In situ-generated microfluidic assay structures, related kits, and methods of use thereof

Patent metadata

Field	Value
Publication number	US-11454629-B2
Application number	US-202016908265-A
Country	US
Kind code	B2
Filing date	Jun 22, 2020
Priority date	Dec 8, 2015
Publication date	Sep 27, 2022
Grant date	Sep 27, 2022

Abstract

In situ-generated microfluidic capture structures incorporating a solidified polymer network, methods of preparation and use, compositions and kits therefor are described. Microfluidic capture structures may be advantageously used for assays performed within the microfluidic environment, providing flexibility in assaying micro-objects such as biological cells. Assay reagents and analytes may be incorporated within the microfluidic capture structures.

First claim

What is claimed is:

1. A microfluidic device comprising:
an enclosure comprising a substrate and microfluidic circuit material, the enclosure defining a flow region and a sequestration pen, each located within the enclosure; and
an in situ-generated capture structure disposed within the sequestration pen, wherein the in situ-generated capture structure comprises a solidified polymer network, wherein the solidified polymer network comprises a functionalized site; and further wherein the in situ-generated capture structure permits export of a micro-object from the microfluidic device.

2. The microfluidic device of claim 1 , wherein the solidified polymer network comprises an assay reagent or assay analyte.

3. The microfluidic device of claim 1 , wherein the sequestration pen comprises an isolation region and a connection region, the connection region having a proximal opening to the flow region and a distal opening to the isolation region.

4. The microfluidic device of claim 3 , wherein the in situ-generated capture structure is disposed within the isolation region of the sequestration pen.

5. The microfluidic device of claim 2 , wherein the assay reagent is non-covalently attached to the solidified polymer network.

6. The microfluidic device of claim 2 , wherein the assay reagent comprises a protein, a nucleic acid, an organic molecule, and/or a saccharide.

7. The microfluidic device of claim 6 , wherein the assay reagent comprises an antibody.

8. The microfluidic device of claim 1 , wherein two or more in situ-generated capture structures are disposed in the sequestration pen.

9. The microfluidic device of claim 1 , wherein the solidified polymer network comprises a photoinitiated polymer.

10. The microfluidic device of claim 1 , wherein the solidified polymer network comprises a synthetic polymer, a modified synthetic polymer, a biological polymer, or any combination thereof.

11. The microfluidic device of claim 1 , wherein the substrate is configured to generate dielectrophoresis (DEP) forces within the enclosure.

12. The microfluidic device of claim 1 , wherein the in situ-generated capture structure is affixed to a portion of the microfluidic device.

13. The microfluidic device of claim 1 , wherein the in situ-generated capture structure is affixed to a portion of the at least one sequestration pen.

14. The microfluidic device of claim 1 , wherein the functionalized site comprises a reactive moiety configured to bind an assay analyte or an assay reagent.

15. The microfluidic device of claim 14 , wherein the reactive moiety is configured to react with the assay analyte or the assay reagent via a non-covalent binding, a covalent binding, or an association.

16. The microfluidic device of claim 14 , wherein the reactive moiety comprises an antibody, an antigen, a biotin, a streptavidin, an avidin, an alkynyl moiety, an azido moiety, a chelating moiety, an oligonucleotide hybridization sequence, a cell recognition motif, or a combination thereof.

17. The microfluidic device of claim 16 , wherein the cell recognition motif is an arginylglycylaspartic acid (RGD) peptide motif.

18. The microfluidic device of claim 16 , wherein the reactive moiety comprises N-hydroxysuccinimidyl (NHS).

19. The microfluidic device of claim 14 , wherein the assay analyte or the assay reagent comprises a functional moiety configured to bind to the reactive moiety.

20. The microfluidic device of claim 19 , wherein the functional moiety comprises, in correspondence to the reactive moiety, an antibody, an antigen, a biotin, a streptavidin, an avidin, an alkynyl moiety, an azido moiety, a chelating moiety, an oligonucleotide hybridization sequence, a cell recognition motif, or a combination thereof.

21. The microfluidic device of claim 19 , wherein the functional moiety comprises N-hydroxysuccinimidyl (NHS).

Assignees

• Berkeley Lights Inc

Inventors

• Beaumont Kristin G
• Beemiller Peter J
• Kurz Volker L S
• Lavieu Gregory G
• Wang Xiaohua
• Karunakaran Aathavan

Classifications

• B01L2400/0427

  Electrowetting · CPC title

• B01L2300/0864

  comprising only one inlet and multiple receiving wells, e.g. for separation, splitting · CPC title

• B01L2300/0681

  Filter · CPC title

• B01L2200/0668

  Trapping microscopic beads · CPC title

• B01L3/502792

  for moving individual droplets on a plate, e.g. by locally altering surface tension · CPC title