DEVICES AND SYSTEMS FOR MOLECULAR BARCODING OF NUCLEIC ACID TARGETS IN SINGLE CELLS

• US 20160289669A1
• Filed: 01/22/2016
• Published: 10/06/2016
• Est. Priority Date: 01/22/2015
• Status: Abandoned Application

• Current Assignee: Becton, Dickinson & Co
• Original Assignee: Becton, Dickinson & Co
• Inventors: Fan, Christina, Chaney, Ari, Spuhler, Phillip, Li, Sixing, Huang, Xiaohua Chen, Metzler, Kimberly R., Walczak, Elisabeth Marie, Fodor, Stephen P.A., Fu, Glenn, Facer, Geoff, Stern, David, Lai, Janice
• Application Number:
  US15/004,618
• Publication Number:
  US 20160289669A1
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: B01L 2200/026 Fluid interfacing between devices or objects, e.g. connectors, inlet details
• CPC Class Codes: B01L 2200/0647 Handling flowable solids, e.g. microscopic beads, cells, particles
• CPC Class Codes: B01L 2300/06 Auxiliary integrated devices, integrated components
• CPC Class Codes: B01L 2300/0654 Lenses; Optical fibres
• CPC Class Codes: B01L 2300/0819 Microarrays; Biochips
• CPC Class Codes: B01L 2300/0877 Flow chambers
• CPC Class Codes: B01L 2300/12 Specific details about materials
• CPC Class Codes: B01L 2300/18 Means for temperature control
• CPC Class Codes: B01L 2400/082 Active control of flow resistance, e.g. flow controllers
• CPC Class Codes: B01L 3/502715 characterised by interfacing components, e.g. fluidic, electrical, optical or mechanical interfaces
• CPC Class Codes: B01L 3/502738 characterised by integrated valves microvalves F16K99/0001
• CPC Class Codes: B01L 3/502746 characterised by the means for controlling flow resistance, e.g. flow controllers, baffles B01L3/502738 takes precedence
• CPC Class Codes: B01L 3/502761 specially adapted for handling suspended solids or molecules independently from the bulk fluid flow, e.g. for trapping or sorting beads, for physically stretching molecules investigating characteristics of particles G01N15/00
• CPC Class Codes: C12N 15/1065 Preparation or screening of tagged libraries, e.g. tagged microorganisms by STM-mutagenesis, tagged polynucleotides, gene tags
• CPC Class Codes: C12Q 1/6846 Common amplification features
• CPC Class Codes: C12Q 1/6874 involving nucleic acid arrays, e.g. sequencing by hybridisation
• CPC Class Codes: C12Q 2521/107 RNA dependent DNA polymerase,(i.e. reverse transcriptase)
• CPC Class Codes: C12Q 2525/173 incorporating a polynucleotide run, e.g. polyAs, polyTs
• CPC Class Codes: C12Q 2525/185 incorporating bases where the precise position of the bases in the nucleic acid string is important
• CPC Class Codes: C12Q 2531/113 PCR
• CPC Class Codes: C12Q 2535/122 : Massive parallel sequencing
• CPC Class Codes: C12Q 2563/143 : Magnetism, e.g. magnetic label
• CPC Class Codes: C12Q 2563/149 : Particles, e.g. beads
• CPC Class Codes: G01N 35/0098 : involving analyte bound to insoluble magnetic carrier, e.g. using magnetic separation magnetic particles used in immunoassays G01N33/54326; magnetic separation in general B03C

Abstract

Disclosed herein are devices and systems comprising a) a substrate comprising at least 100 microwells and a plurality of beads, wherein a plurality of the at least 100 microwells each contain a single bead, and wherein the ratio of the average diameter of the microwells to the diameter of the beads ranges from about 1.2 to about 1.8; b) a flow cell in fluid communication with the substrate; and c) at least one inlet port and at least one outlet port, wherein the at least one inlet port and at least one outlet port are capable of directing a flow of a fluid through the flow cell, thereby contacting the microwells with the fluid.

