Electrocatalytic nucleic acid hybridization detection

• US 7,741,033 B2
• Filed: 08/06/2004
• Issued: 06/22/2010
• Est. Priority Date: 05/13/2003
• Status: Active Grant

• Current Assignee: Trustees of Boston College (Boston College)
• Original Assignee: Trustees of Boston College (Boston College)
• Inventors: Taft, Bradford, Kelley, Shana, Gasparac, Rahela, Lapierre-Devlin, Melissa
• Primary Examiner(s): Kapushoc; Stephen
• Assistant Examiner(s): BHAT, NARAYAN KAMESHWAR
• Application Number:
  US10/913,925
• Publication Number:
  US 20050084881A1
• Time in Patent Office: 2,146 Days
• Field of Search: 435/6, 536/23.1, 536/24.3
• US Class Current: 435/6.11
• CPC Class Codes: C12Q 1/6825 Nucleic acid detection involving sensors
• CPC Class Codes: C12Q 2563/113 the label being electroactive, e.g. redox labels
• CPC Class Codes: C12Q 2563/155 Particles of a defined size, e.g. nanoparticles
• CPC Class Codes: C12Q 2563/173 staining/intercalating agent, e.g. ethidium bromide
• CPC Class Codes: G01N 27/3278 involving nanosized elements, e.g. nanogaps or nanoparticles nanopores G01N33/48721; magnetic beads G01N27/745

Abstract

The detection of specific nucleic acid sequences using electrochemical readout would permit the rapid and inexpensive detection and identification of bacterial pathogens and the analysis of human genes. A new assay developed for this purpose is described that harnesses an electrocatalytic process to monitor nucleic acid hybridization. Furthermore, the new assay when used on nanoscale electrodes, provides ultrasensitive detection of nucleic acids.

Claims

1. A method of detecting nucleic acid hybridization between a nucleic acid probe and a target nucleic acid in a sample, the method comprising:

(a) providing a nucleic acid probe immobilized on nanoelectrode ensembles;

(b) contacting under hybridization conditions the nanoelectrode ensembles and the immobilized nucleic acid probe with the sample and a redox pair comprising (i) a nucleic acid binding compound comprising a first transition metal complex that interacts electrostatically with the nucleic acid probe, and (ii) a redox-active probe comprising a second transition metal complex;

wherein the sample and redox pair are in solution; and

(c) measuring an electrocatalytic signal generated by hybridization of the nucleic acid probe and the target nucleic acid in the sample, wherein an increase of the signal detected relative to a signal of a control sample comprising no target nucleic acid, indicates hybridization between the nucleic acid probe and the target nucleic acid, and wherein a decrease in the signal detected relative to that of perfect complementarity between the nucleic acid probe and the target nucleic acid indicates a mismatch between the nucleic acid probe and the target nucleic acid.

2. The method of claim 1, wherein the first transition metal complex comprises a metal selected from the group consisting of cobalt, iron, molybdenum, osmium, ruthenium and rhenium.

3. The method of claim 1, wherein the first transition metal complex is a transition metal ammonium complex.

4. The method of claim 1, the nanoelectrode ensembles comprise a gold nanowire.

5. The method of claim 1, wherein the second transition metal complex comprises a metal selected from the group consisting of iron, cobalt, molybdenum, iridium, osmium and rhenium.

6. The method of claim 1, wherein the second transition metal complex is a transition metal cyanate or chloride complex.

7. The method of claim 1, wherein the nucleic acid probe comprises DNA.

8. The method of claim 1, wherein the target nucleic acid comprises DNA.

9. The method of claim 1, wherein the target nucleic acid comprises RNA.

10. A method of detecting nucleic acid hybridization between a first nucleic acid and a second nucleic acid, the method comprising:

(a) providing the first nucleic acid immobilized on nanoelectrode ensembles;

(b) contacting under hybridization conditions the nanoelectrode ensembles and the immobilized first nucleic acid with a solution suspected of containing the second nucleic acid and containing a redox pair comprising (i) a first transition metal complex that interacts electrostatically with the nucleic acids, and (ii) a redox-active probe comprising a second transition metal complex; and

(c) measuring an electrocatalytic signal generated by hybridization of the first nucleic acid and the second nucleic acid, wherein an increase of the signal detected relative to a signal of a control sample comprising no second nucleic acid, indicates that the nucleic acid hybridization between the first nucleic acid and the second nucleic acid, and wherein a decrease in the signal detected relative to that of perfect complementarity between the first and second nucleic acids indicates a mismatch between the first nucleic acid and the second nucleic acid.

