Unimolecular segment amplification and sequencing

• US 6,632,609 B2
• Filed: 04/24/2001
• Issued: 10/14/2003
• Est. Priority Date: 11/21/1995
• Status: Expired due to Term

• Current Assignee: Yale University
• Original Assignee: Yale University
• Inventors: Lizardi, Paul M.
• Primary Examiner(s): WHISENANT, ETHAN C
• Application Number:
  US09/841,513
• Publication Number:
  US 20020192649A1
• Time in Patent Office: 903 Days
• Field of Search: 435/6, 435/7.1, 435/91.2, 536/23.1, 536/24.3
• US Class Current: 435/6.12
• CPC Class Codes: C12Q 1/6804 Nucleic acid analysis using immunogens immunoassay G01N33/53
• CPC Class Codes: C12Q 1/6809 Methods for determination or identification of nucleic acids involving differential detection
• CPC Class Codes: C12Q 1/6816 characterised by the detection means C12Q1/6804 takes precedence
• CPC Class Codes: C12Q 1/6844 Nucleic acid amplification reactions
• CPC Class Codes: C12Q 1/6853 using modified primers or templates
• CPC Class Codes: C12Q 1/6862 Ligase chain reaction [LCR]
• CPC Class Codes: C12Q 2525/161 incorporating target specific and non-target specific sites
• CPC Class Codes: C12Q 2525/307 Circular oligonucleotides
• CPC Class Codes: C12Q 2531/119 Strand displacement amplification [SDA]
• CPC Class Codes: C12Q 2531/125 Rolling circle
• CPC Class Codes: C12Q 2531/143 Promoter based amplification, e.g. NASBA, 3SR, TAS
• CPC Class Codes: C12Q 2537/125 Sandwich assay format
• CPC Class Codes: C12Q 2537/143 Multiplexing, i.e. use of multiple primers or probes in a single reaction, usually for simultaneously analyse of multiple analysis
• CPC Class Codes: C12Q 2539/113 Differential Display Analysis [DDA]
• CPC Class Codes: C12Q 2563/131 the label being a member of a cognate binding pair, i.e. extends to antibodies, haptens, avidin
• CPC Class Codes: C12Q 2563/179 the label being a nucleic acid
• CPC Class Codes: C12Q 2565/102 Multiple non-interacting labels

Abstract

Disclosed are compositions and a method for amplification of and multiplex detection of molecules of interest involving rolling circle replication. The method is useful for simultaneously detecting multiple specific nucleic acids in a sample with high specificity and sensitivity. The method also has an inherently low level of background signal. A preferred form of the method consists of an association operation, an amplification operation, and a detection operation. The association operation involves association of one or more specially designed probe molecules, either wholly or partly nucleic acid, to target molecules of interest. This operation associates the probe molecules to a target molecules present in a sample. The amplification operation is rolling circle replication of circular nucleic acid molecules, termed amplification target circles, that are either a part of, or hybridized to, the probe molecules. A single round of amplification using rolling circle replication results in a large amplification of the amplification target circles. Following rolling circle replication, the amplified sequences are detected using combinatorial multicolor coding probes that allow separate, simultaneous, and quantitative detection of multiple different amplified target circles representing multiple different target molecules. Since the amplified product is directly proportional to the amount of target sequence present in a sample, quantitative measurements reliably represent the amount of a target sequence in a sample. Major advantages of this method are that a large number of distinct target molecules can be detected simultaneously, and that differences in the amounts of the various target molecules in a sample can be accurately quantified. It is also advantageous that the DNA replication step is isothermal, and that signals are strictly quantitative because the amplification reaction is linear and is catalyzed by a highly processive enzyme.

Claims

1. A method for detecting proteins, the method comprising

an amplification operation,

wherein a rolling circle replication primer is coupled to a specific binding molecule, wherein the specific binding molecule can interact with a target molecule, wherein the target molecule is a protein,

wherein the amplification operation comprises rolling circle replication of an amplification target circle to produce tandem sequence DNA.

