Plasmon resonance biosensor and method

• US 7,745,143 B2
• Filed: 11/18/2005
• Issued: 06/29/2010
• Est. Priority Date: 11/19/2004
• Status: Active Grant

• Current Assignee: Suzhou Puxin Life Science & Technology Limited
• Original Assignee: Plexera, LLC
• Inventors: Casasanta, Vincenzo III
• Primary Examiner(s): CHEU, CHANGHWA J
• Application Number:
  US11/282,272
• Publication Number:
  US 20060134669A1
• Time in Patent Office: 1,684 Days
• Field of Search: 435/7.1, 435/7.2, 435/7.91, 435/7.92
• US Class Current: 435/7.1
• CPC Class Codes: G01N 21/553 and using surface plasmons fluorescence excitation G01N21/648; enhanced Raman G01N21/658
• CPC Class Codes: G01N 33/54373 involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings

Abstract

A method of analyzing a sample comprising directing a beam of light to a spot on the surface of a microarray treated with the sample using a digital micromirror device, and observing the SPR spectral shift due to a chemical binding event. The digital micromirror device can be, for example, that used in Digital Light Processing (DLP). Such a device can selectively place a pixel of light onto a microarray such that each spot can be observed at millisecond intervals and the whole microarray can be sequentially scanned over a relatively short period. The SPR spectral shift for each spot can be measured as a function of time, thus producing SPR detection of molecular binding in an array format.

Claims

1. A method for analyzing a sample comprising:

(a) providing a microarray comprising a surface having a plurality of discrete locations, each of which includes a first member of a chemical binding pair and is associated with a surface plasmon resonance;

(b) irradiating the discrete locations on the surface of the microarray with a light beam using an apparatus comprising a light source, a digital micromirror device, and a prism or lens located between the digital micromirror device and the surface of the microarray;

(c) contacting the surface of the microarray with a sample comprising a second member of the chemical binding pair, whereupon, in at least one of the discrete locations, the second member of the chemical binding pair binds to the first member of the chemical binding pair on the surface of the microarray and causes a spectral shift in the surface plasmon resonance associated with the discrete location where the chemical binding occurs; and

(d) detecting the surface plasmon resonance spectral shift associated with each location as a function of time therefore providing surface plasmon resonance detection of chemical binding with said sample in an array format.

2. The method according to claim 1 wherein the surface has at least 100 discrete locations.

3. The method according to claim 1 wherein the surface has at least 1000 discrete locations.

4. The method according to claim 1 wherein each discrete location comprises a thin metal pad on which the first member of the chemical binding pair is immobilized.

5. The method according to claim 1 wherein the apparatus comprises a hemispherical prism.

6. The method according to claim 1 wherein the light source comprises a polychromatic broadband light source that emits light having wavelengths in the range of 200 nm to 2000 nm.

7. The method according to claim 1 wherein the first member of the specific binder pair comprises a first functional group that reacts with the surface of the microarray at the discrete location to immobilize the first member on the surface of the microarray at the discrete location.

8. The method according to claim 7 wherein the first functional group is selected from the group consisting of an amine, a carboxylic acid or derivative thereof, a thiol, a maleimide, a biotin, a hapten, an antigen, an antibody, an oligonucleotide, and combinations thereof.

9. The method according to claim 7 wherein the first functional group immobilizes the first member of the chemical binding pair on the surface of the microarray through a second functional group that forms a covalent bond with the surface of the microarray at the discrete location.

10. The method according to claim 9 wherein the first functional group is biotin, the second functional group is a thiol, and the surface of the microarray at the discrete location comprises gold.

11. The method according to claim 1 wherein the surface of the microarray at the discrete location comprises a third functional group that reacts with the first member of the specific binder pair to immobilize the first member on the surface of the microarray at the discrete location.

12. The method according to claim 11 wherein the third functional group is selected from the group consisting of an amine, a carboxylic acid or derivative thereof, a thiol, a maleimide, a biotin, a hapten, an antigen, an antibody, an oligonucleotide, and combinations thereof.

13. The method according to claim 11 wherein the third functional group immobilizes the first member of the chemical binding pair on the surface of the microarray through a fourth functional group that forms a covalent bond with the first member of the chemical binding pair.

14. The method according to claim 13 wherein the third functional group is biotin, the second functional group is a thiol, and the surface of the microarray at the discrete location comprises gold.

15. The method according to claim 1 wherein the chemical binding pair comprises a biotin/avidin pair.

16. The method according to claim 1 wherein the chemical binding pair comprises a hapten/antibody pair.

17. The method according to claim 1 wherein the chemical binding pair comprises an antigen/antibody pair.

18. The method according to claim 1 wherein the chemical binding pair comprises a peptide/peptide pair.

19. The method according to claim 1 wherein the chemical binding pair comprises complementary strands of DNA.

20. The method according to claim 1 wherein the chemical binding pair comprises complementary strands of RNA.

21. The method of claim 1, wherein the digital micromirror device periodically addresses a sequence of the discrete locations.

22. The method of claim 21, wherein detecting a spectrum shift is performed by collecting non-imaged light from the discrete locations with a spectrometer.

23. The method of claim 1, wherein the microarray surface is a two-dimensional surface and the plurality discrete locations are disposed across the microarray surface in a two-dimensional array.