US2009029383A1PendingUtilityA1

Polynucleotide Sequencing Method

Assignee: DENSHAM DANIEL HENRYPriority: May 18, 2001Filed: Sep 8, 2008Published: Jan 29, 2009
Est. expiryMay 18, 2021(expired)· nominal 20-yr term from priority
Inventors:Daniel Densham
C12Q 1/6869B82Y 5/00C12Q 1/68
63
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Claims

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.

Claims

exact text as granted — not AI-modified
1 . 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. 
     
     
         2 . The method according to  claim 1 , wherein the effect is detected by measurement of a non-linear signal. 
     
     
         3 . The method according to  claim 1 , wherein the non-linear optical detection is second or third harmonic generation imaging. 
     
     
         4 . The method according to  claim 1 , wherein the non-linear optical detection is Raman spectroscopy or surface enhanced Raman spectroscopy. 
     
     
         5 . The method according to  claim 1 , wherein a dipolar molecule is positioned on or proximal to the enzyme. 
     
     
         6 . The method according to  claim 5 , wherein the molecule is a styryl dye molecule. 
     
     
         7 . The method according to  claim 5 , wherein the molecule is green fluorescent protein. 
     
     
         8 . The method according to  claim 5 , wherein the dipolar molecule is attached to the individual bases of the polynucleotide. 
     
     
         9 . The method according to  claim 1 , wherein the enzyme is a polymerase. 
     
     
         10 . The method according to  claim 1 , wherein the enzyme is a helicase or primase enzyme. 
     
     
         11 . The method according to  claim 11 , wherein step (i) comprises the addition of the nucleoside triphosphates dATP, dTTP, dGTP and dCTP. 
     
     
         12 . The method according to  claim 11 , wherein the nucleoside triphosphates comprise one or more blocking groups which can be removed selectively by pulsed monochromatic light. 
     
     
         13 . The method according to  claim 1 , wherein a metal nanoparticle is positioned on or proximal to the enzyme. 
     
     
         14 . The method according to  claim 13 , wherein the nanoparticle is a gold or silver nanoparticle. 
     
     
         15 . The method according to  claim 13 , wherein the nanoparticle is incorporated onto one or more of the individual bases of the polynucleotide. 
     
     
         16 . The method according to  claim 1 , wherein the enzyme is immobilised on a solid support. 
     
     
         17 . The method according to  claim 16 , wherein there are a plurality of enzymes immobilised on the solid support. 
     
     
         18 . The method according to  claim 16 , wherein the solid support has a roughened metal surface. 
     
     
         19 . The method according to  claim 16 , wherein the support is silver or gold. 
     
     
         20 . The method according to  claim 1 , wherein detection is carried out in conjunction with Atomic Force Microscopy or Near-Field Scanning Optical Microscopy. 
     
     
         21 . The method according to  claim 1 , further comprising the application of localised surface plasmon resonance. 
     
     
         22 . The method according to  claim 1 , wherein the enzyme is immobilised in a fixed position within a cell. 
     
     
         23 . A solid support material, comprising:
 i) at least one immobilised polymerase and at least one dipolar molecule positioned on or proximal to the polymerase; or   ii) a cell immobilised thereon, wherein the cell comprises a polymerase enzyme maintained in a fixed position within the cell.   
     
     
         24 . An imaging system set up to detect a non-linear optical signal, comprising a solid support having immobilised thereon an enzyme that interacts with a polynucleotide, and a dipolar molecule positioned on or proximal to the enzyme.

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