5. The method of claim 3 , further comprising annealing a second loop primer to said second loop and extending said second loop primer.

6. The method of claim 1 , wherein said swarm primer is an oligonucleotide primer.

7. The method of claim 1 , further comprising annealing a first inner primer to said B2C site, said first inner primer substantially overlapping said B2C site, and extending said inner primer toward said B1C site.

8. The method of claim 1 , further comprising annealing a second swarm primer onto a second 5′ side of said target nucleic acid, said second 5′ side having a B1 site and B2 site, wherein said second swarm primer substantially overlaps said B1 site.

9. The method of claim 1 , further comprising annealing a displacement primer to a B3C site of said target nucleic acid, and extending said displacement primer toward said B2C site.

10. The method of claim 1 , wherein said target nucleic acid comprises one or more single-stranded loops.

11. The method of claim 10 , further comprising annealing a stem primer to said single-stranded loop.

12. The method of claim 1 , further comprising reproducing a plurality of single-strand loop amplicons.

13. The method of claim 12 , further comprising repeatedly reproducing at least one of said single-stranded loop amplicons.

14. The method of claim 10 , further comprising reproducing a plurality of stem-loop amplicons.

15. The method of claim 1 , further comprising reproducing a plurality of double-stranded amplicons.

16. The method of claim 1 , further comprising reproducing a plurality of double-loop amplicons.

17. The method of claim 1 , further comprising reproducing a plurality of swarm amplicons.

18. The method of claim 1 , further comprising conducting a strand displacement reaction.

19. A method of synthesizing a nucleic acid complementary to a target nucleic acid sequence in a template nucleic acid, the method comprising:

providing a target nucleic acid having a 5′ side having an F1 site and an F2 site, and a 3′ side having a B1C site and a B2C site;

annealing a swarm primer to said target nucleic acid, wherein said swarm primer overlaps said F1 site;

initiating polymerase extension of said swarm primer toward said F2 site;

annealing a first inner primer having a primer B2 site and a primer B1C site to said target nucleic acid, wherein said inner primer overlaps said B2C site;

initiating polymerase extension of said first inner primer toward said B1C site of said target nucleic acid and synthesizing a complementary nucleic acid comprising a complementary sequence of said target nucleic acid;

conducting a strand displacement reaction to displace said complementary nucleic acid from said target nucleic acid.

20. A method of synthesizing a nucleic acid complementary to a target nucleic acid sequence in a template nucleic acid, the method comprising:

providing a target nucleic acid having a 5′ side having an F1 site and an F2 site, and a 3′ side having a B1C site and a B2C site;

annealing a swarm primer to said target nucleic acid, wherein said swarm primer substantially overlaps said F1 site;

initiating polymerase extension of said swarm primer toward said F2 site;

annealing a first inner primer having a primer B2 site and a primer B1C site to said target nucleic acid, wherein said inner primer substantially overlaps said B2C site;

initiating polymerase extension of said first inner primer toward said B1C site of said target nucleic acid and synthesizing a complementary nucleic acid comprising a complementary sequence of said target nucleic acid;

synthesizing a single-loop amplicon;

annealing a second inner primer to said single-loop amplicon;

initiating polymerase extension of said second inner primer and synthesizing a second complementary nucleic acid comprising a complementary sequence of said single-loop amplicon;

conducting a strand displacement reaction to displace said second complementary nucleic acid from said single-loop amplicon.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 22, 2019
From: MELDRUM, DEIRDRE; GAO, WEIMIN; CI, SHUFANG; CHAO, SHIH-HUI; MARTINEAU, RHETT
To: ARIZONA BOARD OF REGENTS ON BEHALF OF ARIZONA STATE UNIVERSITY
Reel/Frame 048410/0076 →
Continuity (2)
Provisional Application 62193205 · Jul 16, 2015
Related Publication 20170107549A1 · Apr 20, 2017