2. The method of claim 1 wherein the specific binding molecule is bound to a target molecule.

3. The method of claim 1 further comprising bringing the specific binding molecule into contact with the target molecule.

4. The method of claim 1 wherein the method includes a step of bringing the specific binding molecule into contact with the target molecule.

5. The method of claim 1 wherein the specific binding molecule is an antibody.

6. The method of claim 1 wherein rolling circle replication of the amplification target circle is primed by the rolling circle replication primer.

7. The method of claim 1 wherein the amplification operation produces tandem sequence DNA and secondary tandem sequence DNA, wherein the method further comprises detecting the tandem sequence DNA, the secondary tandem sequence DNA, or both.

8. The method of claim 1 wherein a plurality of different rolling circle replication primers are used in the amplification operation.

9. The method of claim 8 wherein the rolling circle replication primers are each coupled to a different specific binding molecule.

10. The method of claim 9 wherein the different specific binding molecules each interacts with a different target molecule.

11. A method of detecting proteins, the method comprising,

(a) mixing a specific binding molecule with a target sample comprising a target molecule wherein a rolling circle replication primer is coupled to the specific binding molecule, wherein the specific binding molecule binds to the target molecule,

wherein the target molecule is a protein,

(b) mixing the rolling circle replication primer with an amplification target circle, to produce a primer-ATC mixture, and incubating the primer-ATC mixture under conditions that promote hybridization between the amplification target circle and the rolling circle replication primer in the primer-ATC mixture,

wherein the amplification target circle comprises a single-stranded, circular DNA molecule comprising a primer complement portion, wherein the primer complement portion is complementary to the rolling circle replication primer, and

(c) mixing DNA polymerase with the primer-ATC mixture, to produce a polymerase-ATC mixture, and incubating the polymerase-ATC mixture under conditions that promote replication of the amplification target circle,

wherein replication of the amplification target circle results in the formation of tandem sequence DNA.

12. A method for detecting proteins, the method comprising

an amplification operation,

wherein an amplification target circle is coupled to a specific binding molecule, wherein the specific binding molecule can interact with a target molecule, wherein the target molecule is a protein,

wherein the amplification operation comprises rolling circle replication of the amplification target circle to produce tandem sequence DNA.

13. The method of claim 12 wherein the specific binding molecule is bound to a target molecule.

14. The method of claim 12 further comprising bringing the specific binding molecule into contact with the target molecule.

15. The method of claim 12 wherein the method includes a step of bringing the specific binding molecule into contact with the target molecule.

16. The method of claim 12 wherein the specific binding molecule is an antibody.

17. The method of claim 12 wherein amplification target circle is tethered to the specific binding molecule so that the amplification target circle can rotate freely.

18. The method of claim 12 wherein the amplification operation produces tandem sequence DNA and secondary tandem sequence DNA, wherein the method further comprises detecting the tandem sequence DNA, the secondary tandem sequence DNA, or both.

19. The method of claim 12 wherein a plurality of different amplification target circles are used in the amplification operation.

20. The method of claim 19 wherein the rolling circle replication primers are each coupled to a different specific binding molecule.

21. The method of claim 20 wherein the different specific binding molecules each interacts with a different target molecule.

22. A method of detecting proteins, the method comprising,

(a) mixing a specific binding molecule with a target sample comprising a target molecule wherein an amplification target circle is coupled to the specific binding molecule, wherein the specific binding molecule binds to the target molecule,

wherein the target molecule is a protein,

(b) mixing a rolling circle replication primer with the amplification target circle, to produce a primer-ATC mixture, and incubating the primer-ATC mixture under conditions that promote hybridization between the amplification target circle and the rolling circle replication primer in the primer-ATC mixture,

wherein the amplification target circle comprises a single-stranded, circular DNA molecule comprising a primer complement portion, wherein the primer complement portion is complementary to the rolling circle replication primer, and

(c) mixing DNA polymerase with the primer-ATC mixture, to produce a polymerase-ATC mixture, and incubating the polymerase-ATC mixture under conditions that promote replication of the amplification target circle,

wherein replication of the amplification target circle results in the formation of tandem sequence DNA.

