THERMOPHILIC HELICASE DEPENDENT AMPLIFICATION TECHNOLOGY WITH ENDPOINT HOMOGENOUS FLUORESCENT DETECTION

• US 20100285473A1
• Filed: 01/27/2010
• Published: 11/11/2010
• Est. Priority Date: 01/27/2009
• Status: Abandoned Application

• Current Assignee: Dirk Loeffert, Gwynne Roth, Irina Nazarenko, John Wolff, Thomas Forbes, Victoria Doseeva
• Original Assignee: Dirk Loeffert, Gwynne Roth, Irina Nazarenko, John Wolff, Thomas Forbes, Victoria Doseeva
• Inventors: Doseeva, Victoria, Roth, Gwynne, Wolff, John, Forbes, Thomas, Nazarenko, Irina, Loeffert, Dirk
• Application Number:
  US12/695,001
• Publication Number:
  US 20100285473A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: C12Q 1/6844 Nucleic acid amplification reactions
• CPC Class Codes: C12Q 1/686 Polymerase chain reaction [PCR]
• CPC Class Codes: C12Q 1/6865 Promoter-based amplification, e.g. nucleic acid sequence amplification [NASBA], self-sustained sequence replication [3SR] or transcription-based amplification system [TAS]
• CPC Class Codes: C12Q 2521/513 Winding/unwinding enzyme, e.g. helicase
• CPC Class Codes: C12Q 2527/137 Concentration of a component of medium
• CPC Class Codes: C12Q 2563/131 the label being a member of a cognate binding pair, i.e. extends to antibodies, haptens, avidin

Abstract

Disclosed herein are methods of amplifying a target nucleic acid in a helicase-dependent reaction. Also disclosed are methods of amplifying and detecting a target nucleic acid in a helicase-dependent reaction as well as modified detection labels to assist in the detection.

Claims

1. A method of amplifying a double stranded target nucleic acid in a helicase-dependent reaction, comprising:

(a) denaturing the target nucleic acid;

(b) contacting one or more oligonucleotide probes with the denatured target nucleic acid, wherein one or more of the oligonucleotide probes hybridize to the denatured target nucleic acid to form double-stranded probe-target hybrids;

(c) contacting the double-stranded probe-target hybrids with one or more capture antibodies wherein the one or more capture antibodies hybridize to the double-stranded probe-target hybrids to form captured double-stranded probe-target hybrids,

(d) removing all uncaptured nucleic acids;

(e) adding one or more oligonuceotide primers, wherein the oligonucleotide primers hybridize to the target nucleic acid;

(f) synthesizing an extension product of the oligonucleotide primers which is complementary to the target nucleic acid, by means of a DNA polymerase to form a target nucleic acid duplex;

(g) contacting the target nucleic acid duplex of step (f) with a helicase preparation and amplifying the target nucleic acid duplex in a helicase-dependent reaction.

2. The method of claim 1, wherein steps (e), (f) and (g) are carried out simultaneously.

3. The method of claim 1, wherein steps (f) and (g) are carried out simultaneously.

4. The method of claim 1, wherein the double stranded target nucleic acid is in a target nucleic acid sample.

5. The method of claim 4, wherein the sample is a blood, urine, stool, saliva, tear, bile cervical, urogenital, nasal swabs, sputum, or other biological sample.

6. The method of claim 1, wherein the double stranded target nucleic acid is isolated from a sample prior to step (a).

7. The method of claim 1, wherein amplification is isothermal.

8. The method of claim 1, wherein the polynucleotide probes are RNA.

9. The method of claim 1, wherein the helicase preparation comprises a helicase and optionally a single strand binding protein.

10. The method of claim 1, wherein the helicase preparation comprises a helicase and a single strand binding protein (SSB) unless the helicase preparation comprises a thermostable helicase wherein the single strand binding protein is optional.

11. The method of claim 1, wherein the amplification does not occur in the absence of a helicase as determined by gel electrophoresis.

12. The method of claim 1, wherein steps (e) through (g) are conducted in a homogenous assay.

13. The method of claim 1, wherein step (a) further comprises heating the target nucleic acid to denature the target nucleic acid.

14. The method of claim 11, wherein step (a) further comprises incubating the target nucleic acid in the presence of NaOH prior to step (b) as step (a).

