Simultaneous amplification and detection of ribonucleic acid be an optical method using surface plasmon resonance

• US 7,998,672 B2
• Filed: 05/30/2007
• Issued: 08/16/2011
• Est. Priority Date: 05/30/2006
• Status: Active Grant

• Current Assignee: University of Utah Research Foundation (State of Utah)
• Original Assignee: University of Utah Research Foundation (State of Utah)
• Inventors: Roper, D. Keith
• Primary Examiner(s): Calamita; Heather
• Application Number:
  US11/809,009
• Publication Number:
  US 20080131939A1
• Time in Patent Office: 1,539 Days
• Field of Search: None
• US Class Current: 435/6.12
• CPC Class Codes: C12Q 1/686 Polymerase chain reaction [PCR]
• CPC Class Codes: C12Q 2561/113 Real time assay
• CPC Class Codes: C12Q 2565/628 being a surface plasmon resonance spectrometer
• CPC Class Codes: G01N 21/554 detecting the surface plasmon resonance of nanostructured metals, e.g. localised surface plasmon resonance
• CPC Class Codes: G01N 21/6428 Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" in vivo A61B5/00; immunoassay G01N33/53
• CPC Class Codes: G01N 21/648 using evanescent coupling or surface plasmon coupling for the excitation of fluorescence
• CPC Class Codes: G01N 33/54373 involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
• CPC Class Codes: G01N 33/587 Nanoparticles

Abstract

Methods of performing PCR are provided. Methods may include using an optical source to provide heating for thermocyling the PCR reaction. Methods may include using surface plasmon resonance and/or fluorescence resonance enhanced transfer to allow real-time monitoring of a PCR reaction. Methods may include immobilizing a template, primer, or polymerase on a surface such as a gold or other surface plasmon resonance active surface.

Claims

1. A method of performing a Polymerase-Chain-Reaction (PCR) using surface plasmon resonance (SPR), the method comprising:

providing a PCR reaction cell that includes a surface plasmon active surface;

contacting the surface plasmon active surface with an aqueous medium comprising or in fluid contact with a template, a primer capable of annealing to the template, dNTPs, and a thermostable polymerase, wherein the aqueous medium, the template, the primer, the dNTPs, and the thermostable polymerase are substantially free of dyes or labels;

performing an SPR-induced PCR amplification with the template, the primer, the dNTPs, and the thermostable polymerase, wherein the SPR-induced PCR amplification includes;

allowing the primer to anneal to the template;

heating a portion of the aqueous medium that is in contact with the surface plasmon active surface by exciting surface plasmons at an interface between the surface plasmon active surface and the aqueous medium so as to induce selective decay of the excited surface plasmons such that decaying surface plasmons heat the aqueous medium adjacent to the surface plasmon active surface to a temperature selected to allow elongation of the primer;

elongating the primer using the thermostable polymerase at the temperature selected to allow elongation of the primer; and

heating a portion of the aqueous medium that is in contact with the surface plasmon active surface by exciting surface plasmons at the interface between the surface plasmon active surface and the aqueous medium so as to induce selective decay of the excited surface plasmons such that decaying surface plasmons heat the aqueous medium adjacent to the surface plasmon active surface to a temperature selected to denature the elongated primer and the template.

2. The method of claim 1, wherein the surface plasmon active surface comprises a surface of a nanoparticle.

3. The method of claim 2, wherein the nanoparticle is selected from the group consisting of surface plasmon active nanoparticles, nanoshells, and nanocylinders.

4. The method according to claim 1, further comprising immobilizing at least one of the template, the primer capable of annealing to the template, and the thermostable polymerase on the surface plasmon active surface.

5. The method according to claim 4, wherein immobilizing at least one of the template, the primer capable of annealing to the template, and the thermostable polymerase on the surface plasmon active surface comprises using N-hydroxysuccinimide.

6. The method according to claim 1, wherein the Polymerase-Chain-Reaction is a multiplex Polymerase-Chain-Reaction.

7. The method according to claim 1, wherein heating the portion of the aqueous medium that is in contact with the surface plasmon active surface to a temperature selected to allow elongation of the primer is performed on a millisecond time scale.

8. The method according to claim 1, wherein heating the portion of the aqueous medium that is in contact with the surface plasmon active surface to a temperature selected to allow denaturation of the elongated primer and the template is performed on a millisecond time scale.

9. The method according to claim 1, further comprising detecting mass elongating of the primer and amplification of the template using surface plasmon resonance.

10. The method according to claim 1, wherein the optical source is capable of emitting light with a wavelength of about 500 nm to about 900 nm.

11. The method according to claim 1, wherein the optical source is selected from the group consisting of a laser, Ti:

sapphire laser, an argon-ion laser, a krypton laser, a xenon lamp, and an light-emitting diode.

19. The method of claim 1, wherein heating portion of the aqueous medium that is in contact with the surface plasmon active surface to allow elongation and denaturation is accomplished without inducing direct bulk heating of the aqueous medium.

20. The method of claim 1, wherein heating portion of the aqueous medium that is in contact with the surface plasmon active surface comprises directly heating an area within about 44 to about 189 nm adjacent to the surface plasmon active surface.

21. The method of claim 1, wherein heating portion of the aqueous medium that is in contact with the surface plasmon active surface comprises directly heating an area within about 189 nm adjacent to the surface plasmon active surface.

12. A method of real time detection of Polymerase-Chain-Reaction (PCR) amplicons by Surface-Plasmon-Resonance (SPR), said method comprising:

immobilizing a polymerase or a polynucleotide primer on a surface plasmon active surface;

providing, in fluid contact with the surface plasmon active surface, a PCR reaction mix that comprises a PCR template, dNTPs, and a polymerase or a polynucleotide primer if not already immobilized on the surface plasmon active surface, wherein the PCR reaction mix is substantially free of dyes or labels;

cycling an annealing temperature, an elongation temperature, and a denaturation temperature of an area within about 189 nm adjacent to the surface plasmon active surface using a first SPR excitation technique so as to perform PCR using the polymerase, primer, PCR template, and dNTPs;

wherein cycling the temperature of an area adjacent the surface plasmon active surface so as to perform PCR comprises heating the area adjacent the surface plasmon active surface by exciting surface plasmons at an interface between the surface plasmon active surface and the aqueous medium so as to induce selective decay of the excited surface plasmons such that decaying surface plasmons heat the aqueous medium adjacent to the surface plasmon active surface; and

measuring rates and magnitudes of interaction between the template and molecules immobilized on the surface plasmon active surface using a second SPR excitation technique that is different than the first SPR excitation technique for analyzing mass-induced changes in resonance absorption, wherein the second SPR excitation technique does not induce heating of the area adjacent the surface plasmon active surface.

13. The method according to claim 12, wherein cycling between the annealing temperature and the elongation temperature occurs on a millisecond time scale.

14. The method according to claim 12, wherein cycling between the elongation temperature and the denaturation temperature occurs on a millisecond time scale.

15. The method according to claim 12 wherein the optical source stimulates surface plasmon resonance.

16. The method according to claim 15, wherein the optical source is capable of emitting light with a wavelength of about 500 nm to about 900 nm.

17. The method according to claim 15, wherein the optical source is selected from the group consisting of a laser, Ti:

sapphire laser, an argon-ion laser, a krypton laser, a xenon lamp, and an light-emitting diode.

18. The method according to claim 12, wherein the surface plasmon active surface comprises a nanoparticle.

22. The method claim 12, wherein the surface plasmon active surface is a gold surface.