Claims

1. (canceled)

2. A device comprising:

a substrate comprising at least 100 microwells, wherein each microwell has a volume ranging from about 1,000 μ

m³ to about 786,000 μ

m³, and wherein a surface of the at least 100 microwells is coated with a surface coating to improve wettability; and

a flow cell in fluid communication with the substrate.

7. The device of claim 2, further comprising at least one inlet port and at least one outlet port, wherein the at least one inlet port and the at least one outlet port are in fluid communication with the flow cell via fluid channels having axes that form an angle relative to the plane of the substrate, and wherein the at least one inlet port and the at least one outlet port are capable of directing a flow of a fluid through the flow cell, thereby contacting the microwells with the fluid.

9. The device of claim 2, wherein the substrate comprises from 1,000 to 5,000,000 microwells.

11. The device of claim 2, wherein each microwell has a volume ranging from about 21,000 μ

m³ to about 170,000 μ

m³.

13. The device of claim 2, wherein the microwells have a non-circular cross section in the plane of the substrate, and wherein the non-circular cross section in the plane of the substrate is square or hexagonal.

14. The device of claim 2, wherein the aspect ratio of average diameter to depth for the at least 100 microwells ranges from about 0.1 to 2.

16. The device of claim 2, wherein the dimension of each microwell allows each microwell to contain at most one bead.

17. The device of claim 2, wherein the ratio of the average diameter of the microwells to the diameter of the beads ranges from about 1.2 to about 1.8.

18. The device of claim 2, wherein the side walls of the microwells have a positive draft angle of about 1 to 15 degrees.

20. The device of claim 2, wherein the substrate further comprises surface features that surround each microwell or straddle the surface between microwells of the at least 100 microwells.

21. The device of claim 20, wherein the substrate further comprises surface features that surround each microwell or straddle the surface between microwells of the at least 100 microwells, wherein the surface features are selected from the group consisting of rounded, domed, ridged, and peaked surface features, or any combination thereof.

22. The device of claim 2, wherein the percentage of the at least 100 microwells that contain a single bead is at least about 10%.

24. The device of claim 2, wherein the percentage of the at least 100 microwells that contain a single cell is between about 0.01% and about 15%.

26. The device of claim 2, wherein a surface of the at least 100 microwells is coated with polyethylene glycol (PEG), poly-Hema, pluronic acid F68, pluronic acid F108, polysorbate 20, silicon dioxide (SiO2), or any combination thereof.

27. The device of claim 2, wherein a surface of the at least 100 microwells comprises a plasma-treated surface.

33. The device of claim 2, wherein the substrate is fabricated from a material selected from the group consisting of silicon, fused-silica, glass, a polymer, a metal, an elastomer, polydimethylsiloxane, agarose, and a hydrogel, or any combination thereof.

36. The device of claim 2, wherein the flow cell is fabricated from a material selected from the group consisting of silicon, fused-silica, glass, polydimethylsiloxane (PDMS;

elastomer), polymethylmethacrylate (PMMA), polycarbonate (PC), polypropylene (PP), polyethylene (PE), high density polyethylene (HDPE), polyimide, cyclic olefin polymers (COP), cyclic olefin copolymers (COC), polyethylene terephthalate (PET), epoxy resin, and metal, or any combination of these materials.

40. The device of claim 2, further comprising a pipette tip interface for loading or removing samples, assay reagents, bead suspensions, or waste from the device.

41. The device of claim 40, wherein the pipette tip interface comprises a conical feature that mates to a pipette tip to form a fluid connection with the inlet port or outlet port.

42. The device of claim 41, wherein the conical feature is comprised of a compliant material that forms a substantially leak-proof seal with the pipette tip.

44. The device of claim 41, further comprising a valve that prevents fluid flow within the device unless a pipette tip is inserted into the conical feature of the pipette tip interface.

