Deterministic control of polymer molecule translocation through a nanopore

Patent metadata

Field	Value
Publication number	US-12416625-B2
Application number	US-202519067493-A
Country	US
Kind code	B2
Filing date	Feb 28, 2025
Priority date	Jun 29, 2017
Publication date	Sep 16, 2025
Grant date	Sep 16, 2025

Abstract

In a method for controlling translocation of a target polymer molecule through a nanopore, a clamp is reversibly bound at a site along the target polymer molecule length; the clamp and the target polymer molecule are disposed in an ionic solution that is in fluidic communication with a nanopore having an aperture diameter less than an outer diameter of the clamp. A constant translocation force is applied across the nanopore to induce travel of the target polymer molecule into the nanopore such that the reversibly bound clamp abuts the nanopore. A voltage pulse is applied across the nanopore that advances the target polymer molecule into the nanopore by one nucleotide, without either of chemical fuel and biochemical fuel provided to the clamp. The voltage pulse is repeatedly applied to cause a plurality of nucleotides to translocate through the nanopore. An indication of each nucleotide can be acquired during nucleotide translocation.

First claim

We claim:

1. A method for controlling translocation of a target polymer molecule through a nanopore, the target polymer molecule having a target polymer molecule length comprising a plurality of nucleotides, comprising:
reversibly binding a clamp to the target polymer molecule at a site along the target polymer molecule length;
disposing the target polymer molecule and the clamp in an ionic solution that is in fluidic communication with the nanopore, the nanopore having an aperture diameter less than an outer diameter of the clamp;
applying a constant translocation force across the nanopore to induce travel of the target polymer molecule in the ionic solution into the nanopore such that the reversibly bound clamp abuts the nanopore;
applying across the nanopore a voltage pulse that advances the target polymer molecule into the nanopore by one nucleotide, without providing either of chemical fuel and biochemical fuel to the clamp; and
repeatedly applying the voltage pulse to cause a plurality of nucleotides to translocate through the nanopore.

2. The method of claim 1 wherein applying a constant translocation force across the nanopore comprises applying a voltage bias across the nanopore.

3. The method of claim 2 wherein applying a voltage pulse comprises applying a voltage pulse having a voltage pulse magnitude greater than a voltage bias magnitude of the voltage bias applied across the nanopore.

4. The method of claim 1 further comprising measuring current through the nanopore while a plurality of nucleotides of the target polymer molecule translocates through the nanopore.

5. The method of claim 1 further comprising acquiring a representative indication of a nucleotide as the nucleotide translocates through the nanopore.

6. The method of claim 5 wherein repeatedly applying the voltage pulse comprises conducting one repetition of voltage pulse application after acquisition of a representative indication of a nucleotide.

7. The method of claim 1 further comprising acquiring a representative indication of a sequence of nucleotides as the plurality of nucleotides translocates through the nanopore.

8. The method of claim 1 wherein reversibly binding a clamp to the target polymer molecule comprises reversibly binding a clamp selected from biological molecule clamp, biochemical clamp, protein clamp, and enzyme clamp to a plurality of nucleotides.

9. The method of claim 1 wherein reversibly binding a clamp to the target polymer molecule comprises reversibly binding a helicase enzyme to a plurality of nucleotides.

10. The method of claim 9 wherein reversibly binding a helicase enzyme to a plurality of nucleotides comprises reversibly binding a helicase enzyme selected from a SF1 family helicase and a T4 Dda helicase to a plurality of nucleotides.

11. The method of claim 1 wherein reversibly binding a clamp to the target polymer molecule comprises reversibly binding a polymerase enzyme to a plurality of nucleotides.

12. The method of claim 1 wherein applying a constant translocation force comprises applying a translocation force selected from electrophoretic force, hydrostatic force, optical force, and magnetic force.

13. The method of claim 1 wherein applying the pulse of force comprises applying a pulse of electrical voltage having an electrical voltage pulse duration less than a length of time required for the constant translocation force to induce the target polymer molecule to travel into the nanopore by one nucleotide.

