IP Library › Granted Patent US 10,724,090
Granted Patent B2
US 10,724,090 · App. 16/385,840 · Granted Jul 28, 2020

Integrated analytical system and method

Inventors: Nathaniel Joseph McCaffrey (Mill Valley, CA); Stephen Turner (Eugene, OR); Ravi Saxena (Millbrae, CA); Scott Edward Helgesen (Palo Alto, CA)
Assignee: Pacific Biosciences of California, Inc.
C12Q1/6874B01L3/502707B01L3/502715B82Y20/00C12Q1/6825C12Q1/6869G01N21/03G01N21/0303G01N21/05G01N21/64G01N21/645G01N21/648G01N21/6428G01N21/6452G01N21/6454G01N21/6456G01N21/75G01N21/77G01N33/54373G02B6/1226B01L2300/0654B01L2300/0663B01L2300/0816B01L2300/168G01N2021/0346G01N2021/6434G01N2021/6439G01N2021/6441G01N2021/6463G01N2021/757G01N2021/7786G01N2201/067G01N2201/068G01N2201/08Y10T436/143333
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Quick Facts
Patent No.
US 10,724,090
App. No.
16/385,840
Granted
Jul 28, 2020
Kind
B2
Abstract

An analytical assembly within a unified device structure for integration into an analytical system. The analytical assembly is scalable and includes a plurality of analytical devices, each of which includes a reaction cell, an optical sensor, and at least one optical element positioned in optical communication with both the reaction cell and the sensor and which delivers optical signals from the cell to the sensor. Additional elements are optionally integrated into the analytical assembly. Methods for forming and operating the analytical system are also disclosed.

Claims (43)

1. A method for distinguishing fluorescently labeled species at a single molecule level comprising:

providing pulsed illumination to an integrated chip, wherein the pulsed illumination comprises two or more pulses at different wavelengths and different times;

the integrated chip comprising:

a plurality of analytical devices, each analytical device having a reaction cell, an optical element, and a detection element; wherein the optical element is in optical communication with the reaction cell and the detection element;

one or more integrated waveguides in optical communication with the reaction cells to deliver the pulsed illumination to the reaction cells;

a fluidic region in fluidic contact with the reaction cells, the fluidic region comprising a sample comprising multiple types of fluorescently labeled species;

whereby for each analytical device in the plurality of analytical devices, the pulsed illumination produces excitation events from the multiple types of fluorescently labeled species within the reaction cell, wherein an excitation event produces an emitted signal detected at the detection element;

distinguishing between the multiple types of fluorescently labeled species within the sample by correlating the timing of the emitted signal detected at the detection element with the timing of the excitation event.

2. The method of claim 1 , wherein the pulsed illumination is provided by multiple excitation sources.

3. The method of claim 2 , wherein the excitation sources comprise one or more lasers.

4. The method of claim 1 , wherein the pulsed illumination includes modulating or interleaving two or more different wavelength excitation sources.

5. The method of claim 1 , wherein each detection element comprises a plurality of storage elements.

6. The method of claim 5 , wherein each detection element comprises four storage elements.

7. The method of claim 5 , wherein each of the storage elements is gated by the activation of a separate excitation source.

8. The method of claim 1 , wherein the sequencing chip comprises at least 1000 analytical devices, at least 10,000 analytical devices, at least 100,000 analytical devices, or at least 1,000,000 analytical devices.