23. A method for detecting proteins, the method comprising

a DNA ligation operation and an amplification operation,

wherein the DNA ligation operation comprises circularization of an open circle probe, wherein circularization of the open circle probe is dependent on hybridization of the open circle probe to a target sequence, wherein the target sequence is coupled to a specific binding molecule, wherein the specific binding molecule can interact with a target molecule, wherein the target molecule is a protein,

wherein the amplification operation comprises rolling circle replication of the circularized open circle probe to produce tandem sequence DNA.

24. The method of claim 23 wherein the specific binding molecule is bound to a target molecule.

25. The method of claim 23 further comprising bringing the specific binding molecule into contact with the target molecule.

26. The method of claim 23 wherein the method includes a step of bringing the specific binding molecule into contact with the target molecule.

27. The method of claim 23 wherein the amplification operation produces tandem sequence DNA and secondary tandem sequence DNA, wherein the method further comprises detecting the tandem sequence DNA, the secondary tandem sequence DNA, or both.

28. The method of claim 23 wherein a plurality of different target sequences are used in the amplification operation.

29. The method of claim 28 wherein the rolling circle replication primers are each coupled to a different specific binding molecule.

30. The method of claim 29 wherein the different specific binding molecules each interacts with a different target molecule.

31. A method of detecting proteins, the method comprising,

(a) mixing a specific binding molecule with a target sample comprising a target molecule wherein a target sequence is coupled to the specific binding molecule, wherein the specific binding molecule binds to the target molecule,

wherein the target molecule is a protein,

(b) mixing an open circle probe with the target sample, to produce an OCP-target sample mixture, and incubating the OCP-target sample mixture under conditions that promote hybridization between the open circle probe and the target sequence in the OCP-target sample mixture,

(c) mixing ligase with the OCP-target sample mixture, to produce a ligation mixture, and incubating the ligation mixture under conditions that promote ligation of the open circle probe to form an amplification target circle,

(d) mixing a rolling circle replication primer with the ligation mixture, to produce a primer-ATC mixture, and incubating the primer-ATC mixture under conditions that promote hybridization between the amplification target circle and the rolling circle replication primer in the primer-ATC mixture, and

(e) mixing DNA polymerase with the primer-ATC mixture, to produce a polymerase-ATC mixture, and incubating the polymerase-ATC mixture under conditions that promote replication of the amplification target circle,

wherein replication of the amplification target circle results in the formation of tandem sequence DNA.

32. A method comprising

an amplification operation,

wherein a nucleic acid tag is coupled to a specific binding molecule, wherein the specific binding molecule can interact with a target molecule, wherein the target molecule is a protein,

wherein the amplification operation comprises rolling circle replication of an amplification target circle to produce tandem sequence DNA.

33. The method of claim 32 wherein the specific binding molecule is bound to a target molecule.

34. The method of claim 32 further comprising bringing the specific binding molecule into contact with the target molecule.

35. The method of claim 32 wherein the method includes a step of bringing the specific binding molecule into contact with the target molecule.

36. A method for detecting nucleic acid molecules, the method comprising

an amplification operation,

wherein a rolling circle replication primer is coupled to a specific binding molecule, wherein the specific binding molecule can interact with a target molecule, wherein the target molecule is a nucleic acid molecule,

wherein the amplification operation comprises rolling circle replication of an amplification target circle to produce tandem sequence DNA.

37. The method of claim 36 wherein the specific binding molecule is bound to a target molecule.

38. The method of claim 36 further comprising bringing the specific binding molecule into contact with the target molecule.

39. The method of claim 36 wherein the method includes a step of bringing the specific binding molecule into contact with the target molecule.

40. The method of claim 36 wherein rolling circle replication of the amplification target circle is primed by the rolling circle replication primer.

