Dual resonance energy transfer nucleic acid probes

• US 20030129611A1
• Filed: 06/25/2002
• Published: 07/10/2003
• Est. Priority Date: 06/25/2001
• Status: Active Grant

• Current Assignee: Georgia Tech Research Corporation (University System of Georgia)
• Original Assignee: Georgia Tech Research Corporation (University System of Georgia)
• Inventors: Tsourkas, Andrew, Bao, Gang, Xu, Yangqing
• Granted Patent: US 7,081,336 B2
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: C12Q 1/6818 involving interaction of two or more labels, e.g. resonant energy transfer
• CPC Class Codes: C12Q 2525/301 Hairpin oligonucleotides
• CPC Class Codes: C12Q 2565/101 Interaction between at least two labels

Abstract

Dual nucleic acid probes with resonance energy transfer moieties are provided. In particular, fluorescent or luminescent resonance energy transfer moieties are provided on hairpin stem-loop molecular beacon probes that hybridize sufficiently near each other on a subject nucleic acid, e.g. mRNA, to generate an observable interaction. The invention also provides lanthanide chelate luminescent resonance energy transfer moieties on linear and stem-loop probes that hybridize sufficiently near each other on a subject nucleic acid to generate an observable interaction. The invention thereby provides detectable signals for rapid, specific and sensitive hybridization determination in vivo. The probes are used in methods of detection of nucleic acid target hybridization for the identification and quantification of tissue and cell-specific gene expression levels, including response to external stimuli, such as drug candidates, and genetic variations associated with disease, such as cancer.

Claims

1. A composition for detection of a subject nucleic acid comprising,

a. a first nucleic acid probe that hybridizes to a first nucleic acid target sequence on the subject nucleic acid, forms a stem-loop structure when not bound to the first nucleic acid target sequence, and incorporates a resonance energy transfer donor moiety;

and

b. a second nucleic acid probe that hybridizes to a second nucleic acid target sequence on the subject nucleic acid, forms a stem-loop structure when not bound to the second nucleic acid target sequence, and incorporates a resonance energy transfer acceptor moiety, wherein the first nucleic acid target sequence and the second nucleic acid target sequence are separated by a number of nucleotides on the subject nucleic acid such that a resonance energy transfer signal from interaction between the donor moiety of the first nucleic acid probe and the acceptor moiety of the second nucleic acid probe can be detected to determine hybridization of both the first nucleic acid probe and the second nucleic acid probe to the subject nucleic acid.

2. The composition of claim 1, wherein the first nucleic acid probe further incorporates a quencher moiety, such that an interaction between the donor moiety of the first nucleic acid probe and the quencher moiety can be detected to differentiate between the first nucleic acid probe in the stem-loop structure and non-stem-loop structure.

3. The composition of claim 1, wherein the second nucleic acid probe further incorporates a quencher moiety, such that an interaction between the acceptor moiety of the second nucleic acid probe and the quencher moiety can be detected to differentiate between the second nucleic acid probe in the stem-loop structure and non-stem-loop structure.

4. The composition of claim 1, wherein the first nucleic acid probe further incorporates a resonance energy transfer acceptor moiety, such that a resonance energy transfer signal from interaction between the donor moiety and the acceptor moiety on the first nucleic acid probe can be detected to differentiate between the first nucleic acid probe in the stem-loop structure and non-stem-loop structure.

5. The composition of claim 1, wherein the second nucleic acid probe further incorporates a resonance energy transfer donor moiety, such that a resonance energy transfer signal from interaction between the donor moiety and the acceptor moiety on the second nucleic acid probe can be detected to differentiate between the second nucleic acid probe in the stem-loop structure and non-stem-loop structure.

6. The composition of claim 1, wherein the resonance energy transfer signal is due to fluorescence resonance energy transfer.

7. The composition of claim 1, wherein the resonance energy transfer signal is due to fluorescence resonance energy transfer and the donor moiety is 6-Fam fluorophore.

8. The composition of claim 1, wherein the resonance energy transfer signal is due to fluorescence resonance energy transfer and the acceptor moiety is Cy-3, ROX or Texas Red.

9. The composition of claim 1, wherein the resonance energy transfer signal is due to luminescence resonance energy transfer.

10. The composition of claim 1, wherein the resonance energy transfer signal is due to luminescence resonance energy transfer and the donor moiety is a lanthanide chelator molecule.

11. The composition of claim 1, wherein the resonance energy transfer signal is due to luminescence resonance energy transfer and the donor moiety is Europium or Terbium.

12. The composition of claim 1, wherein the resonance energy transfer signal is due to luminescence resonance energy transfer and the donor moiety is a lanthanide chelator molecule selected from DTPA-cytosine, DTPA-cs124, BCPDA, BHHCT, Isocyanato-EDTA, Quantum Dye, or W1024.

13. The composition of claim 1, wherein the donor moiety is a lanthanide chelate and the acceptor moiety is an organic dye, Cy3, Cy5, ROX or Texas Red, or a phycobiliprotein.

14. The composition of claim 1, wherein the acceptor moiety is a phycobiliprotein selected from Red Phycoerythrin (RPE), Blue Phycoerythrin (BPE), or Allophycocyanin (APC).

15. The composition of claim 1, wherein the first or second nucleic acid probes comprises 5 to 50 nucleotides.

16. The composition of claim 1, wherein the first or second nucleic acid probes comprises 10 to 40 nucleotides.

17. The composition of claim 1, wherein the first or second nucleic acid probes comprises 15 to 30 nucleotides.

18. The composition of claim 1, wherein the first or second nucleic acid probes comprises 20 to 25 nucleotides.

19. The composition of claim 1, wherein the first or second nucleic acid probes comprises a 2′

-O-methyl nucleotide backbone.

