Quantitative amplification and detection of small numbers of target polynucleotides

• US 20050208539A1
• Filed: 12/30/2004
• Published: 09/22/2005
• Est. Priority Date: 12/31/2003
• Status: Abandoned Application

• Current Assignee: Applied Biosystems LLC (Thermo Fisher Scientific Incorporated)
• Original Assignee: Applied Biosystems LLC (Thermo Fisher Scientific Incorporated)
• Inventors: Lehto, Dennis, Vann, Charles S., Reed, Mark, Lao, Kai Qin, Stern, Seth R.
• Application Number:
  US11/026,924
• Publication Number:
  US 20050208539A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: B01L 2300/0861 Configuration of multiple channels and/or chambers in a single devices
• CPC Class Codes: B01L 2300/18 Means for temperature control
• CPC Class Codes: B01L 2400/06 Valves, specific forms thereof
• CPC Class Codes: B01L 3/502707 characterised by the manufacture of the container or its components by shaping or joining plastic parts B29C59/00, B29C65/00; by laminating B32B37/00; manufacture of microstructural devices in general B81C
• CPC Class Codes: B01L 3/502715 characterised by interfacing components, e.g. fluidic, electrical, optical or mechanical interfaces
• CPC Class Codes: B01L 7/52 with provision for submitting samples to a predetermined sequence of different temperatures, e.g. for treating nucleic acid samples amplification or hybridisation processes per se C12Q1/68; controlling sequential reactions for synthesis B01J19/0046
• CPC Class Codes: C12Q 1/686 Polymerase chain reaction [PCR]
• CPC Class Codes: C12Q 2527/125 Specific component of sample, medium or buffer

Abstract

Devices, assemblies, systems and methods described herein enable detection of as few as a single copy of a target nucleic acid molecule. Polynucleotides copied from a single or a small number of target nucleotide(s) within regions near to an initial copying site may be detected by optical or other methods as disclosed herein. Devices, assemblies and systems may comprise probes and/or primer molecules. Systems comprising optical assemblies, thermal assemblies and reaction assemblies (having reaction chambers for amplification of target nucleic acid molecules) are provided in which used reaction assemblies may be replaced to provide reusable devices. Systems comprising analytical assemblies and detection assemblies are provided in which an assay cartridge having assay chambers may engage a thermal assembly for amplification of target nucleic acid molecules. These devices, systems and methods offer the advantages of detection of as few as a single copy of a target nucleic acid molecule.

Claims

1. A device for amplifying and/or detecting at least one nucleic acid molecule in a sample, comprising:

a first well region configured to receive probe molecules and primer molecules, said probe molecules and said primer molecules each configured to hybridize with at least a portion of a target nucleic acid molecule;

a second well region configured to receive target nucleic acid molecules; and

a connecting region providing a restricted pathway connecting said first well region and said second well region;

said restricted pathway comprising an elongated channel configured to direct the flow of a liquid by capillary action and being effective to allow contact between said probe molecules, said primer molecules, and said target nucleic acid molecules so that at least one target nucleic acid molecule may be amplified and/or detected.

2. The device of claim 1, wherein said elongated channel has a width of less than about 2 mm and a depth of less than about 0.5 mm.

3. The device of claim 1, wherein said elongated channel has a width of about 0.3 mm and a depth of about 0.15 mm.

4. The device of claim 1, comprising a plurality of first well regions and a plurality of connecting regions.

5. The device of claim 1, wherein a connecting region comprises dried probe or primer molecules.

6. The device of claim 1, further comprising a valve connecting a first well region and a connecting region.

7. The device of claim 1, further comprising a divider configured to segment said connecting region, wherein said divider may be situated in place after said target nucleic acid molecules have been added to said second well region effective to separate said connecting region into a plurality of wells.

8. A device for amplifying and/or detecting at least one nucleic acid molecule in a sample, comprising:

a well having an interior region comprising a well base and configured to receive probe molecules, primer molecules, and target nucleic acid molecules, said probe molecules and said primer molecules each configured to hybridize with at least a portion of a target nucleic acid molecule;

said well base being transparent or translucent to radiation of at least a portion of the electromagnetic spectrum, having a plurality of base locations and comprising a thin gel layer having an area and configured to accept said probe, primer and target molecules effective to diffuse at least some of said probe, primer and target molecules into said thin gel layer to disperse said target molecules to different locations so that at a given location within the thin gel layer a target nucleic acid molecule may be contacted by probe molecules and primer molecules so that a target molecule may be amplified and/or detected at a given location.

