Large scale parallel immuno-based allergy test and device for evanescent field excitation of fluorescence

• US 20070117217A1
• Filed: 06/09/2006
• Published: 05/24/2007
• Est. Priority Date: 06/16/2005
• Status: Abandoned Application

• Current Assignee: Regents of the University of California (University of California)
• Original Assignee: Regents of the University of California (University of California)
• Inventors: Lal, Ratnesh, Quist, Arjan, Cohen, Daniel, Lin, Hai, Ramachandran, Srinivasan
• Application Number:
  US11/450,888
• Publication Number:
  US 20070117217A1
• Time in Patent Office: Days
• US Class Current: 436/513
• CPC Class Codes: G01N 21/648 using evanescent coupling or surface plasmon coupling for the excitation of fluorescence
• CPC Class Codes: G01N 2800/24 Immunology or allergic disorders
• CPC Class Codes: G01N 33/54373 involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
• CPC Class Codes: G01N 33/6854 Immunoglobulins

Abstract

This invention provides a device and methods for the rapid detection and/or diagnosis and/or characterization of one or more allergies (e.g., causes IgE mediated allergic reaction (immediate hypersensitvity) in a mammal (e.g., a human or a non-human mammal). In certain embodiments, the device comprises a microcantilever array where different cantilevers comprising the array bear different antigens. Binding of IgE to the antigen on a cantilever causes bending of the cantilever which can be readily detected.

Claims

1. A device for detecting and characterizing an allergy, said device comprising:

a sample chamber; and

an array of microcantilevers wherein microcantilevers comprising said array have affixed thereto antigen such that there is a different species of antigen for each allergy it is desired to detect, and different species of antigen are on different microcantilevers in said array, wherein the free ends of the microcantilevers project into the sample chamber.

2. The device of claim 1, wherein said device comprises at least 4 microcantilevers each having affixed thereto different binding moieties.

3. The device of claim 1, wherein said device comprises at least 10 microcantilevers each having affixed thereto different binding moieties.

4. The device of claim 1, wherein said device comprises at least 100 microcantilevers each having affixed thereto different binding moieties.

5. The device of claim 1, wherein said device comprises negative control microcantilevers treated to resist binding by protein.

6. The device of claim 1 or 5, wherein said device comprises positive control microcantilevers having attached thereto an antibody that binds IgE antibodies.

7. The device of claim 6, wherein the antibody that binds to IgE antibodies is a single chain antibody.

8. The device of claim 6, wherein the antibody that binds to IgE antibodies is a monoclonal antibody.

9. The device of claim 1, further comprising a first means of detecting deflection of a cantilever when binding moieties on the cantilever bind a target analyte.

10. The device of claim 9, further comprising a second means of detecting deflection of a cantilever when binding moieties on the cantilever bind a target analyte.

11. The device of claim 9 or 10, wherein said first means and said second means are independently selected from the group consisting of an optical detection means, a piezoresistive detection means, a piezoelectric detection means, and an evanescent wave detection means.

12. The device of claim 1, wherein said allergen is selected from the group consisting of a pet allergen, dust, mold spores, pollen, a food allergen, and an insect bite allergen.

13. A method of identifying an allergy in a subject, said method comprising:

providing a biological sample from said subject comprising IgE antibodies;

contacting said biological sample or a component thereof with a device according to any one of claims 1 through 12; and

detecting deflection of one or more cantilevers in the microcantilever array in response to binding by IgE where binding of the cantilever indicates that said subject has an allergic response to the antigen present on the deflected cantilever.

14. The method of claim 13, wherein said detecting comprises a method selected from the group consisting of detecting an optical signal, detecting a piezoresistive signal, detecting an optical signal, detecting an evanescent wave signal.

