MICROFLUIDIC DROPLETS FOR METABOLIC ENGINEERING AND OTHER APPLICATIONS

• US 20100124759A1
• Filed: 06/26/2009
• Published: 05/20/2010
• Est. Priority Date: 06/27/2008
• Status: Abandoned Application

• Current Assignee: President and Fellows of Harvard College (Harvard Corporation), Massachusetts Institute of Technology
• Original Assignee: President and Fellows of Harvard College (Harvard Corporation), Massachusetts Institute of Technology
• Inventors: Humphry, Katherine J., Wang, Benjamin L., Weitz, David A., Stephanopoulos, Gregory
• Application Number:
  US12/492,830
• Publication Number:
  US 20100124759A1
• Time in Patent Office: Days
• US Class Current: 435/28
• CPC Class Codes: B01L 2200/0647 Handling flowable solids, e.g. microscopic beads, cells, particles
• CPC Class Codes: B01L 2200/0652 Sorting or classification of particles or molecules
• CPC Class Codes: B01L 2200/10 Integrating sample preparation and analysis in single entity, e.g. lab-on-a-chip concept
• CPC Class Codes: B01L 2300/0681 Filter
• CPC Class Codes: B01L 2300/0816 Cards, e.g. flat sample carriers usually with flow in two horizontal directions
• CPC Class Codes: B01L 2300/087 Multiple sequential chambers
• CPC Class Codes: B01L 2400/0421 electrophoretic flow
• CPC Class Codes: B01L 3/502715 characterised by interfacing components, e.g. fluidic, electrical, optical or mechanical interfaces
• CPC Class Codes: B01L 3/502753 characterised by bulk separation arrangements on lab-on-a-chip devices, e.g. for filtration or centrifugation separation in general B01D; microapparatus for analysis using electrophoresis G01N27/44791; sample preparation G01N1/28
• CPC Class Codes: B01L 3/502761 specially adapted for handling suspended solids or molecules independently from the bulk fluid flow, e.g. for trapping or sorting beads, for physically stretching molecules investigating characteristics of particles G01N15/00

Abstract

The present invention relates generally to the use of droplets to culture and/or assay cells or other species. In some cases, the cells or other species may be sorted based upon the results of the culture and/or assay. In some embodiments, cells other species can be encapsulated in droplets and exposed to one or more agents (e.g., a sugar, an indicator dye, etc.). For instance, in some cases, exposure of cells to the agents may result in the production of metabolites or other compounds (e.g., amino acids, proteins, organic acids, etc.) which may be, for example, assayed or otherwise determined. In some embodiments, the reaction of an agent with cells and/or other species within a droplet may reveal a property of the cells or other species (e.g., sugar consumption, growth rate, ability to withstand exposure to the agent, etc.). As an example, cells that produce desired metabolites or exhibit certain properties may be separated from the other cells via sorting techniques. Other aspects of the invention relate to devices or kits for implementing such sorts, methods of promoting such techniques, or the like.

Claims

1. A method of producing an enriched population of cells, comprising:

providing a first population of droplets contained within a microfluidic device, at least some of which droplets encapsulate one or more cells, at least some of which droplets include a first cell type and at least some of which droplets include a second cell type;

for at least some of the droplets, determining the ability of one or more cells within the respective droplets to react with a sugar, wherein the first cell type is able to metabolize the sugar to a greater degree than the second cell type; and

based on the determination, producing an enriched population of droplets of cells of the first cell type relative to the second cell type.

2. The method of claim 1, wherein the sugar is xylose.

3. The method of claim 1, wherein the sugar is glucose.

4. The method of claim 1, wherein the amount of enrichment of the first cell type relative to the second cell type is a factor of at least about 10.

5. The method of claim 1, wherein the amount of enrichment of the first cell type relative to the second cell type is a factor of at least about 100.

6. The method of claim 1, wherein the amount of enrichment of the first cell type relative to the second cell type is a factor of at least about 1000.

7. The method of claim 1, wherein the act of producing an enriched population of droplets of cells of the first cell type relative to the second cell type comprises directing at least some of the cells of the first cell type to a first location within the microfluidic device and directing at least some of the cells of the second cell type to a second location within the microfluidic device

8. The method of claim 7, wherein the cells are directed to the first location and/or the second location by applying an electric field to the cells.

9. The method of claim 1, further comprising sequencing DNA of the first cell type.

10. The method of claim 1, wherein the first cell type and the second cell type arise from the same species.

11. The method of claim 1, wherein the first cell type and the second cell type arise from different species.

12. The method of claim 1. wherein the act of determining the ability of the one or more cells within the droplet to react with a sugar comprises determining the ability of the one or more cells to react with the sugar using fluorescence.

13. The method of claim 1, further comprising culturing at least a portion of the enriched population of droplets of cells.

14. A method of producing an enriched population of cells, comprising:

providing a population of droplets contained within a microfluidic device, at least some of which droplets encapsulate one or more cells, at least some of which droplets of the population of droplets include a first cell type and at least some of which droplets include a second cell type;

for at least some of the droplets, determining the ability of one or more cells within the droplet to react with an agent, wherein the first cell type reacts with the agent to a greater degree than does the second cell type; and

based on the determination, producing an enriched population of droplets of cells of the first cell type relative to the second cell type.

15. The method of claim 14, wherein the act of producing an enriched population of droplets of cells of the first cell type relative to the second cell type comprises directing at least some of the cells of the first cell type to a first location within the microfluidic device and directing at least some of the cells of the second cell type to a second location within the microfluidic device

16. The method of claim 15, wherein the cells are directed to the first location and/or the second location by applying an electric field to the cells.

17. The method of claim 14, wherein the agent is a sugar that is metabolized by at least the first cell type.

18. The method of claim 14, wherein the agent is xylose.

19. The method of claim 14, wherein the agent is glucose.

20-36. -36. (canceled)

37. A method, comprising:

providing a population of droplets contained within a microfluidic device, at least some of which droplets encapsulate one or more cells and at least some of which droplets contain a sugar;

exposing at least some of the droplets to an enzyme able to react with the sugar; and

determining an extent of reaction of the enzyme with the sugar.

38-65. -65. (canceled)