9. The method of claim 1 , wherein the fluorescently labeled species comprise fluorescently labeled nucleic acids.

10. The method of claim 9 , wherein the method comprises nucleic acid sequencing.

11. The method of claim 9 , wherein there are four fluorescently labeled nucleic acids.

12. A method for distinguishing fluorescently labeled species at a single molecule level comprising:

providing pulsed illumination to an integrated chip;

the integrated chip comprising:

a plurality of analytical devices, each analytical device having a reaction cell, an optical element, and a detection element; wherein the optical element is in optical communication with the reaction cell and the detection element;

one or more integrated waveguides in optical communication with the reaction cells to deliver the pulsed illumination to the reaction cells;

a fluidic region in fluidic contact with the reaction cells, the fluidic region comprising a sample comprising multiple types of fluorescently labeled species;

whereby for each analytical device in the plurality of analytical devices, the pulsed illumination produces excitation events from the multiple types of fluorescently labeled species within the reaction cell, wherein an excitation event produces a signal at the detection element; and

distinguishing between the multiple types of fluorescently labeled species within the sample by correlating the timing of the signal at the detection element with the timing of the excitation event;

wherein each detection element comprises a plurality of storage elements;

wherein the excitation events produce emitted photons, wherein the detection element: converts the photons into charges; relegates each respective charge into a storage element in the plurality of storage elements; and integrates the charges over time in each storage element in the plurality of storage elements to generate a plurality of electrical data signals.

13. The method of claim 12 , wherein the plurality of electrical data signals are transmitted off of the chip.

14. The method of claim 12 , wherein the relegation of each respective charge into a storage element is based on the timing of a corresponding excitation source of the pulsed illumination light, a delay between the corresponding excitation and subsequent emission, an arrival time of the photon at the detection element relative to the corresponding excitation source of the pulsed illumination light, or any combination thereof.

15. The method of claim 12 , wherein the multiple types of fluorescently labeled species each have different excitation spectra; the pulsed illumination comprises a plurality of excitation sources at different wavelengths; and the detection element is configured as a vertical detector, and the relegation of each respective charge into a storage element is based on a depth of absorption of the photon that relates to an energy level of the photon.

16. The method of claim 12 , wherein the relegation of each respective charge into a storage element is based on an arrival time of the photon at the detection element relative to a corresponding pulse of the pulsed illumination light.

17. The method of claim 12 , wherein the electrical data signals are representative of a decay of a type of fluorescently labeled species in the sample.

18. A method for distinguishing fluorescently labeled species at a single molecule level comprising:

providing pulsed illumination to an integrated chip;

the integrated chip comprising:

a plurality of analytical devices, each analytical device having a reaction cell, an optical element, and a detection element; wherein the optical element is in optical communication with the reaction cell and the detection element;

one or more integrated waveguides in optical communication with the reaction cells to deliver the pulsed illumination to the reaction cells;

a fluidic region in fluidic contact with the reaction cells, the fluidic region comprising a sample comprising multiple types of fluorescently labeled species;

whereby for each analytical device in the plurality of analytical devices, the pulsed illumination produces excitation events from the multiple types of fluorescently labeled species within the reaction cell, wherein an excitation event produces a signal at the detection element; and

distinguishing between the multiple types of fluorescently labeled species within the sample by correlating the timing of the signal at the detection element with the timing of the excitation event;

wherein each detection element comprises a plurality of storage elements;

wherein each respective storage element of the plurality of storage elements is turned off during intermediate stages of the illumination process to reduce noise contribution.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 1, 2019
From: MCCAFFREY, NATHANIEL JOSEPH; TURNER, STEPHEN; SAXENA, RAVI; HELGESEN, SCOTT EDWARD
To: PACIFIC BIOSCIENCES OF CALIFORNIA, INC.
Reel/Frame 049646/0744 →
Continuity (11)
Continuation 15786215 · Oct 17, 2017
Continuation 15272138 · Sep 21, 2016
Continuation 14730970 · Jun 4, 2015
Continuation 14477323 · Sep 4, 2014
Continuation 14107888 · Dec 16, 2013
Continuation 13895629 · May 16, 2013
Continuation 13031122 · Feb 18, 2011
Provisional Application 61306235 · Feb 19, 2010
Provisional Application 61387916 · Sep 29, 2010
Provisional Application 61410189 · Nov 4, 2010
Related Publication 20190309361A1 · Oct 10, 2019
Cited By (16)
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