IP Library Granted Patent US 12,523,644
Granted Patent B2
US 12,523,644 · App. 18/499,069 · Granted Jan 13, 2026

Methods and systems for nucleic acid sequencing using nanopores

Inventors: Justin P. Kinney (San Jose, CA); Daniel Bedau (San Jose, CA)
Assignee: Western Digital Technologies, Inc.
G01N33/48721
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Quick Facts
Patent No.
US 12,523,644
App. No.
18/499,069
Granted
Jan 13, 2026
Kind
B2
Abstract

A method of performing nucleic acid sequencing may comprise using a disintegrator situated in a fluidic channel of a sequencing device to cleave off a portion of a nucleic acid molecule in the fluidic channel; applying an electrostatic force to divert the portion of the nucleic acid molecule through a nanopore; detecting an ionic current through the nanopore; and determining an identity of at least one nucleotide of the portion of the nucleic acid molecule based at least in part on the ionic current. A system for sequencing nucleic acids may comprise an array comprising a plurality of sequencing devices, each comprising a fluidic channel, a disintegrator embedded in the fluidic channel, and a nanopore coupled to an exit end of the fluidic channel; and detection circuitry coupled to the array and configured to detect ionic currents through the nanopores.

Claims (39)

1 . A method of performing nucleic acid sequencing, the method comprising:

using a disintegrator situated in a fluidic channel of a sequencing device, cleaving off a portion of a nucleic acid molecule in the fluidic channel, wherein operation of the disintegrator is enhanced by an assistive element;

applying an electrostatic force to divert the portion of the nucleic acid molecule through a nanopore;

detecting an ionic current through the nanopore; and

determining an identity of at least one nucleotide of the portion of the nucleic acid molecule based at least in part on the ionic current.

2 . The method of claim 1 , wherein cleaving off the portion of the nucleic acid molecule comprises inducing electrolysis.

3 . The method of claim 1 , wherein cleaving off the portion of the nucleic acid molecule comprises exposing a contents of the fluidic channel to UVA radiation.

4 . The method of claim 1 , further comprising controlling a speed of the nucleic acid molecule through the disintegrator.

5 . A method of performing nucleic acid sequencing, the method comprising:

using a disintegrator situated in a fluidic channel of a sequencing device, cleaving off a portion of a nucleic acid molecule in the fluidic channel;

applying an electrostatic force to divert the portion of the nucleic acid molecule through a nanopore;

detecting an ionic current through the nanopore; and

determining an identity of at least one nucleotide of the portion of the nucleic acid molecule based at least in part on the ionic current,

wherein detecting the ionic current through the nanopore comprises sampling the ionic current a plurality of times while the portion of the nucleic acid molecule traverses the nanopore.

6 . The method of claim 5 , wherein the portion of the nucleic acid molecule is a single nucleotide, and the identity of the at least one nucleotide of the portion of the nucleic acid molecule is an identity of the single nucleotide.

7 . The method of claim 5 , wherein cleaving off the portion of the nucleic acid molecule comprises a catalytic moiety cleaving off the portion of the nucleic acid molecule.

8 . The method of claim 7 , wherein the catalytic moiety comprises a divalent cation.

9 . The method of claim 5 , wherein cleaving off the portion of the nucleic acid molecule comprises applying chemical hydrolysis.

10 . The method of claim 5 , further comprising straightening the nucleic acid molecule before cleaving off the portion of the nucleic acid molecule.

11 . The method of claim 10 , wherein straightening the nucleic acid molecule comprises directing the nucleic acid molecule through a structure situated in the fluidic channel.

12 . The method of claim 5 , further comprising controlling a speed of the nucleic acid molecule through the disintegrator.

13 . The method of claim 12 , wherein controlling the speed of the nucleic acid molecule through the disintegrator comprises applying a voltage through an electrode pair to control the speed of the nucleic acid molecule through the disintegrator.

14 . The method of claim 12 , wherein controlling the speed of the nucleic acid molecule through the disintegrator comprises applying hydrostatic pressure to control the speed of the nucleic acid molecule through the disintegrator.

15 . A system for sequencing nucleic acids, the system comprising:

an array comprising a plurality of sequencing devices, each of the plurality of sequencing devices in the array comprising a respective fluidic channel, a respective disintegrator embedded in the respective fluidic channel, and a respective nanopore coupled to an exit end of the respective fluidic channel; and

detection circuitry coupled to the array and configured to detect a plurality of nanopore currents, each of the plurality of nanopore currents corresponding to a respective sequencing device in the array,

wherein each respective fluidic channel comprises a respective horizontal portion and a respective vertical portion.

16 . The system recited in claim 15 , wherein each of the plurality of sequencing devices in the array further comprises a respective straightener.

17 . The system recited in claim 16 , wherein the respective straightener comprises at least one of: (a) a progressive geometry, (b) a quasi-two-dimensional structure, (c) a three-dimensional structure, (d) a plurality of pillars, (e) a funnel, or (f) a plurality of spheres.

18 . The system recited in claim 15 , wherein each respective nanopore is situated at an exit end of the respective vertical portion of the respective fluidic channel.

19 . The system recited in claim 15 , wherein a thickness of each respective nanopore is larger than a pitch of a single nucleotide.

20 . The system recited in claim 15 , wherein each respective disintegrator comprises a catalytic moiety embedded in the respective fluidic channel.

21 . The system recited in claim 20 , wherein the catalytic moiety comprises a divalent cation.