15. The method of claim 14, wherein said detecting comprises utilizing at least two different detection methods.

16. The method of claim 13, wherein said sample comprises whole blood, plasma, or serum.

17. A device for detecting the presence, absence, or quanity of a plurality of analytes, said device comprising:

a sample chamber; and

an array of microcantilevers wherein micocantilevers comprising said array have affixed thereto binding moieties such that there is a different species of binding moiety that specifically or preferentially binds each species of analyte that is to be detected; and

different species of binding moiety are on different microcantilevers in said array, wherein the free ends of the microcantilevers project into the sample chamber.

18. The device of claim 17, wherein said device comprises at least 4 microcantilevers each having affixed thereto different binding moieties.

19. The device of claim 17, wherein said device comprises at least 10 microcantilevers each having affixed thereto different binding moieties.

20. The device of claim 17, further comprising a first means of detecting deflection of a cantilever when binding moieties on the cantilever bind a target analyte.

21. The device of claim 20, further comprising a second means of detecting deflection of a cantilever when binding moieties on the cantilever bind a target analyte.

22. The device of claim 20 or 21, wherein said first means and said second means are independently selected from the group consisting of an piezoresistive detection means, a piezoelectric detection means, and an optical detection means.

23. The device of claim 22, wherein said first means and said second means are optical detection means selected from the group consisting of means to detect optical beam deflection, means to detect optical phase shift, means to detect optical intensity shift, and means to detect evanescent field excitation of fluorescence.

24. A device for supporting a sample and for providing evanescent field excitation of fluorescence in total internal reflectance microscopy (TIRFM), said device comprising:

a substantially planar optical waveguide comprising two substantially parallel surfaces; and

an active optical coupler affixed or juxtaposed to said waveguide such that light generated from said coupler enters said waveguide, where said active optical coupler is not a fluorophore.

27. The device of any one of claims 24 or 25, wherein said active optical coupler is an electrically driven coupler or an optically pumped laser.

28. The device of claim 27, wherein said active optical coupler is an electrically driven coupler selected from the group consisting of a light emitting diode (LED), a laser diode, an electroluminescent device, and a microplasma discharge device.

31. The device of any of claims 24 or 26, wherein said device further comprises an angle filter comprising a material whose refractive index is between that of the waveguide and air, where said angle filter is disposed on a surface of said waveguide to substantially reduce light propagating in the waveguide.

32. The device of claim 31, wherein said angle filter substantially eliminates or reduces light propagating in the waveguide at an angle below a critical angle, measured relative to a line perpendicular to the waveguide surface and drawn into the waveguide, said critical angle ranging from about 35 degrees to about 70 degrees.

34. The device of any one of claims 24, 25, or 26, wherein said waveguide has an index of refraction of about 1.4 or more.

35. The device of any one of claims 24, 25, or 26, wherein said waveguide ranges in thickness from about 50 μ

m to about 1 mm.

36. The device of claim 35, wherein said waveguide ranges in thickness from about 50 μ

m to about 500 μ

m.

37. The device of claim 35, wherein said waveguide ranges in thickness from about 100 μ

m to about 200 μ

m.

38. The device of any one of claims 24, 25, or 26, wherein said waveguide comprises a material selected from the group consisting of glass, plastic, and a crystalline material.

39. The device of claim 38, wherein said waveguide comprises a crystalline material selected from the group consisting of quartz, sapphire, silicon carbide, calcium fluoride, aluminum nitride, gallium nitride, aluminum gallium nitride, magnesium fluoride, and lithium niobate.

40. The device of claim 38, wherein said waveguide comprises a coverslip.

41. The device of any one of claims 24, 25, or 26, wherein said device further comprises a substantially planar low refractive index material immediately below the waveguide.

42. The device of claim 41, wherein said low refractive index material has a refractive at least 0.05 below that of the waveguide, and a thickness of at least 1 μ

m.

43. The device of claim 24, 25, or 26, wherein said optical coupler is laminated to said waveguide.

44. The device of any one of claims 24, 25, or 26, wherein said device further comprises a means for supporting or affixing a sample such that all or a portion of said sample is exposed to an evanescent field from said optical waveguide.

