Method of characterising a target polypeptide using a nanopore

Patent metadata

Field	Value
Publication number	US-2024044865-A1
Application number	US-202318357504-A
Country	US
Kind code	A1
Filing date	Jul 24, 2023
Priority date	Dec 2, 2019
Publication date	Feb 8, 2024
Grant date	—

Abstract

Provided herein are methods of characterising a target polypeptide as it moves with respect to a nanopore. Also provided are related kits, systems and apparatuses for carrying out such methods.

First claim

1 . A method of characterising a target polypeptide, comprising
(i) conjugating the target polypeptide to a polynucleotide to form a polynucleotide-polypeptide conjugate; (ii) contacting the conjugate with a polynucleotide-handling protein; (ii) controlling the movement of the polynucleotide with respect to a transmembrane protein pore using the polynucleotide-handling protein; and (iv) taking one or more measurements characteristic of the polypeptide as the conjugate moves with respect to the transmembrane protein pore,
thereby characterising the polypeptide;
wherein the conjugate comprises a leader that facilitates the threading of the conjugate through the transmembrane protein pore.

2 - 8 . (canceled)

9 . The method according to claim 1 , wherein the polynucleotide-handling protein is a helicase.

10 . The method according to claim 1 , wherein the conjugate comprises a plurality of polypeptide sections and/or a plurality of polynucleotide sections.

11 . The method according to claim 1 , wherein the polypeptide has a length of from 2 to about 50 peptide units.

12 . (canceled)

13 . The method according to claim 1 , wherein the polynucleotide has a length of from about 10 to about 1000 nucleotides.

14 . The method according to claim 1 , wherein one or more adapters a are attached to the polynucleotide in the conjugate.

15 . The method according to claim 1 , wherein:
(i) the polynucleotide-handling protein is located on the cis side of the transmembrane protein pore and the polynucleotide-handling protein controls the movement of the conjugate from the cis side of the transmembrane protein pore to the trans side of the transmembrane protein pore; or (ii) the polynucleotide-handling protein is located on the trans side of the transmembrane protein pore and the polynucleotide-handling protein controls the movement of the conjugate from the trans side of the transmembrane protein pore to the cis side of the transmembrane protein pore.

16 - 17 . (canceled)

18 . The method according to claim 1 , wherein the conjugate comprises one or more structures of the form L-{P-N}-P m , wherein:
(a) L is a leader; (b) P is a polypeptide; (c) N comprises a polynucleotide; and (d) m is 0 or 1;  and wherein the method comprises threading the leader (L) through the transmembrane protein pore thereby contacting the polypeptide (P) with the transmembrane protein pore; and
(i) the polynucleotide-handling protein is located on the cis side of the transmembrane protein pore and the method comprises allowing the polynucleotide-handling protein to control the movement of the polynucleotide moiety (N) from the cis side of the transmembrane protein pore to the trans side of the transmembrane protein pore, thereby controlling the movement of the polypeptide (P) through the transmembrane protein pore; or
(ii) the polynucleotide-handling protein is located on the trans side of the transmembrane protein pore and the method comprises allowing the polynucleotide-handling protein to control the movement of the polynucleotide moiety (N) from the trans side of the transmembrane protein pore to the cis side of the transmembrane protein pore, thereby controlling the movement of the polypeptide (P) through the transmembrane protein pore.

