IP Library Granted Patent US 10,385,389
Granted Patent B2
US 10,385,389 · App. 15/113,207 · Granted Aug 20, 2019

Method for attaching one or more polynucleotide binding proteins to a target polynucleotide

Inventors: Andrew John Heron (Oxford, GB); Clive Gavin Brown (Cambridge, GB); Rebecca Victoria Bowen (Oxford, GB); James White (Oxford, GB); Daniel John Turner (Oxford, GB); Joseph Hargreaves Lloyd (Oxford, GB); Christopher Peter Youd (Oxford, GB)
Assignee: Oxford Nanopore Technologies Ltd.
C12Q1/6869C12N9/93C12Q1/6816C12Q1/6834C12Y605/01001C12Q2565/631
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Quick Facts
Patent No.
US 10,385,389
App. No.
15/113,207
Granted
Aug 20, 2019
Kind
B2
Abstract

The invention relates to new methods of attaching one or more polynucleotide binding proteins to a target polynucleotide. The invention also relates to new methods of characterizing target polynucleotides.

Claims (25)

1. A method for attaching one or more polynucleotide binding proteins to a target polynucleotide, comprising:

(a) providing the one or more polynucleotide binding proteins bound to one or more loading moieties; and

(b) covalently attaching the one or more loading moieties to the target polynucleotide.

2. A method according to claim 1 , wherein the method comprises before step (a) binding the polynucleotide binding proteins to the one or more loading moieties.

3. A method according to claim 1 , wherein the one or more polynucleotide binding proteins are polynucleotide handling enzymes.

4. A method according to claim 3 , wherein the one or more polynucleotide handling enzymes are one or more polymerases, exonucleases, helicases, topoisomerases or a combination thereof.

5. A method according to claim 4 , wherein the one or more helicases are Hel308 helicases, RecD helicases, XPD helicases or Dda helicases.

6. A method according to claim 5 , wherein the one or more helicases are modified to reduce the size of an opening in the polynucleotide binding domain through which in at least one conformational state the polynucleotide can unbind from the helicase.

7. A method according to claim 1 , wherein the one or more polynucleotide binding proteins remain bound to the one or more loading moieties at the end of the step (b).

8. A method according to claim 1 , wherein (i) the one or more loading moieties are synthetic; and/or (ii) the one or more loading moieties comprise a loading polynucleotide; and/or (iii) the one or more loading moieties comprise a single stranded polynucleotide to which the one or more polynucleotide binding proteins are bound.

9. A method according to claim 1 , wherein the target polynucleotide is a double stranded polynucleotide.

10. A method according to claim 9 , wherein the at least one of the one or more loading moieties is a Y adaptor.

11. A method according to claim 9 , wherein at least one of the one or more loading moieties is a bridging moiety.

12. A method according to claim 11 , wherein the bridging moiety is a hairpin loop.

13. A method according to claim 1 , wherein the one or more loading moieties comprise one or more anchors that are capable of coupling to a membrane.

14. A method according to claim 1 , wherein the one or more loading moieties is a loading polynucleotide and step (b) comprises attaching the one or more loading moieties to the target polynucleotide using a ligase.

15. A method according to claim 14 , wherein the method further comprises (c) removing the ligase from method conditions.

16. A method according to claim 14 , wherein step (b) is performed in the absence of ATP or using gamma-S-ATP (ATPγS) instead of ATP.

17. A method of characterising a target polynucleotide, comprising:

(a) carrying out a method according to claim 1 ;

(b) contacting the target polynucleotide having the one or more attached polynucleotide binding proteins as provided in step (a) with a transmembrane pore such that the one or more polynucleotide binding proteins control the movement of the polynucleotide with respect to the pore; and

(c) taking one or more measurements as the polynucleotide moves with respect to the pore wherein the measurements are indicative of one or more characteristics of the polynucleotide and thereby characterising the target polynucleotide.

18. A method according to claim 17 , wherein the one or more characteristics are selected from (i) the length of the target polynucleotide, (ii) the identity of the target polynucleotide, (iii) the sequence of the target polynucleotide, (iv) the secondary structure of the target polynucleotide and (v) whether or not the target polynucleotide is modified.

19. A method according to claim 17 , wherein the one or more characteristics of the target polynucleotide are measured by (i) electrical measurement and/or optical measurement or (ii) the electrical measurement which is a current measurement, an impedance measurement, a tunneling measurement or a field effect transistor (FET) measurement.

20. A kit for covalently attaching one or more polynucleotide binding proteins to a target polynucleotide, comprising (a) the one or more polynucleotide binding proteins bound to one or more loading moieties and (b) a ligase.

Assignments (2)
CHANGE OF NAME Recorded Mar 28, 2022
From: OXFORD NANOPORE TECHNOLOGIES LIMITED
To: OXFORD NANOPORE TECHNOLOGIES PLC
Reel/Frame 059525/0422 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 7, 2016
From: HERON, ANDREW JOHN; BROWN, CLIVE GAVIN; BOWEN, REBECCA VICTORIA; WHITE, JAMES; TURNER, DANIEL JOHN; LLOYD, JOSEPH HARGREAVES; YOUD, CHRISTOPHER PETER
To: OXFORD NANOPORE TECHNOLOGIES LTD.
Reel/Frame 039967/0004 →
Priority Claims (3)
GB 1406151.9 · Apr 4, 2014 · national
GB 1406155.0 · Apr 4, 2014 · national
GB 1416197.0 · Sep 12, 2014 · national
Continuity (2)
Continuation In Part PCTGB2014050175 · Jan 22, 2014
Related Publication 20170107569A1 · Apr 20, 2017
Cited By (8)
US 12,227,800 US 12,258,375 US 12,275,761 US 12,371,458 US 12,644,879 US 12,662,703 US 12,679,872 US 12,686,886