9. The device of claim 8, comprising a plurality of wells.

10. The device of claim 8, wherein said target nucleic acid molecules disperse within said thin gel layer at a density of less than about 1 target nucleic acid molecules per square millimeter as viewed from above.

11. The device of claim 8, wherein said thin gel layer comprises a gel material selected from the group of gel materials consisting of gelatin, agar, agarose, acrylamide, Sepharose®

, Sephadex®

, Sephacryl®

, casein, unfixed gels and cross-linked gels.

12. The device of claim 8, wherein said thin gel layer comprises a gel layer having a thickness of less than about 0.1 mm.

13. A device for amplifying and/or detecting at least one nucleic acid molecule in a sample, comprising:

a well having an interior volume comprising a gel and configured to receive probe molecules, primer molecules, and target nucleic acid molecules, said probe molecules and said primer molecules each configured to hybridize with at least a portion of a target nucleic acid molecule; and

a well base transparent or translucent to radiation of at least a portion of the electromagnetic spectrum;

said gel being configured so that at least some of said probe, primer and target molecules may diffuse into said gel to disperse said target molecules to different locations within said interior volume so that at a given location within the gel a target nucleic acid molecule may be contacted by probe molecules and primer molecules effective that a target molecule may be amplified and/or detected at a given location.

14. The device of claim 13, comprising a plurality of wells.

15. The device of claims 13, wherein said gel comprises a gel material selected from the group of gel materials consisting of gelatin, agar, agarose, acrylamide, Sepharose®

, Sephadex®

, Sephacryl®

, casein, unfixed gels and cross-linked gels.

16. The device of claim 13, wherein said target nucleic acid molecules disperse into a volume at a density of less than about 10 target nucleic acid molecules per cubic millimeter.

17. A device for amplifying and/or detecting at least one nucleic acid molecule in a sample, comprising:

a plurality of hydrophilic wells separated from each other by a hydrophobic surface and each having an interior surface comprising probe molecules and/or primer molecules, said probe molecules and said primer molecules each configured to hybridize with at least a portion of a target nucleic acid molecule;

said plurality of wells being sized and spaced to receive target nucleic acid molecules for contact with probe molecules and primer molecules within a single well effective that a target nucleic acid molecule may be amplified and/or detected within a single well.

18. The device of claim 17, wherein said hydrophobic surface comprises an elongated post with an end, said end having a hydrophobic surface and having a plurality of depressions in said end comprising said plurality of hydrophilic wells.

19. The device of claim 18, wherein said depressions comprising said plurality of hydrophilic wells have depths of less than about 2 mm and widths of less than about 5 mm.

20. The device of claim 18, comprising a plurality of fiber optic bundles.

21. A device for amplifying and/or detecting at least one nucleic acid molecule in a sample, comprising:

a substrate having a substantially planar hydrophobic surface, a plurality of walls disposed on and substantially perpendicular to said surface, said walls defining a plurality of wells, said wells having a hydrophilic surface defining at least in part a volume configured to receive probe molecules, primer molecules, and target nucleic acid molecules, said probe molecules and said primer molecules each configured to hybridize with at least a portion of a target nucleic acid molecule effective that a target nucleic acid molecule may be amplified and/or detected within a depression.

22. The device of claim 21, wherein said wells comprise probe and/or primer molecules, each of said probe and/or primer molecules being configured to hybridize with at least a portion of a target nucleic acid molecule.

23. The device of claim 21, wherein said plurality of wells have depths of less than about 1 mm and widths of less than about 2 mm.

24. The device of claim 22, wherein said plurality of wells have depths of less than about 1 mm and widths of less than about 2 mm.

25. A method for amplifying and/or detecting at least one nucleic acid molecule in a sample, comprising:

contacting a first solution comprising a primer molecule and/or a probe molecule with a channel configured to conduct a solution along said channel, said probe molecules and said primer molecules each configured to hybridize with at least a portion of a target nucleic acid molecule;

drying said first solution effective that said primer and/or probe molecules is/are retained within said channel;

contacting a second solution comprising a target nucleic acid molecule with said channel configured to conduct a solution along said channel, effective to mix said target nucleic acid molecule, said dried probe and/or said primer molecules into said second solution within said channel at an initial temperature, wherein probes are cleaved by extending primers to generate fluorescence around targets that match the probes;

applying heat effective to raise the temperature of the mixed target nucleic acid, probe and primer molecules to a raised temperature above said initial temperature;

allowing the temperature to become reduced effective to reduce the temperature of the mixed target nucleic acid, probe and primer molecules from said raised temperature to a temperature closer to said initial temperature, said raising of temperature and allowing temperature to become reduced comprising a thermal cycle;

repeating said thermal cycle effective to produce nucleic acid copies of said target nucleic acid molecule effective to amplify and/or detect said target nucleic acid molecule.