20. The composition of claim 1, wherein one end of the first or second nucleic acid probes participates in both stem-loop formation and hybridization to the nucleic acid target sequence.

21. The composition of claim 1, wherein the first nucleic acid target sequence and the second nucleic acid target sequence are separated by 1 to 20 nucleotides.

22. The composition of claim 1, wherein the first nucleic acid target sequence and the second nucleic acid target sequence are separated by 2 to 10 nucleotides.

23. The composition of claim 1, wherein the first nucleic acid target sequence and the second nucleic acid target sequence are separated by 3 to 7 nucleotides.

43. A method of detecting a subject nucleic acid, comprising combining the composition of claim 1 or claim 24 with a sample suspected of containing the subject nucleic acid, and detecting hybridization by resonance energy transfer signals to determine the presence or absence of the subject nucleic acid in the sample.

44. The method of claim 43, wherein the method is performed in vivo.

45. The method of claim 44, wherein the sample contains a living cell.

46. The method of claim 43, wherein the subject nucleic acid comprises a genetic point mutation, deletion or insertion relative to a control nucleic acid.

47. The method of claim 43, wherein the detection of the subject nucleic acid indicates the presence of a cancer in the sample.

48. The method of claim 43, wherein the subject nucleic acid comprises K-ras, survivin, p53, p16, DPC4, or BRCA2.

49. The method of claim 43, wherein the detection of the subject nucleic acid indicates an alteration of the expression pattern of the subject nucleic acid in response to an external stimulus.

50. The method of claim 43, wherein the detection is performed with single- or multiple-photon microscopy, time-resolved fluorescence microscopy or fluorescence endoscopy.

24. A composition for detection of a subject nucleic acid comprising,

a. a first nucleic acid probe that hybridizes to a first nucleic acid target sequence on the subject nucleic acid, and incorporates a luminescence resonance energy transfer lanthanide chelate donor moiety;

and

b. a second nucleic acid probe that hybridizes to a second nucleic acid target sequence on the subject nucleic acid, and incorporates an organic resonance energy transfer acceptor moiety, wherein the first nucleic acid target sequence and the second nucleic acid target sequence are separated by a number of nucleotides on the subject nucleic acid such that a luminescence resonance energy transfer signal from interaction between the lanthanide chelate donor moiety of the first nucleic acid probe and the acceptor moiety of the second nucleic acid probe can be detected to determine hybridization of both the first nucleic acid probe and the second nucleic acid probe to the subject nucleic acid.

25. The composition of claim 24, wherein the first nucleic acid probe or second nucleic acid probe is linear or randomly coiled when not hybridized to the first or second nucleic acid target sequences, respectively.

26. The composition of claim 24, wherein the first nucleic acid probe or second nucleic acid probe forms a stem-loop structure when not hybridized to the first or second nucleic acid target sequences, respectively.

27. The composition of claim 26, wherein the first nucleic acid probe further incorporates a quencher moiety, such that an interaction between the donor moiety of the first nucleic acid probe and the quencher moiety can be detected to differentiate between the first nucleic acid probe in the stem-loop structure and non-stem-loop structure.

28. The composition of claim 26, wherein the second nucleic acid probe further incorporates a quencher moiety, such that an interaction between the acceptor moiety of the second nucleic acid probe and the quencher moiety can be detected to differentiate between the second nucleic acid probe in the stem-loop structure and non-stem-loop structure.

29. The composition of claim 24, wherein the lanthanide donor moiety is Europium or Terbium.

30. The composition of claim 24, wherein the donor moiety is selected from a lanthanide chelate DTPA-cytosine, DTPA-cs124, BCPDA, BHHCT, Isocyanato-EDTA, Quantum Dye, or W1024.

31. The composition of claim 24, wherein the donor moiety is a lanthanide chelate and the acceptor moiety is an organic dye or a phycobiliprotein.

32. The composition of claim 24, wherein the acceptor moiety is a phycobiliprotein selected from Red Phycoerythrin (RPE), Blue Phycoerythrin (BPE), or Allophycocyanin (APC).

33. The composition of claim 24, wherein the second nucleic acid probe comprises a plurality of acceptor moieties.

34. The composition of claim 24, wherein the first or second nucleic acid probes comprises 5 to 50 nucleotides.

35. The composition of claim 24, wherein the first or second nucleic acid probes comprises 10 to 40 nucleotides.

36. The composition of claim 24, wherein the first or second nucleic acid probes comprises 15 to 30 nucleotides.

37. The composition of claim 24, wherein the first or second nucleic acid probes comprises 20 to 25 nucleotides.

38. The composition of claim 24, wherein the nucleic acid probes comprises a 2′

-O-methyl nucleotide backbone.

39. The composition of claim 24, wherein one end of either the first or the second nucleic acid probes participates in both stem-loop formation and hybridization to the target sequence nucleic acid.

40. The composition of claim 24, wherein the first nucleic acid target sequence and the second nucleic acid target sequence are separated by 1 to 20 nucleotides.

41. The composition of claim 24, wherein the first nucleic acid target sequence and the second nucleic acid target sequence are separated by 2 to 10 nucleotides.

42. The composition of claim 24, wherein the first nucleic acid target sequence and the second nucleic acid target sequence are separated by 3 to 7 nucleotides.