15. The method of claim 11, wherein step (a) further comprises incubating the target nucleic acid at 65°

C. for 10 minutes in the presence of 50 mM NaOH prior to step (b).

16. The method of claim 1, wherein helicase preparation comprises an additive.

17. The method of claim 16, wherein the additive is selected from the group consisting of sugars, chaperones, proteins, saccharides, amino acids, polyalcohols, and their derivatives, other osmolytes, amino acid derivatives, and chaperone proteins.

18. The method of claim 16, wherein the additive is selected from the group consisting of DMSO, betaine, sorbitol, dextran sulfate and mixtures thereof.

19. The method of claim 18, wherein DMSO is used at a final concentration of between 1 and 2%

20. The method of claim 18, wherein betaine is used at a final concentration of 0.1M-0.5M.

21. The method of claim 18, wherein sorbitol is used at a final concentration of 0.1M-0.3M.

22. The method of claim 18, wherein dextran sulfate is used at a final concentration of 10 pM-1 nM.

23. The method of claim 1, wherein the hybrid capture antibodies comprise a magnetic bead.

24. The method of claim 1, wherein one or more of the oligonucleotide primers are present in different concentrations.

25. The method of claim 1, further comprising detecting the target nucleic acid.

26. The method of claim 1, wherein the method comprises adding a detection label.

27. The method of claim 26, wherein the detection label is added during or after step (e), (f) or (g).

28. The method of claim 25, wherein the target nucleic acid is detected both during and after the amplification reaction.

29. The method of claim 25, wherein the target nucleic acid is detected during the amplification reaction.

30. The method of claim 25, wherein the target nucleic acid is detected after the amplification reaction.

31. The method of claim 25, wherein steps (e) through (g) and the detection are carried out in a homogenous assay.

32. The method of claim 25, wherein the target nucleic acid is detected by end point fluorescent detection.

33. The method of claim 26, wherein the detection label is a modified TaqMan probe.

34. The method of claim 33, wherein the modified TaqMan probe has a short tail at 3′

-end of the modified TaqMan probe complementary to the 5′

-end modified TaqMan probe.

35. The method of claim 34, wherein the short tail of the modified TaqMan probe is not complementary to the target.

36. The method of claim 34, wherein the short tail of the modified TaqMan probe is also complementary to the target.

37. The method of claim 33, wherein the modified TaqMan probe has a short tail at 5′

-end of the modified TaqMan probe complementary to the 3′

-end modified TaqMan probe.

38. The method of claim 37, wherein the short tail of the modified TaqMan probe is not complementary to the target.

39. The method of claim 37, wherein the short tail of the modified TaqMan probe is also complementary to the target.

40. A method of amplifying a single stranded target nucleic acid in a helicase-dependent reaction, comprising:

(a) contacting one or more oligonucleotide probes with the single stranded target nucleic acid, wherein one or more of the oligonucleotide probes hybridize to the target nucleic acid to form double-stranded probe-target hybrids;

(b) contacting the double-stranded probe-target hybrids with one or more capture antibodies, wherein the one or more of capture antibodies hybridize to the double-stranded probe-target hybrids to form captured double-stranded probe-target hybrids,

(c) removing all uncaptured nucleic acids;

(d) adding one or more oligonuceotide primers, wherein the oligonucleotide primers hybridize to the target nucleic acid;

(e) synthesizing an extension product of the oligonucleotide primers which is complementary to the target nucleic acid, by means of a DNA polymerase to form a target nucleic acid duplex;

(f) contacting the target nucleic acid duplex of step (e) with a helicase preparation and amplifying the target nucleic acid duplex in a helicase-dependent reaction.

41. The method of claim 40, wherein the single stranded target nucleic acid is DNA.

42. The method of claim 40, wherein the single stranded target nucleic acid is cDNA and wherein the cDNA is produced from reverse transcribing a target mRNA.

43. The method of claim 40, wherein steps (e), (f) and (g) are carried out simultaneously.

44. The method of claim 40, wherein steps (f) and (g) are carried out simultaneously.

45. The method of claim 40, wherein the single stranded target nucleic acid is in a target nucleic acid sample.

46. The method of claim 45, wherein the sample is a blood, urine, stool, saliva, tear, bile cervical, urogenital, nasal swabs, sputum, or other biological sample.

47. The method of claim 40, wherein amplification is isothermal.

48. The method of claim 41, wherein the polynucleotide probes are RNA.

49. The method of claim 40, wherein one or more of the oligonucleotide primers are present in different concentrations.

50. The method of claim 40, wherein the helicase preparation comprises a helicase and optionally a single strand binding protein.

51. The method of claim 40, wherein the helicase preparation comprises a helicase and a single strand binding protein (SSB) unless the helicase preparation comprises a thermostable helicase wherein the single strand binding protein is optional.

