Substrates, systems and methods for analyzing materials
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
G01N-021/64
C12Q-001/68
G01N-021/77
G02B-006/43
출원번호
US-0084422
(2013-11-19)
등록번호
US-9029802
(2015-05-12)
발명자
/ 주소
Lundquist, Paul
Turner, Stephen
출원인 / 주소
Pacific Biosciences of California, Inc.
대리인 / 주소
Arnold, Deana A.
인용정보
피인용 횟수 :
10인용 특허 :
80
초록▼
Substrates, systems and methods for analyzing materials that include waveguide arrays disposed upon or within the substrate such that evanescent fields emanating from the waveguides illuminate materials disposed upon or proximal to the surface of the substrate, permitting analysis of such materials.
Substrates, systems and methods for analyzing materials that include waveguide arrays disposed upon or within the substrate such that evanescent fields emanating from the waveguides illuminate materials disposed upon or proximal to the surface of the substrate, permitting analysis of such materials. The substrates, systems and methods are used in a variety of analytical operations, including, inter alia, nucleic acid analysis, including hybridization and sequencing analyses, cellular analyses and other molecular analyses.
대표청구항▼
1. An analytical device, comprising: a substrate comprising a first surface and at least a first optical waveguide disposed upon the first surface;an optically resolvable molecular complex immobilized within a confined region and sufficiently proximal to the first surface to be illuminated by an eva
1. An analytical device, comprising: a substrate comprising a first surface and at least a first optical waveguide disposed upon the first surface;an optically resolvable molecular complex immobilized within a confined region and sufficiently proximal to the first surface to be illuminated by an evanescent field emanating from the optical waveguide when light is passed through said optical waveguide; andat least a first excitation radiation source optically coupled to the substrate to provide the evanescent field by passing excitation light into the optical waveguide. 2. The device of claim 1, wherein a core of the optical waveguide is exposed at the first surface of the substrate in the confined region. 3. The device of claim 1, further comprising at least one filter integrated into the substrate. 4. The device of claim 1, further comprising at least one grating integrated into the substrate. 5. The device of claim 1, further comprising a mask layer disposed over the first surface of the substrate, wherein the mask layer comprises an aperture disposed therethrough, the aperture providing the confined region within which the optically-resolvable molecular complexes is immobilized. 6. The device of claim 5, wherein portions of the mask layer lacking the apertures block the evanescent field emanating from the array. 7. The device of claim 5, wherein the apertures are optical confinements. 8. The device of claim 1, wherein the optically resolvable molecular complex comprises an enzyme. 9. The device of claim 8, wherein the enzyme is a polymerase. 10. The device of claim 1, wherein the optically resolvable molecular complex comprises an individual analyte comprising a fluorescent or fluorogenic label that emits a signal in response to the excitation light. 11. A method of detecting a signal from an analyte, comprising: providing a substrate comprising a) a first surface;b) at least a first optical waveguide proximal to the first surface;c) a plurality of optically resolvable molecular complexes immobilized within confined regions and sufficiently proximal to the first optical waveguide to be illuminated by an evanescent field emanating from the first optical waveguide when light is passed through said optical waveguide;exposing the first surface to an analyte comprising a fluorescent or fluorogenic moiety that emits a signal in response to the evanescent field;directing light through the first optical waveguide such that the evanescent field from the waveguide illuminates the optically resolvable molecular complexes; andupon interaction of the analyte with one of the optically resolvable molecular complexes, detecting a signal from the analyte. 12. The method of claim 11, wherein the confined regions are within apertures in a mask layer disposed over the first surface. 13. The method of claim 12, wherein the mask layer blocks the evanescent field above portions of the substrate that are not disposed beneath one of the apertures. 14. The method of claim 12, wherein the apertures are optical confinements. 15. The method of claim 11, wherein each of the optically resolvable molecular complexes comprises a polymerase enzyme in a complex with a target nucleic acid and a primer complementary to a portion of the target nucleic acid; and wherein the analyte is a nucleotide or nucleotide analog. 16. The method of claim 11, wherein the substrate further comprises at least one grating integrated into the substrate. 17. The method of claim 11, wherein the substrate further comprises at least one filter integrated into the substrate. 18. The method of claim 11, wherein the first optical waveguide is exposed at the first surface of the substrate within the confined regions. 19. The method of claim 11, wherein the fluorescent or fluorogenic moiety is removed from the analyte during the interaction. 20. A method of determining a nucleotide sequence of a template nucleic acid, the method comprising: providing a substrate comprising a first surface and at least a first optical waveguide proximal to the first surface of the substrate;immobilizing an optically resolvable polymerase enzyme in a confined region sufficiently proximal to the first optical waveguide to be illuminated by an evanescent field emanating from the first optical waveguide, wherein the polymerase enzyme is further bound to the template nucleic acid, which is further bound to a primer;directing light through the first optical waveguide such that the evanescent field from the waveguide illuminates the confined region;incorporating a plurality of nucleotides into a nascent strand complementary to the template nucleic acid using template-directed synthesis catalyzed by the polymerase enzyme, wherein for each of the nucleotides incorporated into the nascent strand, an identity of a base comprised therein is determined by detecting a signal produced by said each of the nucleotides when exposed to the evanescent field, thereby determining a nucleotide sequence of the nascent strand; anddetermining a complementary nucleotide sequence that is complementary to the nucleotide sequence of the nascent strand, wherein the complementary nucleotide sequence is the nucleotide sequence of the template nucleic acid. 21. The method of claim 20, wherein a plurality of optically resolvable polymerase enzymes are immobilized in a plurality of confined regions. 22. The method of claim 20, wherein the incorporating is done in real time without the use of terminator chemistries. 23. The method of claim 20, wherein the substrate further comprises at least one grating integrated into the substrate. 24. The method of claim 20, wherein the substrate further comprises at least one filter integrated into the substrate. 25. The method of claim 20, wherein the first optical waveguide is exposed at the first surface of the substrate within the confined region.
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