IP Library Granted Patent US 10,597,713
Granted Patent B2
US 10,597,713 · App. 15/944,365 · Granted Mar 24, 2020

Hairpin loop method for double strand polynucleotide sequencing using transmembrane pores

Inventors: Clive Gavin Brown (Cambridge, GB); James Anthony Clarke (Oxford, GB); Graham Hall (Oxford, GB); Gavin Harper (Oxford, GB); Andrew John Heron (Oxford, GB); James White (Oxford, GB)
Assignee: Oxford Nanopore Technologies Ltd.
C12Q1/6869G01N27/44717G01N27/44791G01N33/48721
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Quick Facts
Patent No.
US 10,597,713
App. No.
15/944,365
Granted
Mar 24, 2020
Kind
B2
Abstract

The invention relates to a new method of sequencing a double stranded target polynucleotide. The two strands of the double stranded target polynucleotide are linked by a bridging moiety. The two strands of the target polynucleotide are separated using a polynucleotide binding protein and the target polynucleotide is sequenced using a transmembrane pore.

Claims (6)

1. A method for nanopore sensing, the method comprising:

i) coupling a nucleic acid construct transiently to a membrane via a 3′ cholesterol TEG tether,

wherein the membrane comprises an amphiphilic layer that is a 1,2-diphytanoyl-glycero-3-phosphocholine lipid bilayer, and wherein a MspA transmembrane pore is present in the membrane, wherein the MspA transmembrane pore is a nanopore, and is configured to permit flow of ions through the transmembrane pore from one side of the membrane to the other side of the membrane,

wherein the construct comprises a target polynucleotide having a target portion, a leader, and the 3′ cholesterol TEG tether, wherein the construct is configured such that the leader facilitates engagement of the construct with the transmembrane pore while the construct is transiently coupled to the membrane, promoting passage of the nucleic acid construct through the nanopore, and

wherein the step of transiently coupling the construct to the membrane comprises contacting the membrane with the construct, wherein the construct comprises, prior to the contacting step, the target polynucleotide, the leader, and the 3′ cholesterol TEG tether; and

ii) sensing at least the target portion of the target polynucleotide upon movement of the construct through the nanopore, wherein sensing comprises reading nucleotides of the nucleic acid construct as the nucleotides pass through the nanopore in order to sequence the target portion, wherein the nucleotides are read from single channel currents obtained from electrodes connected to a buffered solution on cis and trans sides of the lipid bilayer comprising the nanopore.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 10, 2018
From: BROWN, CLIVE GAVIN; CLARKE, JAMES ANTHONY; HALL, GRAHAM; HARPER, GAVIN; HERON, ANDREW JOHN; WHITE, JAMES
To: OXFORD NANOPORE TECHNOLOGIES LTD.
Reel/Frame 045769/0330 →
Continuity (3)
Continuation 14234698
Provisional Application 61511436 · Jul 25, 2011
Related Publication 20180291441A1 · Oct 11, 2018
Cited By (4)
US 12,448,646 US 12,584,168 US 12,630,851 US 12,716,096