IP Library › Granted Patent US 11,359,226
Granted Patent B2
US 11,359,226 · App. 16/384,741 · Granted Jun 14, 2022

Contiguity particle formation and methods of use

Inventors: Frank J. Steemers (Encinitas, CA); Ramesh Ramji (San Diego, CA); Steven Norberg (La Mesa, CA); Lena Christiansen (San Diego, CA); Dmitry K. Pokholok (San Diego, CA); Fan Zhang (San Diego, CA)
Assignee: ILLUMINA, INC.
C12Q1/6806A61K47/58A61K47/6937C12M25/16C12N5/0012C12N5/16C12N2533/40
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Quick Facts
Patent No.
US 11,359,226
App. No.
16/384,741
Granted
Jun 14, 2022
Kind
B2
Abstract

Embodiments of systems, methods, and compositions provided herein relate to hollow beads encapsulating single cells. Some embodiments include performing multiple co-assays on a single cell encapsulated within a hollow bead, including nucleic acid sequencing, preparing nucleic acid libraries, determining methylation status, identifying genomic variants, or protein analysis.

Claims (16)

1. A method of performing multiple sequential co-assays on a single cell encapsulated within a hollow bead, comprising:

obtaining a hollow bead encapsulating a single cell, wherein the hollow bead comprises:

a polymer shell comprising PEG-epoxide and amine dissolved in oil or PEG-epoxide and PEG-amine; and

a single cell disposed within the polymer shell,

wherein the polymer shell comprises pores that allow diffusion of reagents through the polymer shell while retaining the single cell; and

sequentially contacting the single cell with the reagents to perform multiple sequential co-assays.

2. The method of claim 1 , wherein an interior of the polymer shell comprises an aqueous environment.

3. The method of claim 1 , wherein the single cell disposed within the polymer shell is free from interaction with the polymer shell and/or is not in contact with the polymer shell.

4. The method of claim 1 , wherein the hollow bead has a diameter of about 20 μm to about 200 μm.

5. The method of claim 1 , wherein the polymer shell comprises a four-arm polyethylene glycol (PEG).

6. The method of claim 1 , wherein the single cell is a mammalian cell.

7. The method of claim 1 , wherein the reagents comprise enzymes, chemicals, and primers having a size of less than 50 base pairs.

8. The method of claim 7 , wherein the reagents comprise one or more of a lysozyme, proteinase K, random hexamers, polymerase, transposase, primers, ligase, catalyzing enzyme, deoxynucleotide triphosphates, buffers, or divalent cations.

9. The method of claim 1 , wherein the multiple sequential co-assays comprise lysis, DNA analysis, RNA analysis, protein analysis, tagmentation, nucleic acid amplification, nucleic acid sequencing, DNA library preparation, assay for transposase accessible chromatin using sequencing (ATAC-seq), contiguity-preserving transposition sequencing (CPT-seq), single cell combinatorial indexed sequencing (SCI-seq), or single cell genome amplification, or any combination thereof performed sequentially.

10. The method of claim 1 , wherein the hollow bead encapsulating a single cell is seeded on a solid support.

11. The method of claim 10 , wherein the solid support is an etched surface, a well, a flow-cell device, a microfluidic channel, a bead, or a column.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 11, 2020
From: STEEMERS, FRANK J; RAMJI, RAMESH; CHRISTIANSEN, LENA; NORBERG, STEVEN; POKHOLOK, DMITRY K; ZHANG, FAN
To: ILLUMINA, INC.
Reel/Frame 052909/0760 →
Continuity (2)
Provisional Application 62660452 · Apr 20, 2018
Related Publication 20190352591A1 · Nov 21, 2019
Cited By (1)
US 12,480,090