41. The method of claim 36 wherein the amplification operation produces tandem sequence DNA and secondary tandem sequence DNA, wherein the method further comprises detecting the tandem sequence DNA, the secondary tandem sequence DNA, or both.

42. The method of claim 36 wherein a plurality of different rolling circle replication primers are used in the amplification operation.

43. The method of claim 42 wherein the rolling circle replication primers are each coupled to a different specific binding molecule.

44. The method of claim 43 wherein the different specific binding molecules each interacts with a different target molecule.

45. A method of detecting nucleic acid molecules, the method comprising,

(a) mixing a specific binding molecule with a target sample comprising a target molecule wherein a rolling circle replication primer is coupled to the specific binding molecule, wherein the specific binding molecule binds to the target molecule,

wherein the target molecule is a nucleic acid molecule,

(b) mixing the rolling circle replication primer with an amplification target circle, to produce a primer-ATC mixture, and incubating the primer-ATC mixture under conditions that promote hybridization between the amplification target circle and the rolling circle replication primer in the primer-ATC mixture,

wherein the amplification target circle comprises a single-stranded, circular DNA molecule comprising a primer complement portion, wherein the primer complement portion is complementary to the rolling circle replication primer, and

(c) mixing DNA polymerase with the primer-ATC mixture, to produce a polymerase-ATC mixture, and incubating the polymerase-ATC mixture under conditions that promote replication of the amplification target circle,

wherein replication of the amplification target circle results in the formation of tandem sequence DNA.

46. A method for detecting nucleic acid molecules, the method comprising

an amplification operation,

wherein an amplification target circle is coupled to a specific binding molecule, wherein the specific binding molecule can interact with a target molecule, wherein the target molecule is a nucleic acid molecule,

wherein the amplification operation comprises rolling circle replication of the amplification target circle to produce tandem sequence DNA.

47. The method of claim 46 wherein the specific binding molecule is bound to a target molecule.

48. The method of claim 46 further comprising bringing the specific binding molecule into contact with the target molecule.

49. The method of claim 46 wherein the method includes a step of bringing the specific binding molecule into contact with the target molecule.

50. The method of claim 46 wherein amplification target circle is tethered to the specific binding molecule so that the amplification target circle can rotate freely.

51. The method of claim 46 wherein the amplification operation produces tandem sequence DNA and secondary tandem sequence DNA, wherein the method further comprises detecting the tandem sequence DNA, the secondary tandem sequence DNA, or both.

52. The method of claim 46 wherein a plurality of different amplification target circles are used in the amplification operation.

53. The method of claim 52 wherein the rolling circle replication primers are each coupled to a different specific binding molecule.

54. The method of claim 53 wherein the different specific binding molecules each interacts with a different target molecule.

55. A method of detecting nucleic acid molecules, the method comprising,

(a) mixing a specific binding molecule with a target sample comprising a target molecule wherein an amplification target circle is coupled to the specific binding molecule, wherein the specific binding molecule binds to the target molecule,

wherein the target molecule is a nucleic acid molecule,

(b) mixing the rolling circle replication primer with an amplification target circle, to produce a primer-ATC mixture, and incubating the primer-ATC mixture under conditions that promote hybridization between the amplification target circle and the rolling circle replication primer in the primer-ATC mixture,

wherein the amplification target circle comprises a single-stranded, circular DNA molecule comprising a primer complement portion, wherein the primer complement portion is complementary to the rolling circle replication primer, and

(c) mixing DNA polymerase with the primer-ATC mixture, to produce a polymerase-ATC mixture, and incubating the polymerase-ATC mixture under conditions that promote replication of the amplification target circle,

wherein replication of the amplification target circle results in the formation of tandem sequence DNA.