26. The method of claim 25, wherein said thermal cycle is repeated after a short interval of time effective to prevent diffusion of said copies of said target nucleic acid molecules greater than a short distance from said individual target nucleic acid molecules, wherein said thermal cycles are repeated a number of times comprising no more than about twenty cycles.

27. The method of claim 25, wherein said conduction of solution along said channel comprises capillary action.

28. The method of claim 25, wherein said target nucleic acid molecule is detected by detection of an optical signal related to the presence of either said target nucleic acid molecule or of a copy of said target nucleic acid molecule.

29. The method of claim 25, wherein said contacting a solution with a channel comprises opening a valve.

30. A method for amplifying and/or detecting at least one nucleic acid molecule in a sample, comprising:

contacting a solution comprising a primer molecule and a probe molecule with a plurality of gel regions, said plurality of gel regions being disposed within a plurality of wells, each well comprising a gel region, said wells separated from other wells by barriers disposed between said wells, said probe and said primer molecules each configured to hybridize with at least a portion of a target nucleic acid molecule;

allowing at least some of said primer molecules and said probe molecules to diffuse into said gel;

contacting said gel with a second solution comprising a target nucleic acid molecule, effective to mix said target nucleic acid molecule with probe and primer molecules within said gel at an initial temperature, wherein said probes are cleaved by extending primers to generate fluorescence around targets that match the probes;

applying heat effective to raise the temperature of the mixed target nucleic acid, probe and primer molecules to a raised temperature above said initial temperature;

allowing the temperature to become reduced effective to reduce the temperature of the mixed target nucleic acid, probe and primer molecules from said raised temperature to a temperature closer to said initial temperature, said raising and allowing the temperature to become reduced comprising a thermal cycle;

repeating said thermal cycle effective to produce nucleic acid copies of said target nucleic acid molecule effective to amplify and/or detect said target nucleic acid molecule.

31. The method of claim 30, wherein said gel regions comprise thin gel layers having a thickness of less than about 0.1 mm.

32. The method of claim 30, wherein said thermal cycles are repeated after a short interval of time effective to prevent diffusion of said copies of said target nucleic acid molecules greater than a short distance from said individual target nucleic acid molecules, wherein the number of said thermal cycles comprises fewer than about twenty thermal cycles.

33. A method for amplifying and/or detecting at least one nucleic acid molecule in a sample, comprising:

placing a hydrophilic well in contact with a solution, said hydrophilic well comprising at least a portion of a device comprising a hydrophilic well surrounded by a hydrophobic surface, said solution comprising a target nucleic acid molecule, a primer molecule and a probe molecule, said probe molecules and said primer molecules each configured to hybridize with at least a portion of said target nucleic acid molecule;

removing said hydrophilic well from contact with said solution effective that a portion of said solution remains in contact with said hydrophilic well and substantially no solution remains in contact with said hydrophobic surface;

placing at least a portion of said device in contact with a hydrophobic liquid, said portion comprising at least a portion of said hydrophobic surface surrounding a well, effective that said solution in contact with said hydrophilic well remains in contact with said well;

applying heat effective to raise the temperature of the mixed target nucleic acid, probe and primer molecules from an initial temperature to a raised temperature above said initial temperature;

allowing the temperature to become reduced effective to reduce the temperature of the mixed target nucleic acid, probe and primer molecules from said raised temperature to a temperature closer to said initial temperature, said raising and said allowing the temperature to become reduced comprising a thermal cycle;

repeating said thermal cycle effective to produce nucleic acid copies of said target nucleic acid molecule effective to amplify said target nucleic acid molecule; and

detecting the presence of said target nucleic acid molecule or copies thereof.

