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High throughput screening assay systems in microscale fluidic devices    
United States Patent5942443   
Link to this pagehttp://www.wikipatents.com/5942443.html
Inventor(s)Parce; John Wallace (Palo Alto, CA); Kopf-Sill; Anne R. (Portola Valley, CA); Bousse; Luc J. (Menlo Park, CA)
AbstractMicrofluidic devices and methods that are useful for performing high-throughput screening assays. In particular, the devices and methods of the invention are useful in screening large numbers of different compounds for their effects on a variety of chemical, and preferably, biochemical systems.
   














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Patent Text Patent PDF Print Page Summary File History
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Inventor     Parce; John Wallace (Palo Alto, CA); Kopf-Sill; Anne R. (Portola Valley, CA); Bousse; Luc J. (Menlo Park, CA)
Owner/Assignee     Caliper Technologies Corporation (Palo Alto, CA)
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Publication Date     August 24, 1999
Application Number     08/671,987
PAIR File History     Application Data   Transaction History
Image File Wrapper   Patent Term   Fees
Litigation
Filing Date     June 28, 1996
US Classification     436/514 204/451 204/490 204/600 204/601 435/4 435/6
Int'l Classification     G01N 033/558
Examiner     Housel; James C.
Assistant Examiner     Portner; Ginny Allen
Attorney/Law Firm     Crew, Murphy; Matthew B. Townsend and Townsend and Quine; Jonathan , Alan
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Priority Data    
USPTO Field of Search     436/514 435/4 435/6
Patent Tags     high throughput screening assay microscale fluidic devices
   
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5780754
Karlberg
73/864.81
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Lynggaard
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What is claimed is:

1. A method of screening test compounds for an effect on an interaction between components of a biochemical system, comprising;

providing a substrate having at least two intersecting channels disposed therein, at least one of said at least two intersecting channels having at least one cross-sectional dimension in a range from 0.1 to 500 .mu.m;

continuously flowing interacting components of a biochemical system in a first of said at least two intersecting channels;

flowing at least a first test compound from a second channel into said first channel whereby said first flowing test compound contacts said flowing components of said biochemical system; and

detecting an effect of said at least first flowing test compound on interactions between said continuously flowing components of said biochemical system.

2. The method of claim 1, wherein said components of a biochemical system produce a detectable signal representative of a function of said biochemical system.

3. The method of claim 1, wherein said components further comprise an indicator compound which interacts with said components to produce a detectable signal representative of a functioning of said biochemical system.

4. The method of claim 1, wherein components of a biochemical system comprise an enzyme and a substrate for said enzyme, wherein action of said enzyme on said substrate produces a detectable signal.

5. The method of claim 1, wherein said components of a biochemical system comprise a receptor/ligand binding pair, wherein at least one of said receptor or ligand has a detectable signal associated therewith.

6. The method of claim 1, wherein said components of a biochemical system comprise a receptor/ligand binding pair, wherein binding of said receptor to said ligand produces a detectable signal.

7. The method of claim 1, wherein said components of a biochemical system comprise components of cells, which cells are flowing in said first channel, and said detecting step comprises determining an effect of said test compound on said cells.

8. The method of claim 7, wherein said cells are capable of producing a detectable signal corresponding to a cellular function, and said detecting step comprises detecting an effect of said test compound on said cellular function by detecting a level of said detectable signal.

9. The method of claim 7, wherein said detecting step comprises detecting an effect of said test compound on viability of said cells.

10. A method of screening a plurality of test compounds for an effect on a biochemical system, comprising:

providing a substrate having at least two intersecting channels disposed therein, at least one of said at least two intersecting channels having at least one cross-sectional dimension in a range from 0.1 to 500 .mu.m;

continuously flowing interacting components of a biochemical system in a first channel of said at least two intersecting channels;

periodically introducing a different flowing test compound into said first channel from a second channel of said at least two intersecting channels; and

detecting an effect of said test compound on said continuously flowing interacting components of a biochemical system.

