Scanning analyzer for single molecule detection and methods of use
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
G01N-021/00
B01L-003/00
G01N-015/14
G01N-021/64
G01N-033/53
G01N-021/01
G01N-015/00
출원번호
US-0579442
(2014-12-22)
등록번호
US-9239284
(2016-01-19)
발명자
/ 주소
Livingston, Richard
출원인 / 주소
Singulex, Inc.
대리인 / 주소
McDonnell Boehnen Hulbert & Berghoff LLP
인용정보
피인용 횟수 :
1인용 특허 :
128
초록▼
The invention encompasses analyzers and analyzer systems that include a single molecule analyzer, methods of using the analyzer and analyzer systems to analyze samples, either for single molecules or for molecular complexes. The single molecule uses electromagnetic radiation that is translated throu
The invention encompasses analyzers and analyzer systems that include a single molecule analyzer, methods of using the analyzer and analyzer systems to analyze samples, either for single molecules or for molecular complexes. The single molecule uses electromagnetic radiation that is translated through the sample to detect the presence or absence of a single molecule. The single molecule analyzer provided herein is useful for diagnostics because the analyzer detects single molecules with zero carryover between samples.
대표청구항▼
1. A analyzer for determining an analyte, comprising: (a) an electromagnetic radiation source for providing electromagnetic radiation;(b) a system for directing the electromagnetic radiation from the electromagnetic radiation source to an interrogation space in a sample container;(c) a translating s
1. A analyzer for determining an analyte, comprising: (a) an electromagnetic radiation source for providing electromagnetic radiation;(b) a system for directing the electromagnetic radiation from the electromagnetic radiation source to an interrogation space in a sample container;(c) a translating system for translating the interrogation space through at least a portion of the sample container, thereby forming a moveable interrogation space;(d) a detector for detecting electromagnetic radiation emitted from a photon emitting species in the interrogation space if the species is present, wherein the detector is operably connected to the interrogation space, and(e) a processor operatively connected to the detector, wherein the processor determines a threshold photon value corresponding to a background signal in the interrogation space, determines the presence of a photon emitting species comprising or corresponding to the analyte in the interrogation space in each of the plurality of bins by identifying bins having a photon value greater than the threshold value, and relates the number of bins having a photon value greater than the threshold level to the presence or amount of the analyte in the sample. 2. The analyzer of claim 1, wherein the translating system can translate the interrogation space in one or more of a linear path and a non-linear path. 3. The analyzer of claim 2, wherein the non-linear path comprises a substantially circular path, a helical path, or a raster pattern. 4. The analyzer of claim 1, wherein an electromagnetic radiation beam from the electromagnetic radiation source can be moved relative to a fixed sample container. 5. The analyzer of claim 1, wherein the sample container can be moved relative to a fixed electromagnetic radiation beam from the electromagnetic radiation source. 6. The analyzer of claim 1, wherein the sample container and an electromagnetic radiation beam from the electromagnetic radiation source can be moved relative to each other. 7. The analyzer of claim 1, wherein the translating system comprise a tilted mirror mounted on the end of a scan motor shaft, wherein the mirror deflects an electromagnetic radiation beam from the electromagnetic radiation source to the sample container. 8. The analyzer of claim 1, wherein the translating system comprises an optical wedge mounted to a shaft of the electromagnetic radiation source. 9. The analyzer of claim 1, wherein the interrogation space is of a volume between about 15 μm3 and about 11000 μm3. 10. The analyzer of claim 1, wherein the threshold photon value is a function of the background photon level. 11. The analyzer of claim 10, wherein the threshold photon value is a fixed number of standard deviations above the background photon level. 12. The analyzer of claim 1, wherein the processer determines detection events representing photon bin counts above a threshold photon value as a photon emitting species comprising or corresponding to a single molecule of the analyte so that each bin is analyzed as a “yes” or “no” for the presence of the photon emitting species. 13. The system of claim 1, wherein the electromagnetic radiation source is a laser having a power output of 1-20 mW. 14. The analyzer of claim 1, wherein the photon emitting species comprises a label that emits photons when stimulated by electromagnetic energy, the label comprising a binding partner specific for the analyte. 15. The analyzer of claim 14, wherein the label further comprises a fluorescent moiety. 16. The analyzer of claim 1, wherein bins have a duration of 10-2000 microseconds. 17. The analyzer of claim 1, wherein the electromagnetic radiation source is a continuous wave electromagnetic radiation source. 18. The analyzer of claim 17, wherein the continuous wave electromagnetic radiation source is a light-emitting diode or a continuous wave laser. 19. The analyzer of claim 1, further comprising a microscope objective wherein a depth of field of the microscope objective and a diameter of an aperture imaged to the microscope objective together define the interrogation space. 20. The analyzer of claim 1, further comprising a microscope objective wherein a depth of field of the microscope objective and a lateral extent of an electromagnetic radiation beam together define the interrogation space. 21. The analyzer of claim 1, further comprising an attenuator operatively connected between the interrogation space and the detector and configured to receive electromagnetic radiation emitted from the interrogation space, wherein the processor is further configured to output instructions to the attenuator to attenuate the electromagnetic radiation from the interrogation space when number of photons detected in one or more bins exceeds a saturation threshold. 