# US 7,745,143 B2 · Plasmon resonance biosensor and method > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 7,745,143 B2 - Document ID: US7745143B2 - Status: Granted - Kind: B2 - Application number: 11/282,272 - Filed: 2005-11-18 - Published: 2006-06-22 - Granted: 2010-06-29 - Earliest claimed: 2004-11-19 - Assignees: Plexera LLC - Inventors: Vincenzo Casasanta, III - Web page: https://patentgrep.com/patent/US7745143B2 ## CPC - G01N 21/553: {and using surface plasmons (fluorescence excitation G01N21/648; enhanced Raman G01N21/658)} - G01N 33/54373: {involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings} - G01N: INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES (measuring or testing apparatus or processes other than immunoassay, involving enzymes or microorganisms C12M, C12Q) ## 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 ### Claim 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. ### Claim 2 (depends on 1) The method according to claim 1 wherein the surface has at least 100 discrete locations. ### Claim 3 (depends on 1) The method according to claim 1 wherein the surface has at least 1000 discrete locations. ### Claim 4 (depends on 1) 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. ### Claim 5 (depends on 1) The method according to claim 1 wherein the apparatus comprises a hemispherical prism. ### Claim 6 (depends on 1) 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. ### Claim 7 (depends on 1) 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. ### Claim 8 (depends on 7) 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. ### Claim 9 (depends on 7) 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. ### Claim 10 (depends on 9) 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. ### Claim 11 (depends on 1) 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. ### Claim 12 (depends on 11) 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. ### Claim 13 (depends on 11) 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. ### Claim 14 (depends on 13) 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. ### Claim 15 (depends on 1) The method according to claim 1 wherein the chemical binding pair comprises a biotin/avidin pair. ### Claim 16 (depends on 1) The method according to claim 1 wherein the chemical binding pair comprises a hapten/antibody pair. ### Claim 17 (depends on 1) The method according to claim 1 wherein the chemical binding pair comprises an antigen/antibody pair. ### Claim 18 (depends on 1) The method according to claim 1 wherein the chemical binding pair comprises a peptide/peptide pair. ### Claim 19 (depends on 1) The method according to claim 1 wherein the chemical binding pair comprises complementary strands of DNA. ### Claim 20 (depends on 1) The method according to claim 1 wherein the chemical binding pair comprises complementary strands of RNA. ### Claim 21 (depends on 1) The method of claim 1, wherein the digital micromirror device periodically addresses a sequence of the discrete locations. ### Claim 22 (depends on 21) The method of claim 21, wherein detecting a spectrum shift is performed by collecting non-imaged light from the discrete locations with a spectrometer. ### Claim 23 (depends on 1) 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.