Polynucleotide sequencing method

Patent metadata

Field	Value
Publication number	US-9476094-B2
Application number	US-47803602-A
Country	US
Kind code	B2
Filing date	May 20, 2002
Priority date	May 18, 2001
Publication date	Oct 25, 2016
Grant date	Oct 25, 2016

Abstract

The subject invention pertains to a method for determining the sequence of a polynucleotide comprising the steps of (i) contacting a polynucleotide processive enzyme immobilised in a fixed position, with a target polynucleotide under conditions sufficient to induce enzyme activity; (ii) detecting an effect consequent on the interaction of the enzyme and polynucleotide, wherein the effect is detected by measurement of a non-linear optical signal or a linear signal coupled to a non-linear signal.

First claim

The invention claimed is:

1. A method for determining the sequence of a polynucleotide, consisting essentially of the sequential steps of:
(i) contacting a polynucleotide processive enzyme immobilised in a fixed position having a metal nanoparticle positioned on or proximal to the enzyme with a target polynucleotide to form a complex;
(ii) contacting the complex with one or more nucleoside triphosphates selected from the group consisting of dATP, dTTP, dGTP, and dCTP, under conditions sufficient to induce polynucleotide processive enzyme activity;
(iii) generating a non-linear optical signal in the area encompassing at least a portion of the immobilized enzyme; and
(iv) detecting an effect as the complex interacts with the one or more nucleoside triphosphates, by measurement of the non-linear optical signal, wherein the non-linear optical signal measurement consists of measuring the second or third harmonic signals, thereby determining the sequence of the polynucleotide.

2. The method according to claim 1 , wherein the enzyme is a polymerase.

3. The method according to claim 1 , wherein the enzyme is a helicase or primase enzyme.

4. The method according to claim 1 , wherein the nanoparticle is a gold or silver nanoparticle.

5. The method according to claim 1 , wherein there are a plurality of enzymes immobilised on the solid support.

6. The method according to claim 1 , wherein the solid support has a roughened metal surface.

7. The method according to claim 1 , further comprising the application of localised surface plasmon resonance.

8. The method according to claim 5 , wherein the solid support has a roughened metal surface.

9. The method according to claim 5 , wherein the support is silver or gold.

10. The method of claim 1 further comprising immobilizing the polynucleotide processive enzyme on a solid support prior to contacting the enzyme with a target polynucleotide.

11. The method of claim 1 , wherein steps (ii)-(iv) are repeated utilizing the same complex.

12. A method for determining the sequence of a polynucleotide, comprising the sequential steps of:
(i) contacting a polynucleotide processive enzyme immobilised in a fixed position having a metal nanoparticle positioned on or proximal to the enzyme with a target polynucleotide to form a complex;
(ii) contacting the complex with one or more nucleoside triphosphates selected from the group consisting of dATP, dTTP, dGTP, and dCTP, under conditions sufficient to induce polynucleotide processive enzyme activity;
(iii) generating a surface plasmon/evanescent field in an area encompassing at least a portion of the immobilized enzyme;
(iv) generating a non-linear optical signal in the area encompassing at least a portion of the immobilized enzyme, wherein the non-linear imaging signal is generated utilizing a near infrared laser, and wherein the non-linear optical signal is coupled to the surface plasmon/evanescent field signal such that the surface plasmon/evanescent field enhances the signal-to-noise ratio of the non-linear signal; and
(v) detecting an effect as the complex interacts with the one or more nucleoside triphosphates, thereby determining the sequence of the polynucleotide, wherein the effect is detected by measurement of the non-linear signal, and wherein the non-linear optical detection is second or third harmonic generation imaging.

13. The method of claim 12 , wherein the effect detected is a change in conformation of the enzyme.

14. The method of claim 12 , wherein the surface plasmon/evanescent field signal is monitored to analyze the coupling of the non-linear field with the plasmon/evanescent field.

15. The method according to claim 12 , wherein there are a plurality of enzymes immobilised on the solid support.

16. The method of claim 12 further comprising immobilizing the polynucleotide processive enzyme on a solid support prior to contacting the enzyme with a target polynucleotide.

17. The method of claim 12 , wherein steps (ii)-(v) are repeated utilizing the same complex.

Assignees

• Densham Daniel Henry
• Gen Probe Inc

Inventors

• Densham Daniel Henry

Classifications

• C12Q1/6869 Primary

  Methods for sequencing · CPC title

• C12Q2565/632

  being a surface enhanced, e.g. resonance, Raman spectrometer · CPC title

• C12Q2521/543

  Immobilised enzyme(s) · CPC title

• C12Q2533/101

  Primer extension · CPC title

• B82Y5/00

  Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery · CPC title