22. The analyzer of claim 1, wherein the processor is further configured to determine the presence or amount of the photon emitting species by measuring a total number of photons per bin. 23. The analyzer of claim 1, further comprising a confocal optical arrangement for deflecting a laser beam onto said interrogation space and for imaging a stimulated photon emitting species, wherein said confocal optical arrangement comprises an objective lens having a numerical aperture of at least 0.8. 24. The analyzer in claim 1, wherein the total energy received by the interrogation space from the electromagnetic radiation source during each bin is 0.1 to 10 micoJoules. 25. The analyzer of claim 1, wherein the electromagnetic radiation source stimulates the moiety for a duration of less than 1000 microseconds. 26. The analyzer of claim 1, wherein the bin time is longer than the time the moiety passes through the interrogation space. 27. The analyzer of claim 1, wherein the bin time is one-half to two times longer than the time the moiety passes through the interrogation space. 28. The analyzer of claim 1, wherein the bin time is the same as the time that the moiety passes through the interrogation space. 29. The analyzer of claim 1, wherein the translating system is constructed and arranged to translate through a same portion of sample a first time and a second time to allow a photon emitting species, if present, detected the first time the interrogation space is translated through the portion of sample to substantially diffuse out of the portion of sample after the first time the portion of sample is interrogated by the interrogation space and to further allow a subsequent light emitting species, if present, to substantially diffuse into the portion of sample the second time the portion of sample is interrogated by the interrogation space. 30. The analyzer of claim 29, wherein the translating system is constructed and arranged to translate the interrogation space in a substantially circular pattern, wherein the system is capable of translating the interrogation space at a speed of between 100 and 1000 RPM. 31. The analyzer of claim 1, wherein the translating system is constructed and arranged to translate the interrogation space such that the detection spot returns to the portion of sample after sufficient time has passed so that the species detected in the first pass can diffuse out of the portion, and other species can diffuse into the portion. 32. An analyzer system comprising the analyzer of claim 1 and a fluorescent moiety that is capable of emitting at least 200 photons when simulated by a laser emitting light at the excitation wavelength of the moiety, wherein the laser is focused on a spot not less than 5 microns in diameter that contains the moiety, and wherein the total energy directed at the spot by the laser is no more than 3 microJoules. 33. The system of claim 32, wherein the fluorescent moiety is low photobleaching. 34. A method for detecting the presence or amount of an analyte in a sample comprising: (a) directing electromagnetic radiation from an electromagnetic radiation source to an interrogation space in the sample;(b) detecting the presence or absence of a photon emitting species comprising or corresponding to the analyte in the interrogation space located at a first position in the sample;(c) translating the interrogation space through the sample to a subsequent position in the sample;(d) detecting the presence or absence of a subsequent photon emitting species comprising or corresponding to the analyte in the subsequent position in the sample; and(e) repeating steps (c) and (d) as required to detect the presence or absence of the photon emitting species in more than one position of the sample, wherein the presence or amount of an analyte in a sample is determined by determining a threshold photon value corresponding to a background signal in the interrogation space, and determining the presence of the photon emitting species comprising or corresponding to the analyte in the interrogation space in each of the plurality of bins by identifying bins having a photon value greater than the threshold value. 35. The method of claim 34, wherein the threshold photon value is a function of the background photon level. 36. The method of claim 35, wherein the threshold photon value is a fixed number of standard deviations above the background photon level. 37. The method of claim 34, wherein the processer determines detection events representing photon bin counts above a threshold photon value as the photon emitting species corresponding to a single molecule of the analyte so that each bin is analyzed as a “yes” or “no” for the presence of the photon emitting species. 38. The method of claim 34, wherein the interrogation space is of a volume between about 15 μm3 and about 11000 μm3. 39. The method of claim 34, wherein the interrogation space is translated in a non-linear path. 40. The method of claim 34, wherein the interrogation space is translated through the first position of sample as to allow a photon emitting species, if present, detected the first time the interrogation space is translated through the position of sample to substantially diffuse out of the position of sample after the first time the position of sample is interrogated by the interrogation space and to further allow a subsequent photon emitting species, if present, to substantially diffuse into the position of sample the second time the position of sample is interrogated by the interrogation space. 41. The method of claim 34, wherein the interrogation space is translated such that the detection spot returns to the first position of sample after sufficient time has passed so that a photon emitting species detected in the first pass can diffuse out of the position, and another photon emitting species can diffuse into the position.
