Detection of nucleic acids by fluorescence quenching

• US 5,928,869 A
• Filed: 05/30/1997
• Issued: 07/27/1999
• Est. Priority Date: 05/30/1997
• Status: Expired due to Fees

• Current Assignee: Becton, Dickinson & Co
• Original Assignee: Becton, Dickinson & Co
• Inventors: Pitner, J. Bruce, Schram, James L., Nadeau, James G., Linn, C. Preston
• Primary Examiner(s): LeGuyader, John L.
• Assistant Examiner(s): SHIBUYA, MARK LANCE
• Application Number:
  US08/865,675
• Time in Patent Office: 788 Days
• Field of Search: 435/6, 435/91.2, 536/23.1, 536/24.3, 536/24.33, 536/25.32, 536/25.3
• US Class Current: 435/6.18
• CPC Class Codes: C12Q 1/6818 involving interaction of two or more labels, e.g. resonant energy transfer
• CPC Class Codes: C12Q 1/6827 for detection of mutation or polymorphism
• CPC Class Codes: C12Q 1/6858 Allele-specific amplification
• CPC Class Codes: C12Q 2521/301 Endonuclease
• CPC Class Codes: C12Q 2525/301 Hairpin oligonucleotides
• CPC Class Codes: C12Q 2533/101 Primer extension
• CPC Class Codes: C12Q 2565/1015 labels being on the same oligonucleotide

Abstract

A detector oligonucleotide having a sequence which forms an intramolecularly base-paired secondary structure is described for use in detecting nucleic acid target sequences and target sequence amplification. The detector oligonucleotide is further modified by linkage to two dyes which form a donor/acceptor dye pair. The two dyes are positioned on the detector oligonucleotide such that they are in close spatial proximity in the base-paired, folded secondary structure, thereby causing quenching of donor fluorescence. The detector oligonucleotide may optionally further comprise a restriction endonuclease recognition site (RERS) which remains partially or entirely single-stranded in the base-paired secondary structure. The RERS is flanked by the two dyes. In the presence of target, the base-paired secondary structure is unfolded or linearized, increasing the distance between the donor and acceptor dyes and causing a change in fluorescence of the donor and/or the acceptor. If an RERS is present, it is rendered double-stranded in the presence of target, allowing cleavage or nicking by a restriction endonuclease and separation of the two dyes onto separate nucleic acid fragments. This may further contribute to the magnitude of the change in fluorescence.

Claims

1. A method for detecting the presence of a nucleic acid target sequence comprising:

a) hybridizing to the target sequence a detector oligonucleotide comprising a single-stranded target binding sequence and an intramolecularly base-paired secondary structure 5'"'"' to the target binding sequence, wherein at least a portion of the target binding sequence forms a single-stranded tail which binds to the target sequence, the secondary structure having linked thereto a donor fluorophore and an acceptor dye such that fluorescence of the donor fluorophore is quenched;

b) in a primer extension reaction, synthesizing a complementary strand using the base-paired secondary structure as a template, thereby linearizing or unfolding the base-paired secondary structure and producing a change in a fluorescence parameter, and;

c) detecting the change in the fluorescence parameter as an indication of the presence of the target sequence.

2. The method of claim 1 wherein the base-paired secondary structure is selected from the group consisting of stem-loop structures, pseudoknots and triple helices.

3. The method of claim 1 wherein the complementary strand is synthesized in a target amplification reaction.

4. The method of claim 1 wherein the complementary strand is synthesized by extension of the target sequence using the detector oligonucleotide as a template.

5. The method of claim 1 wherein the base-paired secondary structure comprises a totally or partially single-stranded restriction endonuclease recognition site.

6. The method of claim 1 wherein a change in fluorescence intensity is detected as an indication of the presence of the target sequence.

7. The method of claim 6 wherein an increase in donor fluorescence intensity or a decrease in acceptor fluorescence intensity is detected as an indication of the presence of the target sequence.

