IP Library Granted Patent US 10,131,903
Granted Patent B2
US 10,131,903 · App. 13/437,727 · Granted Nov 20, 2018

Microfluidic platform for synthetic biology applications

Inventors: Chieh Chang (San Jose, CA); Rajiv Bharadwaj (Emeryville, CA); Anup K. Singh (Danville, CA); Aarthi Chandrasekaran (San Jose, CA); Nathan J. Hillson (San Francisco, CA)
Assignees: The Regents of the University of California; Sandia Corporation
C12N15/1027C12N15/10C12N15/66
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,131,903
App. No.
13/437,727
Granted
Nov 20, 2018
Kind
B2
Abstract

This invention provides methods and compositions for assembling biological constructs (e.g., plasmids, transformed cells, etc.). In certain embodiments the methods involve encapsulating separate components of the biological construct each in a fluid droplet confined in a fluid channel; optionally mixing droplets from different fluid channels to form a sequenced order of droplets carrying different components of the biological construct in a channel or chamber; and optionally combining two or more droplets each containing different components of the biological construct to permit the components to react with each other in one or more reactions contributing to the assembly of the biological construct.

Claims (16)

1. A method of assembling a biological construct, said method comprising:

encapsulating a plurality of separate components of said biological construct in discrete and separate fluid droplets to provide different components of said construct each in different discrete fluid droplets, where said discrete fluid droplets are disposed in an immiscible fluid that separates said droplets, where a plurality of discrete fluid droplets containing the same type of component are in a single fluid channel containing said immiscible fluid and a plurality of single fluid channels are disposed in a microfluidics device to provide a microfluidics device comprising different fluid channels where each fluid channel contains a plurality of discrete fluid droplets each containing the same type of component and the fluid droplets in different fluid channels contain different components;

introducing fluid droplets from said different fluid channels of said device into a common channel of said device in fluid communication with said plurality of fluid channels to form a spatially sequenced order of separate discrete fluid droplets in an immiscible fluid inside said common channel where different droplets comprising said spatially sequenced order of discrete fluid droplets contain said different components; and

moving the immiscible fluid containing said separate discrete fluid droplets along said common channel and into a droplet merging channel in fluid communication with said common channel to combine two or more fluid droplets of said spatially sequenced order of fluid droplets into a common droplet in said immiscible fluid and to react said separate components with each other in one or more reactions that assemble said separate components together to form said biological construct.

2. The method of claim 1 , wherein said separate components of said biological construct comprise components independently selected from the group consisting of a promoter, a terminator, a secretion signal, a gene, a vector, and a cell.

3. The method of claim 2 , wherein said separate components each contain an element independently selected from the group consisting of a promoter, a terminator, a secretion signal, a gene, and a vector, and said combining two or more fluid droplets of said sequenced order of fluid droplets to react said separate components with each other comprises combining two or more fluid droplets wherein at least one of said fluid droplets further contains a restriction enzyme whereby said combining performs a restriction digest reaction in the combined fluid droplets.

4. The method of claim 1 , wherein said separate components of said biological construct comprise genes and different fluid droplets comprising said sequenced order of fluid droplets contain different genes.

5. The method of claim 4 , wherein said combining two or more fluid droplets of said sequenced order of fluid droplets to react said separate components with each other comprises combining two or more fluid droplets wherein at least one of said two or more fluid droplets further contains a ligase whereby said combining performs a ligation of said different genes to each other in the combined fluid droplets.

6. The method of claim 1 , wherein said combining two or more fluid droplets of said sequenced order of fluid droplets to react said separate components with each other comprises combining two or more fluid droplets wherein at least one of said two or more fluid droplets further contains a ligase whereby said combining performs a ligation of a plurality of genes together under the control of a promoter in the combined fluid droplets.

7. The method of claim 1 , wherein said combining two or more fluid droplets of said sequenced order of fluid droplets to react said separate components with each other comprises combining two or more fluid droplets, wherein at least one of said two or more fluid droplets further contains a vector and said combining introduces said components into said vector.

8. The method of claim 7 , wherein said vector is a plasmid or cosmid.

9. The method of claim 1 , wherein said combining two or more fluid droplets of said sequenced order of fluid droplets to react said separate components with each other comprises combining two or more fluid droplets to assemble a nucleic acid construct using constructs selected from the group consisting of DNA sequences that conform to a restriction-enzyme assembly standard, constructs for sequence and ligation independent cloning (SLIC), constructs configured for the joining of multiple DNA fragments in a single, isothermal reaction, constructs for circular polymerase extension cloning (CPEC), and constructs incorporating a recognition site for a single type IIS restriction enzyme and a T4 DNA ligase.

10. The method of claim 1 , wherein said combining two or more fluid droplets of said sequenced order of fluid droplets to react said separate components with each other comprises combining two or more fluid droplets, wherein at least one of said two or more fluid droplets further contains a cell and said combining introduces a nucleic acid construct into said cell.

11. The method of claim 10 , wherein said cell is selected from the group consisting of a bacterial cell, a mammalian cell, an insect cell, a plant cell, an algal cell, and a fungal cell.

12. The method of claim 10 , wherein said method further comprises identifying and capturing and/or trapping a cell containing said construct.

13. The method of claim 1 , wherein said immiscible fluid comprises an oil.

Assignments (4)
CONFIRMATORY LICENSE Recorded Aug 20, 2019
From: UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB
To: UNITED STATES DEPARTMENT OF ENERGY
Reel/Frame 050104/0318 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 7, 2012
From: CHANG, CHIEH; BHARADWAJ, RAJIV; SINGH, ANUP K.; CHANDRASEKARAN, AARTHI
To: SANDIA CORPORATION
Reel/Frame 028338/0037 →
CONFIRMATORY LICENSE Recorded May 21, 2012
From: RGENTS OF THE UNIVERSITY OF CALIFORNIA, THE
To: UNITED STATE DEPARTMENT OF ENERGY
Reel/Frame 028254/0286 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 13, 2012
From: HILLSON, NATHAN J.
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 028046/0085 →
Continuity (2)
Provisional Application 61471027 · Apr 1, 2011
Related Publication 20120258487A1 · Oct 11, 2012