Microdevices for high-throughput screening of biomolecules

• US 6,582,969 B1
• Filed: 05/12/2000
• Issued: 06/24/2003
• Est. Priority Date: 07/14/1998
• Status: Expired due to Fees

• Current Assignee: Zyomyx, Inc.
• Original Assignee: Zyomyx, Inc.
• Inventors: Wagner, Peter, Itin, Christian, Nock, Steffen, Ault-Riche, Dana
• Primary Examiner(s): Chin, Christopher L.
• Application Number:
  US09/570,586
• Time in Patent Office: 1,138 Days
• Field of Search: 436/501, 436/514, 436/518, 436/524-535, 435/4, 435/6, 435/7.1, 435/287.1, 435/287.2, 435/805, 435/810, 422/50, 422/58, 422/100
• US Class Current: 436/518
• CPC Class Codes: B82Y 30/00 Nanotechnology for materials or surface science, e.g. nanocomposites
• CPC Class Codes: C12Q 1/37 involving peptidase or proteinase
• CPC Class Codes: C12Q 1/70 involving virus or bacteriophage immunoassay for viruses G01N33/56983
• CPC Class Codes: Y10S 435/805 Test papers
• CPC Class Codes: Y10S 435/81 Packaged device or kit
• CPC Class Codes: Y10T 436/143333 Saccharide [e.g., DNA, etc.]

Abstract

Methods for the parallel, in vitro screening of biomolecular activity using miniaturized microfabricated devices are provided. The biomolecules that can be immobilized on the surface of the devices of the present invention include proteins, polypeptides, nucleic acids, polysaccharides, phospholipids, and related unnatural plyomers of biological relevance. These devices are useful in high-throughput drug screening and clinical diagnostics and are preferably used for the parallel screening of families of related proteins.

Claims

1. A method of screening a plurality of immobilized biological moieties for their ability to interact with one or more components of a fluid sample comprising the steps of:

(i) providing a multi-channel sample detection device, said sample detection device comprising;

(a) a substrate having an upper surface,

(b) a plurality of discrete open channels formed in or on said substrate adjacent said upper surface, each channel extending between first and second ends and having a bottom wall surface defining an immobilization region intermediate said first and second ends,

(c) a cover attached to said substrate'"'"'s upper surface and forming with each channel a closed channel having open first and second ends, said cover being part of a detection system for detecting interactions between said biological moieties and said components of said fluid sample within each channel,

(d) one or more of said biological moieties for immobilizing said components of said fluid sample, said biological agents being immobilized by being chemisorbed or physisorbed to said immobilization regions in each channel to form immobilized biological moieties,

wherein when said fluid containing said components is introduced into said channels to interact with said immobilized biological moieties, such interactions, if any, can be detected by said detection device;

(ii) contacting said fluid with at least one of said channels so that said fluid contacts said immobilized biological moieties within said channel; and

,

(iii) monitoring said interactions, if any, between said immobilized biological moieties and said components of said fluid.

2. The method of claim 1, wherein at least one of said open ends is formed by said cover and said upper surface of said substrate.

3. The method of claim 1, wherein at least one of said channels has a cross-section that is between about 10 μ

m and 500 μ

m, and a length between about 1 to 20 mm.

4. The method of claim 1, wherein said cover is non-translucent or non-transparent.

5. The method of claim 1, wherein said cover is translucent or transparent.

6. The method of claim 1, wherein said immobilization region in at least one of said microchannels is oriented parallel to at least one other immobilization region in one other microchannel in said device.

7. The method of claim 1, wherein said immobilized biological moieties are chemisorbed or physisorbed to said immobilization regions through an X-RY monolayer.

8. The method of claim 1, further comprising a coating disposed between said bottom wall surface within said immobilization regions and said immobilized biological moieties within such immobilization regions.

9. The method of claim 1, wherein said immobilized biological moieties are chemisorbed or physisorbed to said immobilization regions through a lipid bilayer.

10. The method of claim 1, wherein said interaction produces a product and said detector detects said product.