Methods for multiplexing recombinase polymerase amplification

• US 8,062,850 B2
• Filed: 07/25/2006
• Issued: 11/22/2011
• Est. Priority Date: 07/25/2005
• Status: Active Grant

• Current Assignee: Abbott Diagnostics Scarborough, Inc. (Abbott Laboratories Incorporated)
• Original Assignee: Alere San Diego Incorporated (Abbott Laboratories Incorporated)
• Inventors: Armes, Niall A., Piepenburg, Olaf, Williams, Colin H.
• Primary Examiner(s): CHUNDURU, SURYAPRABHA
• Application Number:
  US11/988,825
• Publication Number:
  US 20090269813A1
• Time in Patent Office: 1,946 Days
• Field of Search: 435/6, 435/91.2, 536/24.33
• US Class Current: 435/6.12
• CPC Class Codes: C12N 15/113 Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing when used in plants C12N15/8218
• CPC Class Codes: C12Q 1/6804 Nucleic acid analysis using immunogens immunoassay G01N33/53
• CPC Class Codes: C12Q 1/6816 characterised by the detection means C12Q1/6804 takes precedence
• CPC Class Codes: C12Q 1/6827 for detection of mutation or polymorphism
• CPC Class Codes: C12Q 1/6844 Nucleic acid amplification reactions
• CPC Class Codes: C12Q 1/6853 using modified primers or templates
• CPC Class Codes: C12Q 2521/301 Endonuclease
• CPC Class Codes: C12Q 2521/507 Recombinase
• CPC Class Codes: C12Q 2525/119 incorporating abasic sites
• CPC Class Codes: C12Q 2525/125 incorporating agents resulting in resistance to degradation
• CPC Class Codes: C12Q 2537/125 Sandwich assay format
• CPC Class Codes: C12Q 2537/1376 Displacement by an enzyme
• CPC Class Codes: C12Q 2561/113 Real time assay
• CPC Class Codes: C12Q 2563/131 the label being a member of a cognate binding pair, i.e. extends to antibodies, haptens, avidin
• CPC Class Codes: C12Q 2565/101 Interaction between at least two labels
• CPC Class Codes: C12Q 2565/102 Multiple non-interacting labels
• CPC Class Codes: C12Q 2565/625 being a nucleic acid test strip device, e.g. dipsticks, strips, tapes, CD plates
• CPC Class Codes: G01N 2021/7759 Dipstick; Test strip
• CPC Class Codes: G01N 2021/7763 Sample through flow
• CPC Class Codes: G01N 2021/7793 Sensor comprising plural indicators
• CPC Class Codes: G01N 21/78 : producing a change of colour

Abstract

This disclosure provides for methods and reagents for rapid multiplex RPA reactions and improved methods for detection of multiplex RPA reaction products. In addition, the disclosure provides new methods for eliminating carryover contamination between RPA processes.

Claims

1. A process comprising:

(a) contacting a recombinase agent with first, second and third nucleic acid primers to form first, second and third nucleoprotein primers, the third nucleic acid primer being an extension blocked primer that comprises one or more modified internal residues selected from the group consisting of tetrahydrofuran residue and deoxyribose residue;

(b) contacting the first and second nucleoprotein primers to a double stranded target nucleic acid thereby forming first and second double stranded structures, the first double stranded structure being formed from the first nucleoprotein primer and a first strand of the double stranded target nucleic acid at a portion of the first strand, and the second double stranded structure being formed from the second nucleoprotein primer and a second strand of the double stranded target nucleic acid at a portion of the second strand so that 3′

ends of the first and second nucleoprotein primers are oriented toward each other on the target nucleic acid molecule with a portion of the target nucleic acid molecule between the 3′

ends of the first and second nucleoprotein primers;

(c) extending the 3′

ends of the first and second nucleoprotein primers with one or more polymerases and dNTP to generate a first amplified target nucleic acid with an internal region comprising the third portion of the target nucleic acid molecule between the 3′

ends of the first and second nucleoprotein primers;

(d) contacting the first amplified target nucleic acid with the third nucleoprotein primer in the presence of a nuclease selected from the group consisting of E. coli Nfo, E. coli exonuclease III, and fpg to form a third double stranded structure at the third portion of the amplified target nucleic acid;

the nuclease specifically cleaving the tetrahydrofuran or deoxyribose residue only after the formation of the third double stranded structure, and cleavage of the tetrahydrofuran or deoxyribose residue forming a third 5′

primer double stranded structure and a 3′

extension blocked primer double stranded structure;

(e) extending the 3′

end of the third 5′

primer with one or more polymerases and dNTP to generate a second double stranded amplified nucleic acid which comprises the first nucleic acid primer and the third 5′

primer;

(f) continuing the reaction through repetition of (b) through (e) until a desired degree of the second double stranded amplified nucleic acid is reached.

2. The process of claim 1, wherein the nuclease is E. coli Nfo or E. coli exonuclease III, and wherein the modified internal residue is a tetrahydrofuran residue.

3. The process of claim 1, wherein the nuclease is fpg, and wherein the modified internal residue is a deoxyribose residue.

