Capture and release assay system and method

• US 20060211055A1
• Filed: 05/24/2006
• Published: 09/21/2006
• Est. Priority Date: 11/12/2002
• Status: Abandoned Application

• Current Assignee: Caliper Life Sciences Incorporated (Revvity, Inc.)
• Original Assignee: Caliper Life Sciences Incorporated (Revvity, Inc.)
• Inventors: Simeonov, Anton, Wada, H. Garrett, Hafeman, Dean G.
• Application Number:
  US11/440,615
• Publication Number:
  US 20060211055A1
• Time in Patent Office: Days
• US Class Current: 435/7.500
• CPC Class Codes: G01N 33/54306 Solid-phase reaction mechanisms

Abstract

A method for detecting one or more components of interest in a fluid-borne sample in a microchannel of a microfluidic device includes flowing the fluid-borne sample, in which the one or more components of interest are bound to a first labeled component binding moiety to form a first labeled complex, through a binding channel region of the microchannel. The binding channel region includes a second component-binding moiety reversibly bound to a wall surface of the binding channel region. At least a portion of the one or more components of interest is bound to the second component-binding moiety to form a second labeled complex. The second labeled complex is released from the binding channel region and flowed through a detection channel region of the microchannel, where the second labeled complex is detected.

Claims

1. A method for detecting one or more component of interest in a fluid-borne sample in a microchannel of a microfluidic device, the method comprising the steps of:

(i) flowing the fluid-borne sample comprising the one or more component of interest bound to a first labeled component binding moiety to form a first labeled complex through a binding channel region of the microchannel, which binding channel region comprises at least a second component-binding moiety that is reversibly bound to a wall surface of the binding channel region, thereby binding at least a portion of the one or more components of interest to the second component-binding moiety to form a second labeled complex;

(iii) releasing the second labeled complex comprising the first and second component binding moieties and the one or more component of interest from the binding channel region, thereby releasing the second labeled complex into the microchannel; and

,

(iv) flowing the released second labeled complex through a detection channel region of the microchannel and detecting the second labeled complex.

2. The method of claim 1, wherein the protein comprises alpha-fetoprotein.

3. The method of claim 2, wherein the first and second component-binding moieties comprise antibodies specific to the alpha-fetoprotein.

4. The method of claim 3, wherein one of the antibodies comprises a nucleic acid chain bound thereto which includes at least one fluorescent label associated therewith.

5. The method of claim 4, wherein the nucleic acid chain bound to the antibody comprises two or more fluorescent labels.

6. The method of claim 1, wherein the wall surface of the binding channel region of the microchannel is at least partially coated with biotin derivatized silane to which streptavidin is bound, wherein the streptavidin is used to bind a biotinylated nickel chelator that binds nickel to the wall surface of the binding channel region of the microchannel.

7. The method of claim 6, wherein the first component binding moiety is coupled to a polyhistidine tail to mediate binding to the nickel coated wall surface of the binding channel region of the microchannel.

8. The method of claim 7, wherein the step of releasing the second complex from the binding channel region comprises flowing an elution buffer through the microchannel.

9. The method of claim 8, wherein the elution buffer comprises imidazole buffer.

10. The method of claim 1, wherein the first component-binding moiety comprises at least one detectable label moiety.

11. The method of claim 10, wherein the first component binding moiety further comprises a charge modifying moiety.

12. The method of claim 11, wherein the charge modifying moiety comprises a nucleic acid chain.

13. The method of claim 12, wherein the nucleic acid chain is bound to the at least one label moiety.

14. The method of claim 1, wherein the binding channel region comprises a derivatized channel.

15. The method of claim 1, wherein the binding channel region comprises one or more particle set, the particle set comprising a plurality of particle member types.

16. The method of claim 1, wherein flowing the fluid-borne sample through the binding channel region comprises applying pressure to the fluid in the microchannel.

17. The method of claim 1, wherein flowing the fluid-borne sample through the binding channel region comprises electrokinetically flowing the fluid therein.

18. The method of claim 1, wherein releasing the second complex from the binding channel region comprises adjusting the temperature or pH in the binding channel region or introducing one or more releasing reagents into the binding channel region.

19. The method of claim 1, wherein detecting the released second complex comprises optically detecting a fluorescent label moiety fixed to one or more of the component of interest or the first component binding moiety.

20. The method of claim 1, further comprising labeling the first component binding moiety with a fluorescent label and detecting the released second complex by detecting the fluorescent label.

21. The method of claim 1, wherein the second component binding moiety is unlabeled.