IP Library Granted Patent US 12,359,053
Granted Patent B2
US 12,359,053 · App. 18/233,276 · Granted Jul 15, 2025

Flow cell including a heteropolymer

Inventors: Wayne N. George (Ilford, GB); Ludovic Vincent (San Diego, CA); Andrew A. Brown (Cambridge, GB); Mathieu Lessard-Viger (San Diego, CA)
Assignees: Illumina Inc.; Illumina Cambridge Limited
C08L33/08C08L33/26C12Q1/6853C12Q1/6869
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Quick Facts
Patent No.
US 12,359,053
App. No.
18/233,276
Granted
Jul 15, 2025
Kind
B2
Abstract

A flow cell includes a support and a heteropolymer attached to the support. The heteropolymer includes an acrylamide monomer including an attachment group to react with a functional group attached to a primer, and a monomer including a stimuli-responsive functional group. The monomer including the stimuli-responsive functional group may be pH-responsive, temperature-responsive, saccharide-responsive, nucleophile-responsive, and/or salt-responsive.

Claims (42)

1. A heteropolymer, comprising:

an acrylamide monomer comprising a tetrazine attachment group to react with a functional group attached to a primer; and

a monomer comprising a stimuli-responsive functional group, wherein the monomer comprising the stimuli-responsive functional group is selected from the group consisting of:

an acrylamide monomer including a terminal pH-responsive functional group selected from the group consisting of a hydroxyl with an acid-labile protecting group, a hydroxyl with a base-labile protecting group, 1,2-diol protected as an acetal, hemiacetal, or ketal, 1,3-diol protected as an acetal, hemiacetal, or ketal, a tert-butyloxycarbonylamino group (boc), a 9H-fluoren-9-ylmethoxycarbonylamino group (Fmoc), a carboxylate group, a carboxylic acid group, a sulfonate group, and a sulfonic acid group;

a vinyl or acrylate monomer including a terminal pH-responsive functional group selected from the group consisting of a hydroxyl with an acid-labile protecting group, a hydroxyl with a base-labile protecting group, an amino with an acid-labile protecting group, an amino with a base-labile protecting group, a sulfonate group and a sulfonic acid group;

a temperature-responsive N-substituted acrylamide;

an acrylamide, acrylate, or vinyl monomer including a terminal saccharide-responsive functional group;

an acrylamide, acrylate, or vinyl monomer including a terminal nucleophile-responsive functional group; and

an acrylamide, acrylate, or vinyl monomer including a terminal salt-responsive functional group.

2. The heteropolymer of claim 1 , wherein the monomer comprising the stimuli-responsive functional group is to undergo modification when exposed to a predetermined stimulus, wherein the modification changes the polarity and/or conformation of the heteropolymer.

3. The heteropolymer of claim 1 , further comprising the primer grafted to the attachment group.

4. The heteropolymer of claim 1 , wherein:

the monomer comprising the stimuli-responsive functional group is the acrylamide, acrylate, or vinyl monomer including the terminal saccharide-responsive functional group; and

the terminal saccharide-responsive functional group comprises a boronic acid group.

5. The heteropolymer of claim 4 , wherein the monomer comprising the stimuli-responsive functional group is 3-(acrylamido)phenylboronic acid.

6. The heteropolymer of claim 1 , wherein:

the monomer comprising the stimuli-responsive functional group is the acrylamide, acrylate, or vinyl monomer including the terminal nucleophile-responsive functional group; and

the terminal nucleophile-responsive functional group has the following structure:

wherein: (a) Y is SO2 and Y′ is CH2; or (b) Y and Y′ are both C(O).

7. The heteropolymer of claim 1 , wherein:

the monomer comprising the stimuli-responsive functional group is the acrylamide, acrylate, or vinyl monomer including the terminal salt-responsive functional group; and

the salt-responsive functional group is a zwitterionic functional group exhibiting antipolyelectrolyte behavior.

8. The heteropolymer of claim 7 , wherein the monomer comprising the stimuli-responsive functional group has one of the following structures:

wherein A is O or NH and Rz is H or C1-4alkyl; or

wherein Rz is H or C1-4alkyl.

9. The heteropolymer of claim 1 , wherein:

the monomer comprising the stimuli-responsive functional group is the temperature-responsive N-substituted acrylamide; and

the temperature-responsive N-substituted acrylamide includes a heat-sensitive hydroxyl or amino protecting group.

10. The heteropolymer of claim 1 , wherein:

the monomer comprising the stimuli-responsive functional group is the temperature-responsive N-substituted acrylamide; and

the temperature-responsive N-substituted acrylamide is N-isopropylacrylamide.

11. A flow cell, comprising:

a support; and

the heteropolymer of claim 1 attached to the support.

12. A method of making a flow cell, comprising contacting the heteropolymer of claim 1 with at least a portion of a flow cell support, thereby attaching the heteropolymer to the flow cell support.

13. The method of claim 12 , further comprising grafting a primer to the attachment group of the heteropolymer attached to the support.

14. The method of claim 12 , further comprising exposing the heteropolymer attached to the flow cell support to a predetermined stimulus.

15. The method of claim 14 , further comprising, after the exposing, performing a sequencing operation on the flow cell.

16. The heteropolymer of claim 1 , wherein the acrylamide monomer including the terminal pH-responsive functional group has a structure:

where:

X is —O-Boc, —NHBoc, or —NHFmoc; and

each R z is independently H or C 1-4 alkyl.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2024
From: VINCENT, LUDOVIC; LESSARD-VIGER, MATHIEU
To: ILLUMINA, INC.
Reel/Frame 066071/0367 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2024
From: GEORGE, WAYNE N.; BROWN, ANDREW A.
To: ILLUMINA CAMBRIDGE LIMITED
Reel/Frame 066071/0398 →
Continuity (3)
Continuation 16721451 · Dec 19, 2019
Provisional Application 62792250 · Jan 14, 2019
Related Publication 20230391997A1 · Dec 7, 2023
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