4. The process of claim 1, wherein the third extension blocked primer comprises a blocked 3′

residue which is resistant to extension by DNA polymerase.

5. The process of claim 4, wherein the blocked 3′

residue comprises a blocking moiety which prevents the extension of the primer by polymerase.

6. The process of claim 5, wherein the blocking moiety is attached to the 3′

or 2′

site of the 3′

residue sugar.

7. The process of claim 5, wherein the blocking moiety is a detectable label.

8. The process of claim 7, wherein the detectable label is selected from the group consisting of a fluorophore, an enzyme, a quencher, an enzyme inhibitor, a radioactive label, a member of a binding pair, and a combination thereof.

9. The process of claim 4, wherein the blocked 3′

residue comprises a dideoxy nucleotide.

10. The process of claim 1, wherein the one or more polymerases comprise a strand-displacing polymerase.

11. The process of claim 1, wherein the first nucleic acid primer comprises a first detectable label and the third extension blocked primer comprises a second detectable label.

12. The process of claim 11, wherein the first and second detectable label are different and the production of the second double stranded amplified nucleic acid is monitored by detecting the presence of the first and second detectable label on a single double stranded DNA molecule.

13. The process of claim 12, wherein the production of the second double stranded amplified nucleic acid is detected by a sandwich assay wherein a first antibody binds the first detectable label and a second antibody binds the second detectable label.

14. The process of claim 1, wherein the third extension blocked primer further comprises one or more detectable labels.

15. The process of claim 14, wherein the process further comprises the step of monitoring the progress of the RPA reaction by detecting the detectable label on the third extension blocked primer.

16. The process of claim 14, wherein the detectable label is selected from the group consisting of a fluorophore, an enzyme, a quencher, an enzyme inhibitor, a radioactive label, one member of a binding pair and a combination thereof.

17. The process of claim 16, wherein the fluorophore is attached to the third extension blocked primer by a fluorophore-dT residue.

18. The process of claim 16, wherein the quencher is attached to the third extension blocked primer by a quencher-dT residue.

19. The process of claim 1, wherein the third extension blocked primer comprises a fluorophore and a quencher.

20. The process of claim 19, wherein the fluorophore and quencher are separated by between 0 to 2 bases.

21. The process of claim 19, wherein the fluorophore and quencher are separated by between 0 to 5 bases.

22. The process of claim 19, wherein the fluorophore and quencher are separated by between 0 to 8 bases.

23. The process of claim 19, wherein the fluorophore and quencher are separated by between 0 to 10 bases.

24. The process of claim 19, wherein the fluorophore and quencher are separated by a greater distance when the extension blocked primer is unhybridized than when the extension blocked primer is hybridized to the target nucleic acid.

25. The process of claim 19, wherein the fluorophore or the quencher is attached to the noncomplementary or modified internal residue and wherein the fluorophore and quencher are separated following cleavage of the modified internal base by the nuclease.

26. The process of claim 19, wherein the fluorophore is selected from the group of fluorescein, FAM, TAMRA.

27. The process of claim 19, wherein the quencher comprises a non-fluorescent chromophore.

28. The process of claim 27, wherein the non-fluorescent chromophore is selected from the group consisting of DEEP DARK QUENCHER 1, DEEP DARK QUENCHER 2, BLACK HOLE QUENCHER 1 and BLACK HOLE QUENCHER 2.

29. The process of claim 1, wherein the first primer, second primer or third extension blocked primer is 12 to 40 residues in length.

30. The process of claim 1, wherein the first primer, second primer or third extension blocked primer is 12 to 60 residues in length.

31. The process of claim 1, wherein the process amplifies at least the third portion of the target nucleic acid at least 10⁷ fold.

32. The process of claim 1, wherein the process is performed in the presence of 1% to 12% PEG.

33. The process of claim 1, wherein the process is performed in the presence of 6% to 8% PEG.

34. The process of claim 1, wherein the dNTP comprise dUTP and wherein the process is performed in the presence of uracil glycosylase for a first period of less than 20 minutes and wherein the process is performed in the presence of uracil glycosylase inhibitor after the first period.

35. The process of claim 34, wherein the process is performed without temperature based inactivation of the uracil glycosylase.

36. The process of claim 34, wherein the uracil glycosylase inhibitor is Bacillus subtilis phage PBS1 uracil glycosylase inhibitor or Bacillus subtilis phage PBS2 uracil glycosylase inhibitor.

37. The process of claim 34, wherein the dNTP consist of dATP, dUTP, dCTP and dGTP.

38. The process of claim 34, wherein the dNTP do not contain dTTP.

50. The process of claim 11, wherein the blocked 3′

residue comprises a blocking moiety which prevents the extension of the primer by polymerase.

51. The process of claim 50, wherein the blocking moiety is attached to the 3′

or 2′

site of the 3′

residue sugar.

