Recombinase polymerase amplification
View Patent ↗This disclosure describes related novel methods for Recombinase-Polymerase Amplification (RPA) of a target DNA that exploit the properties of recombinase and related proteins, to invade double-stranded DNA with single stranded homologous DNA permitting sequence specific priming of DNA polymerase reactions. The disclosed methods have the advantage of not requiring thermocycling or thermophilic enzymes. Further, the improved processivity of the disclosed methods may allow amplification of DNA up to hundreds of megabases in length.
1. A composition comprising:
(1) at least one recombinase;
(2) at least one polymerase;
(3) a target nucleic acid;
(4) a crowding agent; and
(5) a first nucleic acid primer and optionally a second nucleic acid primer.
2. The composition of claim 1 , wherein the at least one recombinase is selected from the group consisting of UvsX, RecA, and combinations thereof.
3. The composition of claim 1 , wherein the at least one polymerase includes at least one DNA polymerase which lacks 3′-5′ exonuclease activity.
4. The composition of claim 1 , wherein the at least one polymerase comprises a DNA polymerase with strand displacing properties.
5. The composition of claim 1 , wherein the crowding agent is present at a concentration between 1 to 12% of a weight or a volume of the composition.
6. The composition of claim 1 , wherein the crowding agent is selected from the group consisting of polyethylene glycols, dextran, ficoll and a combination thereof.
7. The composition of claim 6 , wherein the crowding agent comprises polyethylene glycol at a concentration between 1 to 12% of a weight or a volume of the composition.
8. The composition of claim 6 , wherein said polyethylene glycol is selected from the group consisting of PEG1450, PEG3000, PEG8000, PEG10000, PEG compound (molecular weight 15,000 to 20,000), and combinations thereof.
9. The composition of claim 1 , wherein the first and second nucleic acid primers are selected from the group consisting of DNA, RNA, PNA, LNA, morpholino backbone nucleic acid, phosphorothiorate backbone nucleic acid, and a combination thereof.
10. The composition of claim 1 , further comprising at least one recombinase loading protein.
11. The composition of claim 10 , wherein the recombinase loading protein is selected from the group consisting of T4 uvsY, E. coli recO, E. coli recR and combinations thereof.
12. The composition of claim 10 , wherein the recombinase loading protein is present at a concentration of between 0.2 μM and 8 μM.
13. The composition of claim 1 , wherein the at least one polymerase is selected from the group consisting of prokaryotic polymerase, eukaryotic polymerase and phage-encoded polymerase.
14. The composition of claim 13 , wherein said eukaryotic polymerase is selected from the group consisting of pol-α, pol-β, pol-δ, and a combination thereof.
15. The composition of claim 13 , wherein the procaryotic polymerase is selected from the group consisting of E. coli DNA polymerase I Klenow fragment, bacteriophage T4 gp43 DNA polymerase, Bacillus stearothermophilus polymerase I large fragment, Phi-29 DNA polymerase, T7 DNA polymerase, Bacillus subtilis Pol I large fragment (Bsu polymerase), E. coli DNA polymerase I, E. coli DNA polymerase II, E. coli DNA polymerase III, E. coli DNA polymerase IV, E. coli DNA polymerase V and a combination thereof.
16. The composition of claim 1 , wherein the recombinase is in contact with the first nucleic acid primer to form a nucleoprotein primer.
17. The composition of claim 1 , wherein the composition comprises a first nucleic acid primer and a second nucleic acid primer.
18. The composition of claim 17 , further comprising a third nucleic acid primer.
19. The composition of claim 18 , further comprising a fourth nucleic acid primer.
20. The composition of claim 17 , wherein the recombinase is in contact with the nucleic acid primers to form a first and a second nucleoprotein primer.
21. The composition of claim 1 , wherein the recombinase is temperature-sensitive.
22. The composition of claim 1 , further comprising at least one single stranded DNA binding protein.
23. The composition of claim 22 , wherein said single stranded DNA binding protein is selected from the group consisting of E. coli SSB, T4 gp32 and combinations thereof.
24. The composition of claim 1 , further comprising ATP or an ATP analog.
25. The composition of claim 1 , further comprising dNTPs or a mixture of dNTPs and ddNTPs.
26. The composition of claim 1 , further comprising a buffer.
27. The composition of claim 1 , wherein the target nucleic acid comprises a double stranded target sequence.
28. The composition of claim 1 , wherein the target nucleic acid comprises a single stranded target sequence.
29. The composition of claim 16 , wherein the first nucleic acid primer comprises a 3′ blocking group.
30. The composition of claim 18 , wherein at least one primer comprises a 3′ blocking group.
31. A kit comprising:
(1) at least one recombinase;
(2) at least one polymerase; and
(3) a crowding agent.
32. The kit of claim 31 , further comprising a first nucleic acid primer and optionally a second nucleic acid primer.
33. The kit of claim 31 , further comprising dNTPs or a mixture of dNTPs and ddNTPs.
34. The kit of claim 31 , further comprising a buffer, and/or ATP or ATP analog.
35. The kit of claim 31 , further comprising a third primer and optionally a fourth primer.
36. The kit of claim 31 , wherein the crowding agent is selected from the group consisting of polyethylene glycols, dextran, ficoll and a combination thereof.
37. A reagent mixture for nucleic acid amplification comprising:
(1) at least one recombinase;
(2) at least one polymerase; and
(3) a crowding agent.
38. The reagent mixture of claim 37 , further comprising dNTPs or a mixture of dNTPs and ddNTPs.
39. The reagent mixture of claim 37 , further comprising a buffer, and/or ATP or ATP analog.
40. A composition comprising: the reagent mixture of claim 37 ; a target nucleic acid; and at least one nucleic acid primer.