45. The device of claim 2, wherein each single bead of a plurality of beads contained within the at least 100 microwells comprises a plurality of tethered stochastic labels capable of attaching to a target nucleic acid molecule in a stochastic manner, wherein each stochastic label in the plurality of tethered stochastic labels comprises a cell label that is identical for all of the stochastic labels attached to that bead, but is different for stochastic labels attached to different beads, wherein the plurality of tethered stochastic labels attached to a single bead further comprises a diverse set of molecular labels, and wherein each stochastic label in the plurality of tethered stochastic labels further comprises a target nucleic acid molecule binding region.

3. (canceled)

4. (canceled)

5. (canceled)

6. (canceled)

8. (canceled)

10. (canceled)

12. (canceled)

15. (canceled)

19. (canceled)

23. (canceled)

25. (canceled)

28. (canceled)

29. (canceled)

30. (canceled)

31. (canceled)

32. (canceled)

34. (canceled)

35. (canceled)

37. (canceled)

38. (canceled)

39. (canceled)

43. (canceled)

46-51. -51. (canceled)

52. A system comprising:

a device comprising;

a substrate comprising at least 100 microwells, wherein each microwell has a volume ranging from about 1,000 μ

m³ to about 786,000 μ

m³, and wherein a surface of the at least 100 microwells is coated with a surface coating to improve wettability;

a flow cell in fluid communication with the substrate; and

at least one inlet port and at least one outlet port, wherein the at least one inlet port and at least one outlet port are capable of directing a flow of a fluid through the flow cell, thereby contacting the microwells with the fluid; and

a flow controller;

wherein the flow controller is configured to control the delivery of fluids.

54. The system of claim 52, further comprising fluids wherein the fluids comprise cell samples, bead suspensions, assay reagents, or any combination thereof.

56. The system of claim 54, wherein cell samples and bead suspensions are dispensed or injected directly into the device by the user.

57. The system of claim 54, wherein beads and assay reagents other than cell samples are preloaded in the device.

58. The system of claim 52, wherein the flow controller is configured to intersperse fluid injections into the flow cell with air injections.

59. The system of claim 52, further comprising:

a distribution mechanism for enhancing the uniform distribution of cells and beads across the at least 100 microwells, wherein the distribution mechanism performs an action selected from the group consisting of rocking, shaking, swirling, recirculating flow, low frequency agitation, and high frequency agitation, or any combination thereof;

a cell lysis mechanism that uses a high frequency piezoelectric transducer for sonicating the cells;

comprising a temperature controller for maintaining a user-specified temperature, or for ramping temperature between two or more specified temperatures over two or more specified time intervals;

a magnetic field controller for creating magnetic field gradients used in eluting beads from the at least 100 microwells or for transporting beads through the device;

an imaging system configured to capture and process images of all or a portion of the at least 100 microwells, wherein the imaging system further comprises an illumination subsystem, an imaging subsystem, and a processor; and

a selection mechanism, wherein information derived from the processed images is used to identify a subset of cells exhibiting one or more specified characteristics, and the selection mechanism is configured to either include or exclude the subset of cells from subsequent data analysis.

53. (canceled)

55. (canceled)

60-113. -113. (canceled)

114. A method for loading one or more cell samples into microwells of a device, wherein the device comprises:

a substrate comprising at least 100 microwells, wherein each microwell has a volume ranging from about 1,000 μ

m³ to about 786,000 μ

m³, and wherein a surface of the at least 100 microwells is coated with a surface coating to improve wettability; and

a flow cell in fluid communication with the substrate,

the method comprising;

injecting air into the flow cell in fluid communication with the substrate comprising at least 100 microwells;

injecting a cell sample into the flow cell; and

injecting air into the flow cell.

115. The method of claim 114, further comprising injecting a buffer or bead suspension into the flow cell following injecting a cell sample into the flow cell.

116-163. -163. (canceled)