8. The method of claim 6 wherein the change in fluorescence intensity is detected as a) an increase in a ratio of donor fluorophore fluorescence after linearizing or unfolding to donor fluorophore fluorescence in the detector oligonucleotide prior to linearizing or unfolding, or b) as a decrease in a ratio of acceptor dye fluorescence after linearizing or unfolding to acceptor dye fluorescence in the detector oligonucleotide prior to linearizing or unfolding.

9. The method of claim 1 wherein a change in fluorescence lifetime is detected as an indication of the presence of the target sequence.

10. The method of claim 1 wherein the change in the fluorescence parameter is detected in real-time.

11. The method of claim 1 wherein the change in the fluorescence parameter is detected at an endpoint.

12. The method of claim 1 wherein the donor fluorophore and the acceptor dye are separated by about 7-75 nucleotides in the linearized or unfolded secondary structure.

13. The method of claim 1 wherein the secondary structure is a hairpin.

14. The method of claim 1 wherein the donor fluorophore is fluorescein and the acceptor dye is Rhodamine X or the donor fluorophore is Rhodamine X and the acceptor dye is Cy5.

15. The method of claim 1 wherein the intramolecularly base-paired secondary structure comprises a portion of the target binding sequence.

48. The method of claim 3 wherein the detector oligonucleotide is an amplification primer.

49. The method of claim 48 wherein the amplification primer is an amplification primer for use in PCR, SDA, NASBA, TMA or 3SR.

50. The method of claim 3 wherein the detector oligonucleotide is a signal primer.

51. The method of claim 3 wherein the target amplification reaction is selected from the group consisting of PCR, NASBA, 3SR, TMA and SDA.

52. The method of claim 1 further comprising quantitating an amount of the target sequence initially present.

53. The method of claim 52 wherein the amount of the target sequence is quantitated by a rate of change in the fluorescence parameter.

54. The method of claim 52 wherein the amount of the target sequence is quantitated by monitoring time to positivity.

55. The method of claim 5 wherein the restriction endonuclease recognition site is rendered double-stranded by the primer extension reaction and the double-stranded restriction endonuclease recognition site is cleaved or nicked by a restriction endonuclease.

16. A method for detecting amplification of a target sequence comprising, in an amplification reaction:

a) hybridizing to the target sequence a detector oligonucleotide comprising a single-stranded target binding sequence and an intramolecularly base-paired secondary structure 5'"'"' to the target binding sequence, wherein at least a portion of the target binding sequence forms a single-stranded tail which binds to the target sequence, the secondary structure having linked thereto a donor fluorophore and an acceptor dye such that fluorescence of the donor fluorophore is quenched;

b) extending the hybridized detector oligonucleotide on the target sequence with a polymerase to produce a detector oligonucleotide extension product and separating the detector oligonucleotide extension product from the target sequence;

c) hybridizing a primer to the detector oligonucleotide extension product and extending the primer with the polymerase, thereby linearizing or unfolding the secondary structure and producing a change in a fluorescence parameter, and;

d) detecting the change in the fluorescence parameter as an indication of amplification of the target sequence.

17. The method of claim 16 wherein the target sequence is amplified by Strand Displacement Amplification.

18. The method of claim 16 wherein the secondary structure further comprises a partially or entirely single-stranded restriction endonuclease recognition site.

19. The method of claim 18 wherein the restriction endonuclease recognition site is for BsoBI or AvaI.

20. The method of claim 16 wherein the target sequence is amplified by the Polymerase Chain Reaction.

21. The method of claim 16 wherein the target sequence is amplified by 3SR, TMA or NASBA.

22. The method of claim 16 wherein a change in fluorescence intensity is detected.

23. The method of claim 22 wherein an increase in donor fluorophore fluorescence intensity or a decrease in acceptor dye fluorescence intensity is detected as an indication of amplification of the target sequence.