19 . The method according to claim 18 , wherein the conjugate comprises one or more structures of the form L-P 1 -N-{P-N} n -P m , wherein:
(a) n is a positive integer; (b) L is a leader; (c) each P, which may be the same or different, is a polypeptide; (d) each N, which may be the same or different, comprises a polynucleotide; and (e) m is 0 or 1;  and wherein the method comprises threading the leader (L) through the transmembrane protein pore thereby contacting polypeptide (P 1 ) with the transmembrane protein pore, and
(i) the polynucleotide-handling protein is located on the cis side of the transmembrane protein pore and the method comprises allowing the polynucleotide-handling protein to control the movement of each polynucleotide (N) sequentially from the cis side of the transmembrane protein pore to the trans side of the transmembrane protein pore, thereby controlling the movement of each polypeptide (P) sequentially through the transmembrane protein pore; or
(ii) the polynucleotide-handling protein is located on the trans side of the transmembrane protein pore and the method comprises allowing the polynucleotide-handling protein to control the movement of each polynucleotide (N) sequentially from the trans side of the transmembrane protein pore to the cis side of the transmembrane protein pore, thereby controlling the movement of each polypeptide (P) sequentially through the transmembrane protein pore

20 . The method according to claim 1 , wherein:
(i) the polynucleotide-handling protein is located on the cis side of the transmembrane protein pore and the polynucleotide-handling protein controls the movement of the conjugate from the trans side of the transmembrane protein pore to the cis side of the transmembrane protein pore; or (ii) the polynucleotide-handling protein is located on the trans side of the transmembrane protein pore and the polynucleotide-handling protein controls the movement of the conjugate from the cis side of the transmembrane protein pore to the trans side of the transmembrane protein pore.

21 - 22 . (canceled)

23 . The method according to claim 1 , wherein the conjugate comprises one or more structures of the form L-{P-N}-P m , wherein:
(a) L is a leader; (b) P is a polypeptide; (c) N comprises a polynucleotide; (d) m is 0 or 1;  and wherein the method comprises threading the leader (L) through the transmembrane protein pore thereby contacting the polypeptide (P) with the transmembrane protein pore, and
(i) the polynucleotide-handling protein is located on the cis side of the transmembrane protein pore and the method comprises allowing the polynucleotide-handling protein to control the movement of the polynucleotide (N) from the trans side of the transmembrane protein pore to the cis side of the transmembrane protein pore, thereby controlling the movement of the polypeptide (P) through the transmembrane protein pore; or
(i) the polynucleotide-handling protein is located on the trans side of the transmembrane protein pore and the method comprises allowing the polynucleotide-handling protein to control the movement of the polynucleotide (N) from the cis side of the transmembrane protein pore to the trans side of the transmembrane protein pore, thereby controlling the movement of the polypeptide (P) through the transmembrane protein pore.

24 . (canceled)

25 . The method according to claim 1 , wherein the one or more measurements are characteristic of one or more characteristics of the polypeptide selected from (i) the length of the polypeptide, (ii) the identity of the polypeptide, (iii) the sequence of the polypeptide, (iv) the secondary structure of the polypeptide and (v) whether or not the polypeptide is modified.

26 - 31 . (canceled)

32 . The method according to claim 1 , wherein the leader comprises a polynucleotide or a charged polymer.

33 . The method according to claim 1 , wherein the conjugate comprises one or more structures of the form L-{P-N}-P m , wherein:
(a) L is a leader; (b) P is a polypeptide; (c) N comprises a polynucleotide; and (d) m is 0 or 1;
and wherein the method comprises threading the leader (L) through the transmembrane protein pore thereby contacting the polypeptide (P) with the tr

Assignees

• Oxford Nanopore Tech Plc

Inventors

• Heron Andrew John
• Graham James Edward
• Strycharska Melania Slawa

Classifications

• G01N2458/00

  Labels used in chemical analysis of biological material · CPC title

• C12N2310/3517

  Marker; Tag · CPC title

• G01N33/48721 Primary

  Investigating individual macromolecules, e.g. by translocation through nanopores (Coulter counters in general G01N15/12; fabrication methods for nanoscale apertures B81B1/00; sequencing of nucleic acids C12Q1/68) · CPC title

• G01N33/6818 Primary

  Sequencing of polypeptides · CPC title

• C12N15/11

  DNA or RNA fragments; Modified forms thereof (DNA or RNA not used in recombinant technology, C07H21/00); {Non-coding nucleic acids having a biological activity} · CPC title