52. The method of claim 40, wherein the amplification does not occur in the absence of a helicase as determined by gel electrophoresis.

53. The method of claim 40, wherein steps (e) through (g) are conducted in a homogenous assay.

54. The method of claim 40, wherein helicase preparation comprises an additive.

55. The method of claim 54, wherein the additive is selected from the group consisting of sugars, chaperones, proteins, saccharides, amino acids, polyalcohols, and their derivatives, other osmolytes, amino acid derivatives, and chaperone proteins.

56. The method of claim 54, wherein the additive is selected from the group consisting of DMSO, betaine, sorbitol, dextran sulfate and mixtures thereof.

57. The method of claim 56, wherein DMSO is used at a final concentration of between 1 and 2%

58. The method of claim 56, wherein betaine is used at a final concentration of 0.1M-0.5M.

59. The method of claim 56, wherein sorbitol is used at a final concentration of 0.1M-0.3M.

60. The method of claim 56, wherein dextran sulfate is used at a final concentration of 10 pM-1 nM.

61. The method of claim 40, wherein the hybrid capture antibodies comprise a magnetic bead.

62. The method of claim 40, further comprising detecting the target nucleic acid.

63. The method of claim 62, wherein steps (e) through (g) and the detection are carried out in a homogenous assay.

64. The method of claim 40, wherein the method comprises adding a detection label.

65. The method of claim 64, wherein the detection label is added during or after step (e), (f) or (g).

66. The method of claim 62, wherein the target nucleic acid is detected both during and after the amplification reaction.

67. The method of claim 62, wherein the target nucleic acid is detected during the amplification reaction.

68. The method of claim 62, wherein the target nucleic acid is detected after the amplification reaction.

69. The method of claim 68, wherein the target nucleic acid is detected by end point fluorescent detection.

70. The method of claim 64, wherein the detection label is a modified TaqMan probe.

71. The method of claim 70, wherein the modified TaqMan probe has a short tail at 3′

-end of the modified TaqMan probe complementary to the 5′

-end modified TaqMan probe.

72. The method of claim 70, wherein the modified TaqMan probe has a short tail at 5′

-end of the modified TaqMan probe complementary to the 3′

-end modified TaqMan probe.

73. The method of claim 71, wherein the short tail of the modified TaqMan probe is not complementary to the target.

74. The method of claim 72, wherein the short tail of the modified TaqMan probe is not complementary to the target.

75. The method of claim 71, wherein the short tail of the modified TaqMan probe is also complementary to the target.

76. The method of claim 72, wherein the short tail of the modified TaqMan probe is also complementary to the target.

77. The method of claim 40, wherein the single stranded target nucleic acid is RNA.

78. The method of claim 77, wherein the one or more oligonucleotide probes are DNA probes.

79. A method of amplifying two double stranded target nucleic acids in a single helicase-dependent reaction, wherein the two double stranded target nucleic acids comprise a first and a second double stranded target nucleic acids comprising:

(a) denaturing the target nucleic acids;

(b) contacting the first denatured target nucleic acid with one or more oligonucleotide probes wherein the oligonucleotide probes hybridize to the first denatured target nucleic acid to form first target double-stranded probe-target hybrids, and contacting the second denatured target nucleic acid with one or more oligonucleotide probes wherein the oligonucleotide probes hybridize to the second denatured target nucleic acid to form second target double-stranded probe-target hybrids;

(c) contacting the first and second double-stranded probe-target hybrids with one or more capture antibodies, wherein the one or more capture antibodies bind to the first and second double-stranded probe-target hybrids to form captured first and second double-stranded probe-target hybrids,

(d) removing all uncaptured nucleic acids;

(e) adding one or more first target oligonuceotide primers, wherein the first target oligonucleotide primers hybridize to the first target nucleic acid and adding one or more second target oligonuceotide primers, wherein the second target oligonucleotide primers hybridize to the second target nucleic acid;

(f) synthesizing extension products of the first and second target oligonucleotide primers which are complementary to the first and second target nucleic acids, respectively, by means of a DNA polymerase to form first and second target nucleic acid duplexes;

(g) contacting the first and second target nucleic acid duplexes of step (f) with a helicase preparation and amplifying the target nucleic acid duplexes in a helicase-dependent reaction, wherein the helicase preparation comprises one or more primers that hybridize to the first target nucleic acid and further comprises one or more primers that hybridize to the second target nucleic acid.