24. The method of claim 22 wherein the change in fluorescence intensity is detected as a) an increase in a ratio of donor fluorophore fluorescence after linearizing or unfolding and donor fluorophore fluorescence in the detector oligonucleotide prior to linearizing or unfolding, or b) as a decrease in a ratio of acceptor dye fluorescence after linearizing or unfolding and acceptor dye fluorescence in the detector oligonucleotide prior to linearizing or unfolding.

25. The method of claim 22 wherein the change in fluorescence intensity is detected in real-time.

26. The method of claim 22 wherein the change in fluorescence intensity is detected at a selected end-point in the amplification reaction.

27. The method of claim 16 wherein the donor fluorophore and the acceptor dye are separated by about 7-75 nucleotides in the linearized or unfolded secondary structure.

28. The method of claim 16 wherein the donor fluorophore is fluorescein and the acceptor dye is Rhodamine X or the donor fluorophore is Rhodamine X and the acceptor dye is Cy5.

29. The method of claim 16 wherein the intramolecularly base-paired secondary structure comprises a portion of the target binding sequence.

56. The method of claim 16 wherein the detector oligonucleotide is an amplification primer.

57. The method of claim 16 wherein the detector oligonucleotide is a signal primer.

58. The method of claim 16 further comprising quantitating an amount of the target sequence initially present.

59. The method of claim 58 wherein the amount of the target sequence is quantitated by a rate of change in the fluorescence parameter.

60. The method of claim 58 wherein the amount of the target sequence is quantitated by monitoring time to positivity.

61. The method of claim 16 wherein the secondary structure is a hairpin.

62. The method of claim 18 wherein the restriction endonuclease recognition site is rendered double-stranded by extension of the primer and the double-stranded restriction endonuclease recognition site is cleaved or nicked by a restriction endonuclease.

30. A method for detecting a target sequence comprising:

a) providing a detector oligonucleotide comprising a single-stranded target binding sequence and an intramolecularly base-paired secondary structure adjacent to the target binding sequence, wherein at least a portion of the target binding sequence forms a single-stranded 5'"'"' or 3'"'"' tail which binds to the target sequence, the secondary structure having linked thereto a donor fluorophore and an acceptor dye such that fluorescence of the donor fluorophore is quenched;

b) hybridizing the detector oligonucleotide to the target sequence, thereby reducing donor fluorophore quenching and producing a change in a fluorescence parameter, and;

c) detecting the change in the fluorescence parameter as an indication of the presence of the target sequence.

31. The method of claim 30 wherein the secondary structure comprises a portion of the target binding sequence.

32. The method of claim 30 wherein the intramolecularly base-paired secondary structure is 5'"'"' to the target binding sequence.

33. The method of claim 30 wherein the intramolecularly base-paired secondary structure is 3'"'"' to the target binding sequence.

34. The method of claim 30 wherein the change in the fluorescence parameter is detected in real-time.

35. The method of claim 30 wherein the change in the fluorescence parameter is detected at an endpoint.

36. The method of claim 30 wherein the change in the fluorescence parameter is a change in fluorescence intensity.

37. The method of claim 30 wherein the secondary structure is a hairpin.

38. The method of claim 30 wherein the detector oligonucleotide is immobilized on a solid phase.

63. The method of claim 31 wherein the detector oligonucleotide hybridizes to the target sequence with at least one mismatch, thereby reducing the change in the fluorescence parameter as compared to hybridization of the detector oligonucleotide without the mismatch.

64. The method of claim 30 further comprising quantitating an amount of the target sequence initially present.

65. The method of claim 64 wherein the amount of the target sequence is quantitated by a rate of change in the fluorescence parameter.

66. The method of claim 64 wherein the amount of the target sequence is quantitated by monitoring time to positivity.

67. The method of claim 30 wherein the secondary structure further comprises a totally or partially single-stranded restriction endonuclease recognition site.

68. The method of claim 67 wherein the restriction endonuclease recognition site is rendered double-stranded by hybridizing to the target sequence and the double-stranded restriction endonuclease recognition site is cleaved or nicked by a restriction endonuclease.