39. A process comprising:

(a) contacting a recombinase agent with first, second and third nucleic acid primers to form first, second and third nucleoprotein primers, the third nucleic acid primer being an extension blocked primer that comprises a fluorophore, a quencher and a noncomplementary or modified internal residue;

(b) contacting the first and second nucleoprotein primers to a double stranded target nucleic acid thereby forming first and second double stranded structures, the first double stranded structure being between the first nucleoprotein primer and a first strand of the double stranded target nucleic acid at a portion of the first strand, and the second double stranded structure being between the second nucleoprotein primer and a second strand of the double stranded target nucleic acid at a portion of the second strand so that 3′

ends of the first and second nucleoprotein primers are oriented toward each other on the target nucleic acid molecule with a portion of the target nucleic acid molecule between the 3′

ends;

(c) extending the 3′

ends of the first and second nucleoprotein primers with one or more polymerases and dNTP to generate an amplified target nucleic acid with an internal region comprising the portion the target nucleic acid molecule between the 3′

ends;

(d) contacting the amplified target nucleic acid with the third nucleoprotein primer in the presence of a nuclease to form a third double stranded structure at a portion of the amplified target nucleic acid, the nuclease specifically cleaving the noncomplementary or modified internal residue only after formation of the third double stranded structure, and cleavage of the noncomplementary or modified internal residue separating the fluorophore and the quencher so that fluorescence of the fluorophore is detectable; and

(e) detecting the fluorescence of the fluorophore.

40. The process of claim 39, further comprising repeating (b) through (e) until a desired degree of fluorescence is detected.

41. The process of claim 39, wherein the nuclease is a DNA glycosylase or AP endonuclease.

42. The process of claim 39, wherein the modified internal residue comprises a uracil or inosine residue.

43. The process of claim 42, wherein the nuclease recognizes the uracil or inosine residue and cleaves the third primer at the uracil or inosine residue.

44. The process of claim 39, wherein the nuclease recognizes a base mismatch between the noncomplementary base of the third nucleic acid primer and the target nucleic acid and cleaves the third nucleic acid primer at the noncomplementary base.

45. The process of claim 39, wherein the nuclease is selected from the group consisting of fpg, Nth, MutY, MutS, MutM, E. coli MUG, human MUG, human Ogg, vertebrate Nei-like (Neil) glycosylases, uracil glycosylase, hypoxanthine-DNA glycosylase, and functional analogs thereof.

46. The process of claim 39, wherein the nuclease is E. coli Nfo or E. coli exonuclease III and wherein the modified residue comprises a tetrahydrofuran residue or carbon linker.

47. The process of claim 39, wherein the modified internal base is selected from the group consisting of 8-oxoguanine, thymine glycol, and abasic site mimic.

48. The process of claim 47, wherein the abasic site mimic is a tetrahydrofuran residue or D-spacer.

49. The process of claim 39, wherein the third primer comprises a blocked 3′

residue that is resistant to extension by DNA polymerase.

52. The process of claim 49, wherein the blocked 3′

residue comprises a dideoxy nucleotide.

53. The process of claim 39, wherein the fluorophore is attached to the third primer by a fluorophore-dT residue.

54. The process of claim 39, wherein the quencher is attached to the third primer by a quencher-dT residue.

55. The process of claim 39, wherein the fluorophore and quencher are separated by between 0 to 2 bases.

56. The process of claim 39, wherein the fluorophore and quencher are separated by between 0 to 5 bases.

57. The process of claim 39, wherein the fluorophore and quencher are separated by between 0 to 8 bases.

58. The process of claim 39, wherein the fluorophore and quencher are separated by between 0 to 10 bases.

59. The process of claim 39, wherein the fluorophore and quencher are separated by a greater distance when the extension blocked primer is unhybridized than when the extension blocked primer is hybridized to the target nucleic acid.

60. The process of claim 39, wherein the fluorophore or the quencher is attached to the noncomplementary or modified internal residue.

61. The process of claim 39, wherein the fluorophore comprises fluorescein, FAM, or TAMRA.

62. The process of claim 39, wherein the quencher comprises a non-fluorescent chromophore.

63. The process of claim 62, wherein the non-fluorescent chromophore is selected from the group consisting of DEEP DARK QUENCHER 1, DEEP DARK QUENCHER 2, BLACK HOLE QUENCHER 1, and BLACK HOLE QUENCHER 2.

64. The process of claim 39, wherein the first primer, second primer or third primer is 12 to 40 residues in length.

65. The process of claim 39, wherein the first primer, second primer or third primer is 12 to 60 residues in length.

66. The process of claim 39, wherein the process is performed in the presence of 1% to 12% polyethylene glycol.

67. The process of claim 39, wherein the process is performed in the presence of 6% to 8% polyethylene glycol.

68. The process of claim 39, wherein cleavage of the noncomplementary or modified internal residue forms a third 5′

primer double stranded structure and a 3′

extension blocked primer double stranded structure, and further comprising extending the 3′

end of the third 5′

primer with one or more polymerases and dNTP to generate a second double stranded amplified nucleic acid which comprises the first nucleic acid primer and the third 5′

primer.

69. The process of claim 39, wherein the dNTP comprise dUTP and wherein the process is performed in the presence of uracil glycosylase for a first period of less than 20 minutes and wherein the process is performed in the presence of uracil glycosylase inhibitor after the first period.