Microparticle based biochip systems and uses thereof

• US 20070184433A1
• Filed: 07/14/2003
• Published: 08/09/2007
• Est. Priority Date: 05/19/2003
• Status: Abandoned Application

• Current Assignee: CapitalBio Corporation, Tsinghua University
• Original Assignee: CapitalBio Corporation, Tsinghua University
• Inventors: Wang, Guoqing, Cheng, Jing, Tao, Shengce
• Application Number:
  US10/557,328
• Publication Number:
  US 20070184433A1
• Time in Patent Office: Days
• US Class Current: 435/5
• CPC Class Codes: B01L 2200/0647 Handling flowable solids, e.g. microscopic beads, cells, particles
• CPC Class Codes: B01L 2300/0636 Integrated biosensor, microarrays
• CPC Class Codes: B01L 2300/0819 Microarrays; Biochips
• CPC Class Codes: B01L 2400/0409 centrifugal forces
• CPC Class Codes: B01L 2400/0415 electrical forces, e.g. electrokinetic
• CPC Class Codes: B01L 2400/043 magnetic forces
• CPC Class Codes: B01L 3/508 rigid containers not provided for above
• CPC Class Codes: C12Q 1/6834 Enzymatic or biochemical coupling of nucleic acids to a solid phase
• CPC Class Codes: C12Q 1/689 for bacteria
• CPC Class Codes: C12Q 1/706 for hepatitis
• CPC Class Codes: C12Q 2563/143 Magnetism, e.g. magnetic label
• CPC Class Codes: C12Q 2563/149 Particles, e.g. beads
• CPC Class Codes: G01N 33/552 Glass or silica
• CPC Class Codes: G01N 33/558 using diffusion or migration of antigen or antibody immunochromatographic test strips G01N33/54387

Abstract

This invention relates generally to the field of analyte assays. In particular, the invention provides a device for analyzing an analyte, which device comprises, inter alia, various means for moving analytes and other items to facilitate binding between analytes and their binding reagents immobilized on a surface and to facilitate clearance of undesirable items away from analyte-binding reagent interaction area to reduce background noise in the assay. Methods for analyzing an analyte using the devices are also disclosed.

Claims

1. A device for analyzing an analyte, which device comprises:

a) a controllably closed space enclosed by a suitable material on a substrate, wherein said suitable material is thermoconductive, biocompatible and does not inhibit binding between an analyte and a reactant, and said controllably closed space comprising, on the surface of said substrate, a first immobilized reactant capable of binding to said analyte;

b) a first means for controllably moving said analyte to said first immobilized reactant;

c) a second means for controllably moving said analyte to a labeled unimmobilized complex comprising a second reactant capable of binding to said analyte and a microparticle; and

d) a third means for controllably moving said labeled unimmobilized complex unbound to said analyte away from said first immobilized reactant,

and wherein addition of a sample comprising said analyte and said labeled unimmobilized complex into said controllably closed space and operation of said means result in formation of a sandwich of said labeled unimmobilized complex-said analyte-said first immobilized reactant on said substrate.

2. The device of claim 1, wherein the suitable material is a self seal chamber, a self seal gel or a plastic chamber.

3. The device of claim 1, wherein the substrate comprises a material selected from the group consisting of a silicon, a plastic, a glass, a quartz glass, a ceramic, a rubber, a metal, a polymer, a hybridization membrane, and a combination thereof.

4. The device of claim 1, wherein the surface of the substrate is modified to contain a chemically reactive group or a biomolecule.

5. The device of claim 4, wherein the chemically reactive group is selected from the group consisting of —

CHO, —

NH₂, —

SH, —

S—

S—

, an epoxy group and a Tosyl group.

6. The device of claim 4, wherein the biomolecule is selected from the group consisting of biotin, streptavidin, avidin, his-tag, strept-tag, histidine tag and protein A.

7. The device of claim 1, wherein the analyte is selected from the group consisting of a cell, a cellular organelle, a virus, a molecule and an aggregate or complex thereof.

8. The device of claim 1, wherein the first immobilized reactant is selected from the group consisting of a cell, a cellular organelle, a virus, a molecule and an aggregate or complex thereof.

9. The device of claim 1, wherein the first immobilized reactant specifically binds to the analyte.

10. The device of claim 1, wherein the first immobilized reactant is immobilized on the substrate via a chemically reactive group or a biomolecule contained on the surface of the substrate.

11. The device of claim 1, wherein the labeled unimmobilized complex comprises a detectable label on the second reactant or on the microparticle.

12. The device of claim 11, wherein the detectable label is selected from the group consisting of a radioactive label, a fluorescent label, a chemical label, an enzymatic label, a luminescent label, a fluorescence resonance energy transfer (FRET) label and a molecular beacon.

13. The device of claim 11, wherein the detectable label is a fluorescent label.

14. The device of claim 13, wherein the fluorescent label is adjacent to a second fluorescent label to generate the fluorescent signal.

15. The device of claim 13, wherein the fluorescent label is selected from the group consisting of FAM, TET, HEX, FITC, Cy3, Cy5, Texas Red, ROX, Fluroscein, TAMRA and a nanoparticle comprising a rare-earth metal.

