Method of repeatedly moving a double-stranded polynucleotide through a nanopore

Patent metadata

Field	Value
Publication number	US-2023227902-A1
Application number	US-202118010824-A
Country	US
Kind code	A1
Filing date	Jun 18, 2021
Priority date	Jun 18, 2020
Publication date	Jul 20, 2023
Grant date	—

Abstract

Provided herein is a method of moving a double-stranded polynucleotide with respect to a nanopore using a motor protein. The method allows a portion of the polynucleotide to be interrogated by the pore multiple times. Also provided are polynucleotide adapters and kits comprising such adapters. The methods find use in characterising polynucleotides, for example in sequencing.

First claim

1 . A method of moving a double-stranded polynucleotide with respect to a nanopore, comprising:
a) contacting the polynucleotide with a motor protein and a nanopore; b) allowing the double-stranded polynucleotide to move in a first direction with respect to the nanopore under conditions such that (i) a first portion of the double-stranded polynucleotide dehybridises and (ii) the motor protein controls the movement of one strand of the first portion of the double-stranded polynucleotide in the first direction with respect to the nanopore; c) allowing the double-stranded polynucleotide to move in a second direction with respect to the nanopore under conditions such that (i) the strand of the first portion of the double stranded polynucleotide moves in the second direction with respect to the nanopore and (ii) at least part of the first portion of the polynucleotide rehybridises; and d) allowing the double-stranded polynucleotide to move in the first direction with respect to the nanopore under conditions such that (i) a second portion of the double-stranded polynucleotide dehybridises and (ii) the motor protein controls the movement of one strand of the second portion of the double-stranded polynucleotide in the first direction with respect to the nanopore;
wherein the active double stranded polynucleotide-unwinding activity of the motor protein is suppressed.

2 . A method according to claim 1 , wherein the first portion of the double-stranded polynucleotide is the same as the second portion of the double-stranded polynucleotide.

3 . A method according to claim 1 , wherein the first portion of the double-stranded polynucleotide partially overlaps with the second portion of the double-stranded polynucleotide.

4 . A method according to any one of the preceding claims, further comprising:
e) allowing the double-stranded polynucleotide to move in the second direction with respect to the nanopore under conditions such that (i) the strand of the second portion of the double stranded polynucleotide moves in the second direction with respect to the nanopore and (ii) at least part of the second portion of the polynucleotide rehybridises.

5 . A method according to claim 4 , wherein steps (d) and (e) are repeated multiple times.

6 . A method according to claim 5 , wherein, at each repeat, the second portion of the double-stranded polynucleotide partially overlaps with the second portion of the double-stranded polynucleotide of the preceding repeat.

7 . A method according to any one of the preceding claims, wherein allowing the double-stranded polynucleotide to move in the first direction with respect to the nanopore comprises applying a first force to the double-stranded polynucleotide.

8 . A method according to claim 7 , wherein the first force exceeds the rehybridization force of the polynucleotide.

9 . A method according to any one of the preceding claims, wherein allowing the double-stranded polynucleotide to move in the second direction with respect to the nanopore comprises applying a second force to the double-stranded polynucleotide.

10 . A method according to claim 9 , wherein the second force is applied in the same direction relative to the nanopore as the first force, and the second force is exceeded by the rehybridization force of the polynucleotide.

11 . A method according to any one of claims 7 to 10 , wherein the first force and/or the second force comprises a voltage potential.

12 . A method according to claim 11 , wherein the first force comprises a voltage potential and the second force comprises a voltage potential, and the first force is greater than the second force.

13 . A method according to any one of claims 9 to 12 , wherein the second force is applied in the opposite direction relative to the nanopore as the first force.

14 . A method according to any one of claims 9 to 13 , wherein the second force comprises a force applied by a polynucleotide-handling enzyme which moves the polynucleotide in the second direction relative to the nanopore.

15 . A method according to any one of claims 7 to 14 , wherein the first force comprises a voltage potential and the second force comprises (i) a voltage potential applied in the same direction relative to the nanopore as the first force; and (ii) a force applied by a polynucleotide-handling enzyme which moves the polynucleotide in the opposite direction relative to the nanopore as the first force;
and wherein the component of the second force applied by the polynucleotide-handling enzyme exceeds the component of the second force applied by the voltage potential.

16 . A method according to claim 14 or 15 , wherein the polynucleotide-handling enzyme is a helicase or a variant thereof; preferably wherein the polynucleotide-handling enzyme comprises the sequence of SEQ ID NO: 7 or a variant thereof or the sequence of SEQ ID NO: 8 or a variant thereof.

17 . A method according to any one of the preceding claims, wherein the movement of the polynucleotide in the first direction is faster than the movement of the polynucleotide in the second direction.

18 . A method according to any one of the preceding claims, wherein the active double stranded polynucleotide-unwinding activity of the motor protein is suppressed by omitting fuel for the motor protein from the reaction medium.

19 . A method according to any one of the preceding claims, wherein the motor protein is a variant in which NTP binding and/or hydrolysis is abolished or suppressed.

20 . A method according to any one of the preceding claims, wherein the motor protein is a variant in which DNA-processing activity is abolished or suppressed.

21 . A method according to any one of the preceding claims, wherein the motor protein is a helicase variant in which the pin domain has been removed or reduced.

22 . A method according to claim any one of the preceding claims, wherein the motor protein is a helicase or a variant thereof; preferably wherein the motor protein comprises the sequence of SEQ ID NO: 6 or a variant thereof.

23 . A method of characterising a double-stranded polynucleotide analyte, comprising carrying out a method according to any one of claims 1 to 22 ; wherein one or more of steps (b), (c), (d) and (e) if present comprise taking one or more measurements as the double stranded polynucleotide moves with respect to the nanopore, wherein the one or more measurements are indicative of one or more characteristics of the polynucleotide, and thereby characterising the polynucleotide as it moves with respect to the nanopore

24 . A method of characterising a target double-stranded polynucleotide analyte, comprising:
a) contacting the polynucleotide with a motor protein and a nanopore; b1) allowing the double-stranded polynucleotide to move in a first direction with respect to the nanopore under conditions such that (i) a first portion of the double-stranded polynucleotide dehybridises and (ii) the motor protein controls the movement of one strand of the first portion of the double-stranded polynucleotide in the first direction with respect to the nanopore; b2) taking one or more or more measurements indicative of one or more characteristics of the target polynucleotide as the double stranded polynucleotide moves in the first direction with respect to the nanopore; c1) allowing the double-stranded polynucleotide to move in a second direction with respect to the nanopore under conditions such that (i

Assignees

• Oxford Nanopore Tech Plc

Inventors

• Graham James Edward
• Youd Christopher Peter
• Brown Clive Gavin
• Crawford Marion Louise
• Heron Andrew John
• White James

Classifications

• C12Q1/6869 Primary

  Methods for sequencing · CPC title