39. An oligonucleotide comprising a single-stranded target binding sequence and an intramolecularly base-paired secondary structure adjacent to the target binding sequence, wherein at least a portion of the target binding sequence forms a single-stranded 5'"'"' or 3'"'"' tail which binds to a target sequence, the secondary structure having linked thereto a first dye and a second dye such that fluorescence of the first or the second dye is quenched in the intramolecularly base-paired secondary structure and a change in a fluorescence parameter is detectable upon linearization or unfolding of the secondary structure.

40. The oligonucleotide of claim 39 wherein the secondary structure comprises a partially or entirely single-stranded restriction endonuclease recognition site.

41. The oligonucleotide of claim 39 wherein the intramolecularly base-paired secondary structure is 5'"'"' to the target binding sequence.

42. The oligonucleotide of claim 41 wherein the intramolecularly base-paired secondary structure comprises a portion of the target binding sequence.

43. The oligonucleotide of claim 39 wherein the intramolecularly base-paired secondary structure is 3'"'"' to the target binding sequence.

44. The oligonucleotide of claim 43 wherein the intramolecularly base-paired secondary structure comprises a portion of the target binding sequence.

45. The oligonucleotide of claim 39 wherein the first dye is Cy5 or fluorescein and the second dye is Rhodamine X.

46. The oligonucleotide of claim 39 wherein the first dye is fluorescein and the second dye is Dabcyl.

47. The oligonucleotide of claim 39 which is immobilized on a solid phase.

69. A method for detecting a nucleic acid target sequence comprising:

a) hybridizing to the target sequence a detector oligonucleotide comprising a single-stranded target binding sequence and an intramolecularly base-paired secondary structure 5'"'"' to the target binding sequence, wherein at least a portion of the target binding sequence forms a single-stranded tail which binds to the target sequence and the intramolecularly base-paired secondary structure comprises a partially or entirely single-stranded restriction endonuclease recognition site, the secondary structure having linked thereto a donor fluorophore and an acceptor dye such that fluorescence of the donor fluorophore is quenched;

b) in a primer extension reaction, synthesizing a complementary strand using the base-paired secondary structure as a template, thereby linearizing or unfolding the base-paired secondary structure, rendering the restriction endonuclease recognition site partially or entirely double-stranded and producing a change in a fluorescence parameter;

c) optionally, cleaving or nicking the partially or entirely double-stranded restriction endonuclease recognition site, and;

d) detecting the change in the fluorescence parameter as an indication of the presence of the target sequence.

70. The method of claim 69 wherein the complementary strand is synthesized in a target amplification reaction.

71. The method of claim 69 wherein a change in fluorescence intensity is detected as an indication of the presence of the target sequence.

72. A method for detecting amplification of a target sequence comprising, in an amplification reaction:

a) hybridizing to the target sequence a detector oligonucleotide comprising a single-stranded target binding sequence and an intramolecularly base-paired secondary structure 5'"'"' to the target binding sequence, wherein at least a portion of the target binding sequence forms a single-stranded tail which binds to the target sequence and the intramolecularly base-paired secondary structure comprises a partially or entirely single-stranded restriction endonuclease recognition site, the secondary structure having linked thereto a donor fluorophore and an acceptor dye such that fluorescence of the donor fluorophore is quenched;

b) extending the hybridized detector oligonucleotide on the target sequence with a polymerase to produce a detector oligonucleotide extension product and separating the detector oligonucleotide extension product from the target sequence;

c) hybridizing a primer to the detector oligonucleotide extension product and extending the primer with a polymerase, thereby linearizing or unfolding the secondary structure, rendering the restriction endonuclease recognition site partially or entirely double-stranded and producing a change in a fluorescence parameter;

d) optionally, cleaving or nicking the partially or entirely double-stranded restriction endonuclease recognition site, and;

e) detecting the change in the fluorescence parameter as an indication of the presence of the target sequence.

73. The method of claim 72 wherein the amplification reaction is SDA, PCR, 3SR, TMA or NASBA.

74. The method of claim 72 wherein a change in fluorescence intensity is detected.