45. The device of claim 44, wherein said means comprises one or more fluid reservoirs.

46. The device of any one of claims 24, 25, or 26, wherein said device further comprises a means to measure intensity of an excitation light.

47. The device of claim 46, wherein said means to measure excitation intensity comprises one or more fluorophores that are excited by the same evanescent field used to excite the sample of interest, and that emit fluorescence that is proportional to excitation intensity.

48. The device of claim 47, wherein said fluorophores are distributed on the waveguide surface in known and easily distinguishable patterns.

49. The device of claim 46, wherein said means to measure excitation intensity comprises a photodiode that intercepts a portion of the excitation light.

50. The device of any one of claims 24, 25, or 26, wherein said device further comprises a means to quantify sample distance from the waveguide surface.

51. The device of claim 50, wherein said means to quantify sample distance comprises fluorescent markers at known distances from the waveguide surface.

52. The device of claim 50, wherein said means to quantify sample distance comprises two or more couplers emitting light at significantly different wavelengths, in conjunction with a sample fluorophore that can be excited by light at significantly different wavelengths.

53. The device of any one of claims 24, 25, or 26, wherein said device further comprises structures that reduce scattering of excitation light at boundaries of fluids disposed on the waveguide surface, or at boundaries of structures that contain those fluids.

54. The device of claim 53, wherein said structures comprise an antireflection layer and/or an absorption layer.

55. The device of claim 53, wherein said structures are selected from the group consisting of structures fabricated from material with an index of refraction approximately equal to that of the contained fluid, and structures with reentrant profiles such that light scattered at the point of contact between the structure and the substrate is subsequently intercepted and absorbed by another part of the structure.

56. The device of any one of claims 24, 25, or 26, wherein the planar surface opposite the sample is coated with a smooth and transparent layer of thickness greater than approximately one micrometer and index of refraction lower than that of the waveguide, such that light trapped by total internal reflection in the waveguide does not penetrate evanescently to the surface of said layer.

57. The device of any one of claims 24, 25, or 26, wherein a solid or liquid layer is disposed on the substrate such that excitation light propagating within the waveguide within some range of propagation angles relative to the planar surface is transmitted out of the substrate and into the solid or liquid layer, and is subsequently transmitted away from the device or absorbed.

58. The device of any one of claims 24, 25, or 26, wherein a planar surface opposite the sample is coated with an absorptive or reflective optical filter, such that only sample fluorescence of selected wavelengths is transmitted through the filter.

59. The device of any one of claims 24, 25, or 26, wherein said device is disposable.

25. A device for supporting a sample and for providing evanescent field excitation of fluorescence in total internal reflectance microscopy (TIRFM), said device comprising:

a substantially planar optical waveguide comprising two substantially parallel surfaces;

an active optical coupler affixed or juxtaposed to said waveguide such that light generated from said coupler enters said waveguide; and

an angle filter comprising a material whose refractive index is between that of the waveguide and air, where said angle filter is disposed on a surface of said waveguide to substantially reduce light propagating in the waveguide within a predetermined range of angles.

29. The device of claim 25, wherein said active optical coupler is a fluorophore.

33. The device of claim 25, wherein said angle filter substantially eliminates or reduces light propagating in the waveguide at an angle below a critical angle, measured relative to a line perpendicular to the waveguide surface and drawn into the waveguide, said critical angle ranging from about 35 degrees to about 70 degrees.

26. A device for supporting a sample and for providing evanescent field excitation of fluorescence in total internal reflectance microscopy (TIRFM), said device comprising:

a substantially planar optical waveguide comprising two substantially parallel surfaces; and

a passive optical coupler affixed or juxtaposed to said waveguide such that light provided from said coupler enters said waveguide.

30. The device of claim 26, wherein said passive optical coupler is selected from the group consisting of a lens, a prism, a facet, a grating, a mirror, a gradient index structure, and a scattering structure.