22 . The system recited in claim 15 , wherein each respective disintegrator is configured to apply chemical hydrolysis.

23 . The system recited in claim 15 , wherein the array further comprises a wire, and further comprising a power source coupled to the wire and configured to induce electrolysis.

24 . The system recited in claim 15 , wherein each respective disintegrator comprises a respective waveguide configured to generate evanescent waves to expose a contents of the respective fluidic channel to UVA radiation.

25 . The system recited in claim 15 , wherein:

each respective horizontal portion includes a respective bottom surface defined by a top side of a substrate, and

each respective nanopore is in a membrane situated on a back side of the substrate, the back side of the substrate being distal from the top side of the substrate.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 24, 2025
From: SANDISK TECHNOLOGIES, INC.
To: WESTERN DIGITAL TECHNOLOGIES, INC.
Reel/Frame 070313/0840 →
SECURITY AGREEMENT (SUPPLEMENTAL) Recorded Nov 14, 2024
From: SANDISK TECHNOLOGIES, INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 069411/0486 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 11, 2024
From: WESTERN DIGITAL TECHNOLOGIES, INC.
To: SANDISK TECHNOLOGIES, INC.
Reel/Frame 069169/0572 →
PATENT COLLATERAL AGREEMENT (DDTL) Recorded Feb 22, 2024
From: WESTERN DIGITAL TECHNOLOGIES, INC.
To: JPMORGAN CHASE BANK, N.A., AS THE AGENT
Reel/Frame 066648/0206 →
PATENT COLLATERAL AGREEMENT (AR) Recorded Feb 22, 2024
From: WESTERN DIGITAL TECHNOLOGIES, INC.
To: JPMORGAN CHASE BANK, N.A., AS THE AGENT
Reel/Frame 066648/0284 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 31, 2023
From: KINNEY, JUSTIN P.; BEDAU, DANIEL
To: WESTERN DIGITAL TECHNOLOGIES, INC.
Reel/Frame 065411/0156 →
Continuity (1)
Related Publication 20250137991A1 · May 1, 2025
References Cited (26)
US 9017937B1 · Turner · 2015 [cited by examiner]
US 10883140B2 · Church et al. · 2021 [cited by applicant]
US 20110224098A1 · Luan et al. · 2011 [cited by applicant]
US 20130240359A1 · Turner et al. · 2013 [cited by applicant]
US 20140051068A1 · Cherf et al. · 2014 [cited by applicant]
US 20160153105A1 · Gumbercht · 2016 [cited by applicant]
US 20190309008A1 · Ju et al. · 2019 [cited by applicant]
US 20200038868A1 · So et al. · 2020 [cited by applicant]
US 20200318180A1 · Gunderson et al. · 2020 [cited by applicant]
US 20210268503A1 · Soper · 2021 [cited by examiner]
US 20220299472A1 · Maney, Jr. et al. · 2022 [cited by applicant]
US 20230176032A1 · Bedau et al. · 2023 [cited by applicant]
US 20230176033A1 · Bedau et al. · 2023 [cited by applicant]
International Search Report and Written Opinion from PCT App. No. PCT/US2024/035679 (filed Jun. 26, 2024), mailed Oct. 18, 2024. [cited by applicant]
Breyer, W.A. and Matthews, B.W., Structure of [cited by applicant]
Kumarevel, T., Mizuno, H. and Kumar, P.K., Characterization of the metal ion binding site in the anti-terminator protein, HutP, of Bacillus subtilis. Nucleic acids research, 33(17), pp. 5494-5502, 2005. [cited by applicant]
Lau, M.W., Trachman, R.J. and Ferré-D'Amaré, A.R., A divalent cation dependent variant of the glmS ribozyme with stringent Ca2+ selectivity cooptsa preexisting nonspecific metal ion-binding site. Rna, 23(3), pp. 355-364… [cited by applicant]
Lovett, S.T., The DNA exonucleases of [cited by applicant]
Lu, D. and Keck, J.L., Structural basis of [cited by applicant]
Mcbride, M.B., Reactions controlling heavy metal solubility in soils. Advances in Soil Science: vol. 10, pp. 1-56, 1989. [cited by applicant]
Wang, C. et al., “Clog-free translocation of long DNA in nanofluidic pillar arrays and 30 nm wide channels: A fabrication and hydrodynamic study.” in 18th International Conference on Miniaturized Systems for Chemistry a… [cited by applicant]
Werner, J.H., Cai, H., Keller, R.A. and Goodwin, P.M., Exonuclease I hydrolyzes DNA with a distribution of rates. Biophysical journal, 88(2), pp. 1403-1412, 2005. [cited by applicant]
Yusuke Goto et al., “Silicon nitride nanopore created by dielectric breakdown with a divalent cation: deceleration of translocation speed and identification of single nucleotides,” Nanoscale, Issue 30, 2019. [cited by applicant]
Yusuke Goto et al., Electronic Supplementary Information for “Silicon nitride nanopore created by dielectric breakdown with a divalent cation:deceleration of translocation speed and identification of single nucleotides,… [cited by applicant]
International Search Report and Written Opinion from PCT Application No. PCT/US2024/039072 (filed Jul. 23, 2024), mailed Nov. 4, 2024. [cited by applicant]
Office Action dated Aug. 18, 2025 from U.S. Appl. No. 18/499,024 (filed Oct. 31, 2025). [cited by applicant]