56. A method for detecting nucleic acid molecules, the method comprising

a DNA ligation operation and an amplification operation,

wherein the DNA ligation operation comprises circularization of an open circle probe, wherein circularization of the open circle probe is dependent on hybridization of the open circle probe to a target sequence, wherein the target sequence is coupled to a specific binding molecule, wherein the specific binding molecule can interact with a target molecule, wherein the target molecule is a nucleic acid molecule,

wherein the amplification operation comprises rolling circle replication of the circularized open circle probe to produce tandem sequence DNA.

57. The method of claim 56 wherein the specific binding molecule is bound to a target molecule.

58. The method of claim 56 wherein the method includes a step of bringing the specific binding molecule into contact with the target molecule.

59. The method of claim 56 wherein the amplification operation produces tandem sequence DNA and secondary tandem sequence DNA, wherein the method further comprises detecting the tandem sequence DNA, the secondary tandem sequence DNA, or both.

60. The method of claim 56 wherein a plurality of different target sequences are used in the amplification operation.

61. The method of claim 60 wherein the rolling circle replication primers are each coupled to a different specific binding molecule.

62. The method of claim 61 wherein the different specific binding molecules each interacts with a different target molecule.

63. A method of detecting nucleic acid molecules, the method comprising,

(a) mixing a specific binding molecule with a target sample comprising a target molecule wherein a target sequence is coupled to the specific binding molecule, wherein the specific binding molecule binds to the target molecule,

wherein the target molecule is a nucleic acid molecule,

(b) mixing an open circle probe with the target sample, to produce an OCP-target sample mixture, and incubating the OCP-target sample mixture under conditions that promote hybridization between the open circle probe and the target sequence in the OCP-target sample mixture,

(c) mixing ligase with the OCP-target sample mixture, to produce a ligation mixture, and incubating the ligation mixture under conditions that promote ligation of the open circle probe to form an amplification target circle,

(d) mixing a rolling circle replication primer with the ligation mixture, to produce a primer-ATC mixture, and incubating the primer-ATC mixture under conditions that promote hybridization between the amplification target circle and the rolling circle replication primer in the primer-ATC mixture, and

(e) mixing DNA polymerase with the primer-ATC mixture, to produce a polymerase-ATC mixture, and incubating the polymerase-ATC mixture under conditions that promote replication of the amplification target circle,

wherein replication of the amplification target circle results in the formation of tandem sequence DNA.

64. A method comprising

an amplification operation,

wherein a nucleic acid tag is coupled to a specific binding molecule, wherein the specific binding molecule can interact with a target molecule, wherein the target molecule is a nucleic acid molecule,

wherein the amplification operation comprises rolling circle replication of an amplification target circle to produce tandem sequence DNA.

65. The method of claim 64 wherein the specific binding molecule is bound to a target molecule.

66. The method of claim 64 further comprising bringing the specific binding molecule into contact with the target molecule.

67. The method of claim 64 wherein the method includes a step of bringing the specific binding molecule into contact with the target molecule.

68. A method of detecting target molecules, the method comprising,

(a) mixing a rolling circle replication primer with an amplification target circle, to produce a primer-ATC mixture, and incubating the primer-ATC mixture under conditions that promote hybridization between the amplification target circle and the rolling circle replication primer in the primer-ATC mixture,

wherein the amplification target circle comprises a single-stranded, circular DNA molecule comprising a primer complement portion, wherein the primer complement portion is complementary to the rolling circle replication primer,

wherein the rolling circle replication primer is coupled to a specific binding molecule, and

(b) mixing DNA polymerase with the primer-ATC mixture, to produce a polymerase-ATC mixture, and incubating the polymerase-ATC mixture under conditions that promote replication of the amplification target circle,

wherein replication of the amplification target circle results in the formation of tandem sequence DNA,

(c) mixing the specific binding molecule with a target sample comprising a target molecule, wherein the specific binding molecule binds to the target molecule.

69. The method of claim 68 wherein the target molecule is a nucleic acid molecule, wherein the specific binding molecule is an oligonucleotide complementary to a nucleotide sequence in the nucleic acid molecule.

70. The method of claim 68 wherein the target molecule is a protein.