14. The method of claim 1 wherein applying a voltage pulse comprises applying a voltage pulse having an electrical voltage pulse duration no greater than about one millisecond.

15. The method of claim 1 wherein reversibly binding a clamp to the target polymer molecule comprises first disposing the target polymer molecule in the ionic solution and then reversibly binding the clamp to the target polymer molecule.

16. The method of claim 1 wherein applying a voltage pulse that advances the target polymer molecule into the nanopore by one nucleotide comprises applying a voltage pulse across a biological nanopore selected from a CsgG bacterial porin nanopore and a Mycobacterium smegmatis porin A (MspA) nanopore to advance the target polymer molecule into the biological nanopore by one nucleotide.

17. The method of claim 16 wherein applying a voltage pulse across a biological nanopore comprises applying a voltage pulse across a biological nanopore disposed in a membrane selected from a triblock copolymer membrane, a mycolic acid membrane, a tetraether lipid membrane, and a lipid bilayer membrane.

18. A method for determining a sequence of nucleotides of a target polymer molecule having a target polymer molecule length comprising a plurality of nucleotides, comprising:
reversibly binding a clamp to the target polymer molecule at a site along the target polymer molecule length;
after binding the clamp to the target polymer molecule, disposing the target polymer molecule and the reversibly-bound clamp in an ionic solution that is in fluidic communication with a nanopore, the nanopore having an aperture diameter less than an outer diameter of the clamp;
applying a constant translocation force across the nanopore to induce travel of the target polymer molecule in the ionic solution into the nanopore such that the reversibly bound clamp abuts the nanopore;
applying across the nanopore a voltage pulse that advances the target polymer molecule into the nanopore by one nucleotide, without providing either of chemical fuel and biochemical fuel to the clamp;
acquiring a representative indication of a nucleotide as the nucleotide translocates through the nanopore; and
repeatedly applying the voltage pulse to cause a plurality of nucleotides to translocate through the nanopore, with a repetition of voltage pulse application after each acquisition of a representative indication of a nucleotide.

19. The method of claim 18 wherein applying a constant translocation force across the nanopore comprises applying an electrical voltage bias across the nanopore, and wherein applying a voltage pulse across the nanopore comprises applying a voltage pulse having a voltage pulse amplitude greater than a voltage bias amplitude of the applied electrical voltage bias.

20. A method for determining a sequence of nucleotides of a target polymer molecule having a target polymer molecule length comprising a plurality of nucleotides, comprising:
disposing the target polymer molecule and a clamp in an ionic solution that is in fluidic communication with a nanopore, the nanopore having an aperture diameter less than an outer diameter of the clamp;
after disposing the target polymer molecule and the clamp in an ionic solution, reversibly binding the clamp to the target polymer molecule in the ionic solution at a site along the target polymer molecule length;
applying a constant translocation force across the nanopore to induce travel of the target polymer molecule in the ionic solution into the nanopore such that the reversibly bound clamp abuts the nanopore;
applying across the nanopore a voltage pulse that advances the target polymer molecule into the nanopore by one nucleotide, without providing either of chemical fuel and biochemical fuel to the clamp;
acquiring a representative indication of a nucleotide as the nucleotide translocates through the nanopore; and
repeatedly applying the voltage pulse to cause a plurality of nucleotides to translocate through the nanopore, with one repetition of voltage pulse application a

Assignees

• Harvard College

Inventors

• Branton Daniel
• Fleming Stephen Jordan
• Golovchenko Jene A

Classifications

• G01N27/40

  Semi-permeable membranes or partitions · CPC title

• C12Y306/01039

  Thymidine-triphosphatase (3.6.1.39), i.e. T4 helicase · CPC title

• C12Q1/6869 Primary

  Methods for sequencing · CPC title

• B82Y35/00

  Methods or apparatus for measurement or analysis of nanostructures · CPC title

• B01D71/74

  Natural macromolecular material or derivatives thereof (B01D71/08, B01D71/24 take precedence) · CPC title