11. The method of claim 10, wherein said step of periodically introducing comprises flowing a plurality of different test compounds into said first channel from a second channel of said at least two intersecting channels, each of said plurality of different test compounds being physically isolated from each other of said plurality of different test compounds.

12. The method of claim 10, wherein said components of a biochemical system produce a detectable signal representative of a function of said biochemical system.

13. The method of claim 12, wherein said detecting comprises monitoring said detectable signal from said continuously flowing components at a point on said first channel, said detectable signal having a steady state intensity, and wherein said effect of said interaction between said components and said test compound comprises a deviation from said steady state intensity of said detectable signal.

14. The method of claim 12, wherein said components of a biochemical system comprise an indicator compound which interacts with at least a first component of a biochemical system to produce a detectable signal representative of a functioning of said biochemical system.

15. The method of claim 14, wherein said components of a biochemical system comprises an enzyme and said indicator compound comprises a substrate for said enzyme, wherein action of said enzyme on said substrate produces a detectable signal.

16. The method of claim 12, wherein said components of a biochemical system comprise a receptor/ligand binding pair, wherein at least one of said receptor or ligand has a detectable signal associated therewith.

17. The method of claim 16, wherein said receptor and said ligand flow along said first channel at different rates.

18. The method of claim 12, wherein said components of a biochemical system comprises a receptor/ligand binding pair, wherein binding of said receptor to said ligand produces a detectable signal.

19. The method of claim 10, wherein said components of a biochemical system comprise cells, and said detecting step comprises determining an effect of said test compound on said cells.

20. The method of claim 19, wherein said cells are capable of producing a detectable signal corresponding to a cellular function, and said detecting step comprises detecting an effect of said test compound on said cellular function by detecting a level of said detectable signal.

21. The method of claim 19, wherein said detecting step comprise s detecting an effect of said test compound on viability of said cells.

22. A method of screening a plurality of different test compounds for an effect on a biochemical system, comprising:

providing a substrate having at least a first surface, and a plurality of reaction channels fabricated in said first surface, each of said plurality of reaction channels being fluidly connected to at least two transverse channels fabricated in said surface;

introducing components of a biochemical system into said plurality of reaction channels;

flowing a plurality of different test compounds through at least one of said at least two transverse channels, each of said plurality of test compounds being introduced into said at least one transverse channels in a discrete volume;

directing each of said plurality of different test compounds into a separate one of said plurality of reaction channels; and

detecting an effect of each of said test compounds on said components of said biochemical system.

23. The method of claim 22, wherein said components of said biochemical system produce a flowable detectable signal representative of a function of said biochemical system.

24. The method of claim 23, wherein said detectable flowable signal produced in each of said plurality of reaction channels is flowed into and through said second transverse channel, each of said detectable flowable signals produced in each of said plurality of reaction channels being physically isolated from each other of said detectable flowable signals, whereupon each of said detectable flowable signals is separately detected.

25. The method of claim 23, wherein said flowable signal comprises a soluble signal.

26. The method of claim 25, wherein said soluble signal is selected from fluorescent or colorimetric signals.

27. The method of claim 22, wherein said components comprise an indicator compound which interacts with at least a first component of a biochemical system to produce a detectable signal representative of a functioning of said biochemical system.

28. The method of claim 27, wherein said first component of a biochemical system comprises an enzyme and said indicator compound comprises a substrate for said enzyme, wherein action of said enzyme on said substrate produces a detectable signal.

29. The method of claim 22, wherein said components of a biochemical system comprise a receptor/ligand binding pair, wherein at least one of said receptor or ligand has a detectable signal associated therewith.

30. The method of claim 22, wherein said components of a biochemical system comprise a receptor/ligand binding pair, wherein binding of said receptor to said ligand produces a detectable signal.

31. The method of claim 22, wherein said components of a biochemical system comprise cells, and said detecting step comprises determining an effect of said test compound on said cells.