34. A method for amplifying and/or detecting at least one nucleic acid molecule in a sample, comprising:

contacting a portion of a substrate comprising a hydrophilic well surrounded by a hydrophobic surface with a first solution, said first solution comprising a primer molecule and a probe molecule, said probe molecules and said primer molecules each configured to hybridize with at least a portion of a target nucleic acid molecule;

drying at least a portion of said substrate effective that said probe molecules and said primer molecules dry into at least a portion of said hydrophilic well;

contacting said hydrophilic well with a volume of a second solution comprising said target nucleic acid molecule;

removing said well from contact with said volume of said second solution, effective that a mixture of said target nucleic acid molecule, said probe and said primer remains in said second solution in contact with said well;

placing at least a portion of said substrate into contact with a hydrophobic liquid, effective that said mixture remains in contact with said well;

making copies of said target nucleic acid molecule within or adjacent said mixture; and

detecting the presence of said target nucleic acid molecule or copies thereof.

35. The method of claim 34, wherein said making copies comprises:

applying heat effective to raise the temperature of said mixture comprising target nucleic acid, probe and primer molecules from an initial temperature to a raised temperature above said initial temperature;

allowing the temperature to become reduced effective to reduce the temperature of said mixture from said raised temperature to a temperature closer to said initial temperature, said raising and said allowing the temperature to become reduced comprising a thermal cycle; and

repeating said thermal cycle effective to produce nucleic acid copies of said target nucleic acid molecule effective to amplify and/or detect said target nucleic acid molecule.

36. The method of claim 35, the method further comprising subjecting said mixture to a thermal cycle without substantial evaporation of fluid from said mixture.

37. A system for amplifying and/or detecting at least one nucleic acid molecule in a sample, comprising a plurality of assemblies, each of said assemblies configured for use with at least one other of said assemblies, comprising:

an optical assembly comprising an aperture and optical apparatus selected from a lens, a filter, and a window;

a reaction assembly comprising a reaction chamber configured for receiving a solution comprising a sample containing a target nucleic acid molecule and for reacting said sample with a primer molecule and a probe molecule in said reaction chamber; and

a thermal assembly configured to receive said reaction assembly, comprising a thermal cycling device capable of providing heat to said reaction assembly when said reaction assembly is received by said thermal assembly, and a controller configured for controlling the heat provided by said thermal cycling device.

38. The system of claim 37, wherein said reaction assembly further comprises a window, a support, a septum covering a port, and a filter separating said port from said reaction chamber effective to allow passage of a target nucleic acid molecule from said port to said reaction chamber while substantially preventing passage of cellular debris.

39. The system of claim 37, configured for use with a plurality of reaction assemblies, wherein said system is configured for use with a first reaction assembly or a second reaction assembly, and wherein said first reaction assembly may be replaced with said second reaction assembly.

40. The system of claim 37, wherein said reaction assembly comprises dried probe and/or primer molecules.

41. The system of claim 37, wherein said reaction assembly further comprises a plurality of electrodes effective for electrophoresing a target nucleic acid molecule upon provision of electrical power to said electrodes.

42. The system of claim 37, wherein said reaction assembly comprises a plurality of chambers.

43. The system of claim 41, wherein said reaction assembly comprises a plurality of chambers and wherein said plurality of electrodes is effective for electrophoresing a target nucleic acid molecule from one chamber to another chamber of said reaction assembly upon provision of electrical power to said electrodes.

44. The system of claim 37, wherein said reaction assembly further comprises a matrix effective to substantially prevent passage of cellular debris between chambers in said reaction assembly.

45. The system of claim 37, wherein said reaction assembly further comprises a matrix suitable for separation of cellular elements.

46. The system of claim 37, further comprising a light source.

47. The system of claim 37, further comprising a valve effective to regulate passage of material between chambers in said reaction assembly.

48. The system of claim 37, wherein said reaction assembly comprises dried probe or primer molecules.

49. The system of claim 43, wherein said reaction assembly comprises dried probe or primer molecules.

50. The system of claim 37, wherein said reaction assembly comprises a sample preparation module, at least one assay chamber configured for amplifying nucleic acid molecules therein, and a pathway configured to allow passage of fluid from said sample preparation module to said at least one assay chamber.

51. The system of claim 43, wherein said electrodes are configured to provide a first voltage gradient and a second voltage gradient, wherein said first voltage gradient has a first polarity, and said second voltage gradient has a second polarity, and wherein said first polarity and said second polarity are different.

52. The system of claim 51, wherein said first polarity of said first voltage gradient is perpendicular to said second polarity of said second voltage gradient.

53. The system of claim 51, wherein said electrodes are configured to provide said first voltage gradient at a different time than said second voltage gradient is provided.

54. The system of claim 51, wherein said reaction chamber comprises a matrix suitable for separation of cellular elements.