Methods and compositions for detection and analysis of polynucleotides using light harvesting multichromophores

• US 7,270,956 B2
• Filed: 08/26/2003
• Issued: 09/18/2007
• Est. Priority Date: 08/26/2002
• Status: Active Grant

• Current Assignee: Regents of the University of California (University of California)
• Original Assignee: Regents of the University of California (University of California)
• Inventors: Bazan, Guillermo C., Wang, Shu, Gaylord, Brent S.
• Primary Examiner(s): Riley; Jezia
• Application Number:
  US10/648,945
• Publication Number:
  US 20040142344A1
• Time in Patent Office: 1,484 Days
• Field of Search: 435/6, 536/23.1, 536/26.6, 536/22.1, 536/24.3
• US Class Current: 435/6.19
• CPC Class Codes: C12Q 1/6813 Hybridisation assays
• CPC Class Codes: C12Q 1/6818 involving interaction of two or more labels, e.g. resonant energy transfer
• CPC Class Codes: C12Q 1/6825 Nucleic acid detection involving sensors
• CPC Class Codes: C12Q 1/6834 Enzymatic or biochemical coupling of nucleic acids to a solid phase
• CPC Class Codes: C12Q 2523/313 Irradiation, e.g. UV irradiation
• CPC Class Codes: C12Q 2563/107 fluorescence
• CPC Class Codes: C12Q 2565/107 Alteration in the property of hybridised versus free label oligonucleotides
• CPC Class Codes: Y10T 436/143333 Saccharide [e.g., DNA, etc.]

Abstract

Methods, compositions and articles of manufacture for assaying a sample for a target polynucleotide are provided. A sample suspected of containing the target polynucleotide is contacted with a polycationic multichromophore and a sensor polynucleotide complementary to the target polynucleotide. The sensor polynucleotide comprises a signaling chromophore to receive energy from the excited multichromophore and increase emission in the presence of the target polynucleotide. The methods can be used in multiplex form. Kits comprising reagents for performing such methods are also provided.

Claims

1. An assay method comprising:

providing a sample that is suspected of containing a target polynucleotide;

providing a polycationic multichromophore that upon excitation is capable of transferring energy to a signaling chromophore;

providing an anionic sensor polynucleotide that is complementary to the target polynucleotide, said sensor polynucleotide conjugated to the signaling chromophore, wherein said sensor polynucleotide can interact with the multichromophore and emitted light can be produced from the signaling chromophore upon excitation of the multichromophore, and wherein a greater amount of emitted light is produced from the signaling chromophore upon excitation of the multichromophore in the presence of target polynucleotide as compared to in the presence of a noncomplementary polynucleotide;

contacting the sample with the sensor polynucleotide and the multichromophore in a solution under conditions in which the sensor polynucleotide can hybridize to the target polynucleotide, if present;

exciting the multichromophore with a light source; and

detecting if light is emitted from the signaling chromophore.

2. The method of claim 1, wherein the multichromophore comprises a structure that is selected from the group consisting of a saturated polymer, a conjugated polymer, an aggregate of conjugated molecules, a dendrimer, and a semiconductor nanocrystal.

3. The method of claim 2, wherein the multichromophore comprises a saturated polymer.

4. The method of claim 2, wherein the multichromophore comprises a dendrimer.

5. The method of claim 2, wherein the multichromophore comprises a semiconductor nanocrystal.

6. The method of claim 2, wherein the multichromophore comprises a conjugated molecule.

7. The method of claim 6, wherein the conjugated polymer has the structure

8. The method of claim 2, wherein the multichromophore is an aggregate of conjugated molecules.

9. The method of claim 8, wherein the aggregate comprises molecules having the structure

10. The method of claim 1, wherein the sample is contacted with the sensor polynucleotide and the multichromophore in the presence of a sufficient amount of an organic solvent to decrease hydrophobic interactions between the sensor polynucleotide and the multichromophore.

11. The method of claim 1, wherein the sample is contacted with a plurality of different sensor polynucleotides having corresponding different sequences, each of said different sensor polynucleotides comprising a corresponding different signaling chromophore, wherein each of said different sensor polynucleotides can selectively hybridize to a corresponding different target polynucleotide.

12. The method of claim 1, wherein the signaling chromophore is a fluorophore.

13. The method of claim 12, wherein the fluorophore is selected from a semiconductor nanocrystal, a fluorescent dye, and a lanthanide chelate.

14. The method of claim 13, wherein the fluorophore is a semiconductor nanocrystal.

15. The method of claim 13, wherein the fluorophore is a fluorescent dye.

16. The method of claim 15, wherein the fluorescent dye is fluorescein.

17. The method of claim 13, wherein the fluorophore is a lanthanide chelate.

18. The method of claim 1, wherein the target polynucleotide is DNA.

19. The method of claim 1, wherein the target polynucleotide is RNA.

20. The method of claim 1, wherein the sample comprises single-stranded target polynucleotide.

21. The method of claim 1, wherein the sample comprises double-stranded target polynucleotide.

22. The method of claim 1, wherein the target polynucleotide is produced via an amplification reaction.

23. The method of claim 1, wherein light emitted from the signaling chromophore above a threshold level indicates that the target polynucleotide is present in the sample.

24. The method of claim 1, wherein the amount of light emitted from the signaling chromophore is quantitated and used to determine the amount of the target polynucleotide in the sample.

25. The method of claim 12, wherein the fluorophore is a green fluorescent protein.

26. The method of claim 1, wherein the target polynucleotide is not amplified.

27. The method of claim 1, wherein the method is performed on a substrate.

28. The method of claim 27, wherein the substrate is selected from the group consisting of a microsphere, a chip, a slide, a multiwell plate, an optical fiber, an optionally porous gel matrix, a photodiode, and an optoelectronic device.

29. The method of claim 28, wherein the substrate is a slide.

30. The method of claim 28, wherein the substrate is an optoelectronic device.

31. The method of claim 28, wherein the substrate is an optionally porous gel matrix.

32. The method of claim 31, wherein the substrate is a sol-gel.

33. The method of claim 28, wherein the substrate is nanoaddressable.

34. The method of claim 28, wherein the substrate is microaddressable.

35. The method of claim 28, wherein the substrate is conjugated to a plurality of different sensor polynucleotides having corresponding different sequences, wherein each of said different sensor polynucleotides can selectively hybridize to a corresponding different target polynucleotide.

36. The method of claim 1, wherein the method comprises performing fluorescence in situ hybridization (FISH).

37. The method of claim 22, wherein the amplification reaction comprises a polymerase chain reaction.

38. The method of claim 1, further comprising contacting the sample in a solution comprising the sensor polynucleotide, the multichromophore and a second signaling chromophore that can absorb energy from the signaling chromophore in the presence of target and emit light, and wherein detecting whether the light emitted from the signaling chromophore comprises detecting if light is emitted from the second signaling chromophore.

39. The method of claim 38, wherein the second signaling chromophore is a polynucleotide-specific dye.

40. A signaling complex formed by the method of claim 1.

41. The complex of claim 40, further comprising a second signaling chromophore.

42. A substrate-bound complex formed by the method of claim 27.

43. The substrate-bound complex of claim 42, further comprising a second signaling chromophore.

44. The method of claim 3, wherein the saturated polymer is attached to luminescent dyes.