11. The method of claim 10, wherein the first transition metal complex comprises a metal selected from the group consisting of cobalt, iron, molybdenum, osmium, ruthenium and rhenium.

12. The method of claim 10, wherein the first transition metal complex is a transition metal ammonium complex.

13. The method of claim 10, wherein the nanoelectrode ensembles comprise a gold nanowire.

14. The method of claim 10, wherein the second transition metal complex comprises a metal selected from the group consisting of iron, cobalt, molybdenum, iridium, osmium and rhenium.

15. The method of claim 10, wherein the second transition metal complex is a transition metal cyanate or chloride complex.

16. The method of claim 10, wherein the nucleic acid probe comprises DNA.

17. The method of claim 10, wherein the target nucleic acid comprises DNA.

18. The method of claim 10, wherein the target nucleic acid comprises RNA.

19. A method of detecting nucleic acid hybridization between a nucleic acid probe and a target nucleic acid in a sample, the method comprising:

(a) providing a nucleic acid probe immobilized on nanoelectrode ensembles;

(b) contacting under hybridization conditions the nanoelectrode ensembles and the immobilized nucleic acid probe with the sample and a redox pair comprising a first transition metal complex that interacts electrostatically with the nucleic acid probe, and a redox-active probe comprising an ascorbic acid or tripropylamine, wherein the sample and the redox pair are in solution; and

(c) measuring an electrocatalytic signal generated by hybridization of the nucleic acid probe and the target nucleic acid in the sample, wherein an increase of the signal detected relative to a signal of a control sample comprising no target nucleic acid, indicates that the nucleic acid hybridization between the nucleic acid probe and the target nucleic acid, and wherein a decrease in the signal detected relative to that of perfect complementarity between the nucleic acid probe and the target nucleic acid indicates a mismatch between the nucleic acid probe and the target nucleic acid.

20. The method of claim 19, wherein the first transition metal complex comprises a metal selected from the group consisting of cobalt, iron, molybdenum, osmium, ruthenium and rhenium.

21. The method of claim 19, wherein the first transition metal complex is a transition metal ammonium complex.

22. The method of claim 19, the nanoelectrode ensembles comprise a gold nanowire.

23. The method of claim 19, wherein the nucleic acid probe comprises DNA.

24. The method of claim 19, wherein the target nucleic acid comprises DNA.

25. The method of claim 19, wherein the target nucleic acid comprises RNA.

26. A method of detecting nucleic acid hybridization between a first nucleic acid and a second nucleic acid, the method comprising:

(a) providing the first nucleic acid immobilized on nanoelectrode ensembles;

(b) contacting under hybridization conditions the nanoelectrode ensembles and the immobilized first nucleic acid with a solution suspected of containing the second nucleic acid and containing a redox pair comprising (i) a first transition metal complex that interacts electrostatically with the nucleic acids, and (ii) a redox-active probe comprising an ascorbic acid or tripropylamine; and

(c) measuring an electrocatalytic signal generated by hybridization of the first nucleic acid and the second nucleic acid, wherein an increase of the signal detected relative to a signal of a control sample comprising no second nucleic acid, indicates that the nucleic acid hybridization between the first nucleic acid and the second nucleic acid, and wherein a decrease in the signal detected relative to that of perfect complementarity between the first and second nucleic acids indicates a mismatch between the first nucleic acid and the second nucleic acid.

27. The method of claim 26, wherein the first transition metal complex comprises a metal selected from the group consisting of cobalt, iron, molybdenum, osmium, ruthenium and rhenium.

28. The method of claim 26, wherein the first transition metal complex is a transition metal ammonium complex.

29. The method of claim 26, wherein the nanoelectrode ensembles comprise a gold nanowire.

30. The method of claim 26, wherein the first nucleic acid comprises DNA.

31. The method of claim 26, wherein the second nucleic acid comprises DNA.

32. The method of claim 26, wherein the second nucleic acid comprises RNA.