16. The device of claim 1, wherein the second reactant is selected from the group consisting of a cell, a cellular organelle, a virus, a molecule and an aggregate or complex thereof.

17. The device of claim 1, wherein the second reactant specifically binds to the analyte.

18. The device of claim 1, wherein the second reactant is conjugated to the microparticle via a chemically reactive group or a biomolecule contained on the surface of the microparticle.

19. The device of claim 18, wherein the chemically reactive group is selected from the group consisting of —

CHO, —

NH₂, —

SH, —

S—

S—

, an epoxy group and a Tosyl group.

20. The device of claim 18, wherein the biomolecule is selected from the group consisting of biotin, streptavidin, avidin, his-tag, strept-tag, histidine tag and protein A.

21. The device of claim 1, wherein the microparticle is a magnetic, a magnetizable, an electrically charged or an electrically chargeable microparticle.

22. The device of claim 1, wherein the microparticle comprises a material selected from the group consisting of an organic material, a glass, a SiO₂, a ceramic, a carbon and a metal.

23. The device of claim 1, wherein the microparticle has a diameter ranging from about 1 nm to about 20 μ

m.

24. The device of claim 1, wherein the first means controllably moves the analyte to the first immobilized reactant via a force selected from the group consisting of electric, magnetic, acoustic, gravitational and centrifugational force.

25. The device of claim 1, wherein the second means controllably moves the analyte to the labeled unimmobilized complex via a force selected from the group consisting of electric, magnetic, acoustic, gravitational and centrifugational force.

26. The device of claim 25, wherein the second means controllably moves the analyte to the labeled unimmobilized complex by exerting a force on the microparticle of the labeled unimmobilized complex.

27. The device of claim 1, wherein the third means controllably moves the labeled unimmobilized complex unbound to the analyte away from the first immobilized reactant via a force selected from the group consisting of electric, magnetic, acoustic, gravitational and centrifugational force.

28. The device of claim 27, wherein the third means controllably moves the labeled unimmobilized complex unbound to the analyte away from the first immobilized reactant by exerting a force on the microparticle of the labeled unimmobilized complex.

29. The device of claim 1, wherein the analyte is selected from the group consisting of a DNA, a RNA, a peptide nucleic acid (PNA), a locked nucleic acid (LNA), a protein, a peptide, an antibody and a polysaccharide.

30. The device of claim 29, wherein the DNA, RNA, PNA and LNA has a length ranging from about 5 basepairs to about 1,000 basepairs.

31. The device of claim 1, which is used to analyze DNA-DNA hybridization, DNA-RNA hybridization, DNA-LNA hybridization, DNA-PNA hybridization, RNA-RNA hybridization, RNA-PNA hybridization, RNA-LNA hybridization, PNA-PNA hybridization, PNA-LNA hybridization, protein-protein interaction, protein-nucleic-acid interaction, protein-polysaccharide interaction or antigen-antibody interaction.

32. The device of claim 1, which comprises a single or multiple analytic paths.

33. The device of claim 1, which comprises from about 1 to about 10,000 analytic paths.

34. The device of claim 1, which further comprises a temperature control means.

35. The device of claim 34, wherein the temperature control means comprises a PCR machine, an in situ PCR thermal cycler, a water bath or a micro thermal-controller.

36. The device of claim 1, which further comprises a means for detecting the sandwich of the labeled unimmobilized complex-the analyte-the first immobilized reactant.

37. The device of claim 36, wherein the detecting means comprises a microscope, an optical scanner or fluorescent scanner.

38. The device of claim 1, wherein the sandwich of the labeled unimmobilized complex-the analyte-the first immobilized reactant on the substrate without any material exchange between said controllably closed space and the outside environment.

39. A method for analyzing an analyte, which method comprises:

a) providing a device of claim 1;

b) introducing a sample containing or suspected of containing an analyte and a labeled unimmobilized complex comprising a second reactant capable of binding to said analyte and a microparticle into said controllably closed space of said device;

c) operating said means of said device to form a sandwich of said labeled unimmobilized complex-said analyte-said first immobilized reactant on said substrate;

d) assessing said sandwich to determine presence and/or quantity of said analyte in said sample.

40. The method of claim 39, wherein the sample is a solid, liquid or gas sample.

41. The method of claim 39, which is used to analyze a single or multiple analytes.

42. The method of claim 41, wherein the multiple analytes are analyzed sequentially or simultaneously.

43. The method of claim 39, which is used to analyze from about 1 to about 30,000 analytes.

44. The method of claim 39, wherein the sandwich of the labeled unimmobilized complex-the analyte-the first immobilized reactant is formed by first moving the analyte to the labeled unimmobilized complex using the second means, allowing the analyte to bind to the labeled unimmobilized complex, and then moving the bound analyte-labeled unimmobilized complex to the first immobilized reactant using the first means, allowing the bound analyte-labeled unimmobilized complex to bind to the first immobilized reactant to form the sandwich, and controllably moving the labeled unimmobilized complex unbound to the analyte away from the first immobilized reactant using the third means.

45. The method of claim 39, wherein the microparticle in the labeled unimmobilized complex itself functions as a directly detectable label.

46. The method of claim 39, wherein the sandwich of the labeled unimmobilized complex-the analyte-the first immobilized reactant on the substrate without any material exchange between said controllably closed space and the outside environment.