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Baer Thomas M. (Mountain View CA) Dietz Louis J. (Mountain View CA) Dubrow Robert S. (San Carlos CA) Hayter Paul G. (Los Altos CA) Hodges Michael (Palo Alto CA) Manian Bala S. (Los Altos Hills CA) Sh, Apparatus and method for volumetric capillary cytometry.
Groman Ernest V. (Brookline MA) Josephson Lee (Arlington MA), Biologically degradable superparamagnetic particles for use as nuclear magnetic resonance imaging agents.
Mathies Richard A. (Contra Costa County CA) Huang Xiaohua C. (Santa Clara County CA) Quesada Mark A. (San Francisco County CA), Capillary array confocal fluorescence scanner and method.
Chow Calvin Y. H. ; Parce John Wallace ; McReynolds Richard J. ; Kennedy Colin B. ; Bousse Luc J., Controller/detector interfaces for microfluidic systems.
Hoffman Michael A. (Carmel CA), Fluorescent-particle analyzer with timing alignment for analog pulse subtraction of fluorescent pulses arising from diff.
Wada, H. Garrett; Kopf-Sill, Anne R.; Alajoki, Marja Liisa; Parce, J. Wallace; Wang, Benjamin N.; Chow, Andrea W.; Dubrow, Robert S., Focusing of microparticles in microfluidic systems.
Swedberg Sally A. (Los Altos CA) Kaltenbach Patrick (Bischweier DEX) Witt Klaus E. (Keltern DEX) Bek Fritz (Waldbronn DEX) Mittelstadt Laurie S. (Belmont CA), Fully integrated miniaturized planar liquid sample handling and analysis device.
Dollinger Gavin D. (San Francisco CA) Cunico Robert L. (Hercules CA) Kunitani Michael G. (San Rafael CA), HPLC light scattering detector for biopolymers.
Mathies Richard A. (Contra Costa County CA) Peck Konan (Contra Costa County CA) Stryer Lubert (Santa Clara County CA), High sensitivity fluorescent single particle and single molecule detection apparatus and method.
Ambrose W. Patrick ; Grace W. Kevin ; Goodwin Peter M. ; Jett James H. ; Orden Alan Van ; Keller Richard A., High throughput analysis of samples in flowing liquid.
Gourley Paul L. (12508 Loyola ; NE. Albuquerque NM 87112) Gourley Mark F. (7509 Spring Lake Dr. ; Apt. B1 Bethesda MD 20817), Laser apparatus and method for microscopic and spectroscopic analysis and processing of biological cells.
Witt Klaus E. (Keltern DEX) Kaltenbach Patrick (Bischweier DEX) Bek Fritz (Waldbronn DEX) Swedberg Sally A. (Los Altos CA) Mittelstadt Laurie S. (Belmont CA), Low voltage miniaturized column analytical apparatus and method.
Miltenyi Stefan (Moitzfeld 60a ; D-5060 Bergisch Gladbach 1 Cologne DEX) Radbruch Andreas (Bonn DEX) Weichel Walter (Cologne DEX) Muller Werner (Cologne DEX) Gottlinger Christoph (Cologne DEX) Meyer , Metal matrices for use in high gradient magnetic separation of biological materials and method for coating the same.