32. The method of claim 31, wherein said cells are capable of producing a detectable signal corresponding to a cellular function, and said detecting step comprises detecting an effect of said test compound on said cellular function by detecting a level of said detectable signal.

33. The method of claim 32, wherein said detecting step comprises detecting an effect of said test compound on viability of said cells.

34. The method of claim 22, wherein each of said plurality of different test compounds is immobilized upon a separate bead, and said step of directing each of said plurality of different test compounds into a separate one of said plurality of reaction channels comprises:

lodging one of said separate beads at an intersection of said first transverse channel and each of said plurality of reaction channels; and

controllably releasing said test compounds from each of said separate beads into each of said plurality of reaction channels.

35. The method of claim 1, wherein said components and said first test compound are flowed electroosmotically.

36. The method of claim 1, wherein said electrokinetic fluid direction system is used for flowing said components within said first channel and for introducing said test compound from said second channel to said first channel.

37. The method of claim 36, further comprising generating a continuous flow of a fluid mixture comprising said components, and periodically injecting the first test compound from said second channel in to the continuous flow of the fluid mixture in said first channels.

38. The method of claim 1 wherein said components and said test compound are flowed by concomitantly applying a variable voltage to at least three electrodes in electrical contact with said at least two intersecting channels.

39. The method of claim 10, wherein said components and said different test compounds are flowed electroosmotically.

40. The method of claim 10, wherein an electrokinetic fluid direction system is used for flowing said components within said first channel and for introducing said different test compound from said second channel to said first channel.

41. The method of claim 40, further comprising generating a continuous flow of a fluid mixture comprising said components, and periodically injecting the different test compound from said second channel into the continuous flow of the fluid mixture in said first channel.

42. The method of claim 10, wherein said components and said test compound are flowed by concomitantly applying a variable voltage to at least three electrodes in electrical contact with said at least two intersecting channels.

43. The method of claim 22, wherein said components and said plurality of different test compound are flowed electroosmotically.

44. The method of claim 22, wherein an electrokinetic fluid direction system is used for flowing said components within said first channel and for introducing said plurality of test compounds from said second channel to said first channel.

45. The method of claim 44, further comprising generating a continuous flow of a fluid mixture of said components along said first channel, and periodically injecting a one or more of the plurality of test compounds from said second channel into the fluid mixture in said first channel.

46. The method of claim 22, wherein said components and said plurality of test compounds are flowed by concomitantly applying a variable voltage to at least three electrodes in electrical contact with said at least two intersecting channels.

47. A method of screening a plurality of test compounds for an effect on a biochemical system, comprising:

providing a first channel and a second channel which intersect, wherein at least one of said first and second channels has a cross sectional dimension in the range from 0.1 to 500 .mu.m;

continuously flowing interacting components of the biochemical system into said first channel;

introducing at least a first flowing test compound into the first channel from the second channel; and

detecting an effect of the first flowing test compound on an interaction between the continuously flowing components of the biochemical system.

48. The method of claim 47 further comprising providing a detection zone in said first or said second channel.

49. The method of claim 47, wherein the components comprise a component of a receptor/ligand binding pair.

50. The method of claim 47, wherein the components are selected from an enzyme, an enzyme substrate, and a biological cell.

51. The method of claim 47, wherein detecting the effect of the first test compound on the biochemical system comprises monitoring a fluorescent signal.

52. The method of claim 47, further comprising flowing a second component of the biochemical system into said first channel.

53. The method of claim 47, further comprising flowing a second test compound into said first channel.

54. The method of claim 47, further comprising flowing a second test compound into said first channel, wherein the first test compound and the second test compound are not mixed.

55. The method of claim 47, wherein said components and said first test compound are flowed electroosmotically.

56. The method of claim 47, wherein an electrokinetic fluid direction system is used for flowing said components within said first channel and for introducing said test compound from said second channel to said first channel.

57. The method of claim 56, further comprising generating a continuous flow of a fluid mixture comprising said components along the first ch