Compartmentalised combinatorial chemistry by microfluidic control

Patent metadata

Field	Value
Publication number	US-9925504-B2
Application number	US-64315106-A
Country	US
Kind code	B2
Filing date	Dec 20, 2006
Priority date	Mar 31, 2004
Publication date	Mar 27, 2018
Grant date	Mar 27, 2018

Abstract

The invention describes a method for the synthesis of compounds comprising the steps of: (a) compartmentalizing two or more sets of primary compounds into microcapsules; such that a proportion of the microcapsules contains two or more compounds; and (b) forming secondary compounds in the microcapsules by chemical reactions between primary compounds from different sets; wherein one or both of steps (a) and (b) is performed under microfluidic control; preferably electronic microfluidic control The invention further allows for the identification of compounds which bind to a target component of a biochemical system or modulate the activity of the target, and which is co-compartmentalized into the microcapsules.

First claim

We claim:

1. A method comprising:
providing at least a first aqueous fluid comprising at least a first compound,
providing at least a second aqueous fluid comprising at least a second compound,
encapsulating said at least first compound into at least a first aqueous microcapsule within an immiscible oil that comprises a surfactant within a first channel of a microfluidic device,
encapsulating said at least second compound into at least a second aqueous microcapsule within an immiscible oil that comprises a surfactant within a second channel of the microfluidic device,
applying an electric field at a junction of the first channel and the second channel to fuse said at least first and said at least second aqueous microcapsules to form a fused aqueous microcapsule within a third channel of the microfluidic device, thereby causing a chemical reaction between the at least first and at least second compounds to form a fluorogenic reaction product within said fused aqueous microcapsule, and
monitoring for the fluorogenic reaction product by flowing the fused aqueous microcapsule past a detection module that comprises a light source coupled to an optical path used to deliver excitation light to the fused aqueous microcapsule as it passes over the optical path, wherein a plurality of wavelengths of emitted fluorescent light each associated with a different fluorogenic reaction product is collected by the same optical path and the fluorescent light is directed to one or more detectors to measure intensity of each of the wavelengths of the emitted fluorescent light.

2. The method of claim 1 , further comprising isolating said fluorogenic reaction product.

3. The method of claim 2 , wherein said isolating comprises sorting said fused aqueous microcapsule, comprising said fluorogenic reaction product, within an electric field within a channel of a microfluidic device.

4. The method of claim 1 , further comprising identifying said at least first and at least second compounds which reacted to form said fluorogenic reaction product.

5. The method of claim 1 , wherein said at least first compound is attached to a microbead.

6. The method of claim 1 , wherein said at least second compound is attached to a microbead.

7. The method of claim 1 , wherein said at least first compound comprises at least a first label and said at least second compound comprises at least a second label, wherein said at least first and said at least second labels are different.

8. The method of claim 1 , wherein said at least first aqueous microcapsule comprises no more than one said at least first compound.

9. The method of claim 1 , wherein said at least first aqueous microcapsule comprises a plurality of said at least first compounds.

10. The method of claim 1 , wherein said at least second aqueous microcapsule comprises no more than one said at least second compound.

11. The method of claim 1 , wherein said at least second aqueous microcapsule comprises a plurality of said at least second compounds.

12. The method according to claim 1 , wherein the light source is a laser.

13. The method according to claim 1 , wherein the optical path comprises an optical fiber.

14. The method according to claim 1 , wherein the fluorescent light is directed to the one or more detectors by dichroic beam splitters.

15. The method according to claim 1 , wherein the one or more detectors are one or more photomultiplier tubes.

16. The method according to claim 1 , wherein the first compound and the second compound are independently nucleic acids.

17. The method according to claim 1 , wherein the first compound and the second compound are independently RNA or DNA.

Assignees

• Griffiths Andrew
• Weitz David
• Ahn Keunho
• Link Darren
• Bibette Jerome
• Harvard College
• Medical Res Council

Inventors

• Griffiths Andrew
• Weitz David
• Ahn Keunho
• Link Darren
• Bibette Jerome

Classifications

• B01J2219/00576

  fluorophore · CPC title

• B01J2219/00585

  Parallel processes · CPC title

• B01J19/0046 Primary

  Sequential or parallel reactions, e.g. for the synthesis of polypeptides or polynucleotides; Apparatus and devices for combinatorial chemistry or for making molecular arrays (synthesis methods per se C40B50/00) · CPC title

• B01L3/502761

  specially adapted for handling suspended solids or molecules independently from the bulk fluid flow, e.g. for trapping or sorting beads or physically stretching molecules · CPC title

• B82Y10/00

  Nanotechnology for information processing, storage or transmission, e.g. quantum computing or single electron logic · CPC title