Begg Geoffrey Stephen (Heidelberg AUX) Simpson Richard John (Richmond AUX) Burgess Antony Wilks (Camberwell AUX), Method allowing sequential chemical reactions.
Purvis ; Jr. Norman B. (1010 Lawnview Ct. Franklin TN 37064) Giorgio Todd D. (3608 Westbrook Dr. Nashville TN 37205), Method and apparatus for determining absolute particle size, surface area and volume normalized fluorescence using forwa.
Cherukuri Satyam C. (Cranbury NJ) Demers Robert R. (Cranbury NJ) Fan Zhong H. (Middlesex NJ) Levine Aaron W. (Lawrenceville NJ) McBride Sterling E. (Lawrence Township ; Mercer County NJ) Zanzucchi Pe, Method and system for inhibiting cross-contamination in fluids of combinatorial chemistry device.
Eigen Manfred,DEX ; Winkler Thorsten,DEX ; Stephan Jens,DEX ; Schwille Petra,DEX ; Koltermann Andre,DEX ; Kettling Ulrich,DEX ; Dorre Klaus,DEX ; Bieschke Jan,DEX, Method for detecting reactions by means of coincidence analysis.
Seidel Claus,DEX ; Gunther Rolf,DEX ; Lupke Stefan,DEX, Method for differentiating or detecting particles in a sample by identifying signal segments of time-resolved, optical raw signals from the sample on the basis of single photon detection.
Goix, Philippe J.; Puskas, Robert; Todd, John; Livingston, Richard A.; Held, Douglas, Method for highly sensitive detection of single protein molecules labeled with fluorescent moieties.
Robotti, Karla M.; Yin, Hongfeng, Methods and using chemico-mechanical microvalve devices for the selective separation of components from multi-component fluid samples.
Fauver, Mark E.; Seibel, Eric J.; Brown, Chris M.; Reinhall, Per G.; Smithwick, Quinn Y. J., Micro-fabricated optical waveguide for use in scanning fiber displays and scanned fiber image acquisition.
Richard A. Mathies ; Pankaj Singhal ; Jin Xie ; Alexander N. Glazer, Microfabricated capillary electrophoresis chip and method for simultaneously detecting multiple redox labels.
Kaltenbach Patrick,DEX ; Swedberg Sally A. ; Witt Klaus E.,DEX ; Bek Fritz,DEX ; Mittelstadt Laurie S., Miniaturized planar columns for use in a liquid phase separation apparatus.
Kaltenbach Patrick (Bischweier DEX) Swedberg Sally A. (Los Altos CA) Witt Klaus E. (Keltern DEX) Bek Fritz (Waldbronn DEX) Mittelstadt Laurie S. (Belmont CA), Miniaturized planar columns in novel support media for liquid phase analysis.
Hollis Mark A. (Concord MA) Ehrlich Daniel J. (Lexington MA) Murphy R. Allen (Boxboro MA) Kosicki Bernard B. (Acton MA) Rathman Dennis D. (Ashland MA) Chen Chang-Lee (Sudbury MA) Mathews Richard H. (, Optical and electrical methods and apparatus for molecule detection.
Goodwin Peter M. ; Jett James H. ; Keller Richard A. ; Van Orden Alan K. ; Machara Nicholas P., Single molecule identification using selected fluorescence characteristics.
Galambos, Paul C.; Okandan, Murat; Montague, Stephen; Smith, James H.; Paul, Phillip H.; Krygowski, Thomas W.; Allen, James J.; Nichols, Christopher A.; Jakubczak, II, Jerome F., Surface-micromachined microfluidic devices.
Doth Margit,DEX ; Petry Christoph,DEX, Synthetic calibrators for use in immunoassays, comprising the analytes or partial sequences thereof which are conjugated to inert carrier molecules.
Myers Stephen A. (25 Nimitz Pl. Old Greenwich CT 06870), System and method for determining changes in fluorescence of stained nucleic acid in electrophoretically separated bands.
Muller Ralph,DEX ; Sauer Markus,DEX ; Zander Christoph,DEX, System for distinguishing fluorescent molecule groups by time resolved fluorescence measurement.
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