Assay method for target nucleic acid by signal amplification using probe hybridization and restriction

• US 8,916,349 B2
• Filed: 11/23/2010
• Issued: 12/23/2014
• Est. Priority Date: 11/23/2009
• Status: Active Grant

• Current Assignee: Becton, Dickinson & Co
• Original Assignee: Becton, Dickinson & Co
• Inventors: Nadeau, Jim, Hellyer, Tobin
• Primary Examiner(s): Martinell, James
• Application Number:
  US13/511,269
• Publication Number:
  US 20120322067A1
• Time in Patent Office: 1,491 Days
• Field of Search: None
• US Class Current: 435/6.11
• CPC Class Codes: C12Q 1/6813 Hybridisation assays
• CPC Class Codes: C12Q 1/682 Signal amplification
• CPC Class Codes: C12Q 1/6823 Release of bound markers
• CPC Class Codes: C12Q 2521/301 Endonuclease
• CPC Class Codes: C12Q 2525/131 incorporating a restriction site
• CPC Class Codes: C12Q 2525/161 incorporating target specific and non-target specific sites
• CPC Class Codes: C12Q 2525/301 Hairpin oligonucleotides
• CPC Class Codes: C12Q 2537/125 Sandwich assay format

Abstract

Oligonucleotides for detection of nucleic acid in a sample that provide for an amplified signal by recycling probes and probe fragments.

Claims

1. A method of detecting the presence or absence of a target nucleic acid in a sample, comprising:

a) preparing a sample suspected of containing a target nucleic acid;

b) preparing a reaction mixture comprising the sample, first and second oligonucleotide probes, and a sequence specific endonuclease, wherein the first and second oligonucleotide probes each comprise a first sequence and a second sequence, wherein the first sequences of the first and second oligonucleotide probes are complementary with non-overlapping sequences of the target nucleic acid, and wherein the second sequences of each of the first and second oligonucleotide probes are complementary with each other, thus forming a duplex restriction site recognized by the sequence specific endonuclease, and wherein at least one of the first and second oligonucleotide probes comprises a detectable label positioned at one side of the restriction site, and a quenching moiety positioned at the other side of the restriction site, thus allowing the first sequences of the first and second oligonucleotide probes to selectively hybridize with the non-overlapping sequences of the nucleic acid of the target nucleic acid and the second sequences of the first and second oligonucleotide probes to selectively hybridize with each other and thereby form the duplex restriction site, such that, if the target nucleic acid is present in the sample, the sequence specific endonuclease cleaves the duplex at the restriction site, allowing for detection of the label, and denaturing the remaining portion of the oligonucleotide probes from the nucleic acid of the target organism and from each other.

2. The method of claim 1 wherein the sequence specific endonuclease is an enzyme selected from the group consisting of BsoBI, Hinc II, Ava I, Nci I and Fnu 4H.

3. The method of claim 2 wherein the sequence specific endonuclease is BsoBI.

4. The method of claim 1 wherein the reaction mixture is subjected to thermal cycling to denature the cleaved oligonucleotides from the target nucleic acid.

5. The method of claim 4 wherein the thermal cycling temperatures are selected with reference to a melting curve.

6. The method of claim 4 wherein the reaction mixture is maintained at a hybridization temperature that is greater than:

i) the melting temperature of the first oligonucleotide probe to the target nucleic acid;

ii) the melting temperature of the second oligonucleotide probe to the target nucleic acid; and

iii) the melting temperature of a hybrid formed of the first oligonucleotide probe and the second oligonucleotide probe.

7. The method of claim 1 wherein the detectable label is a fluorophore.

8. The method of claim 7 wherein the fluorophore is a xanthene dye.

9. The method of claim 7 wherein the quencher is a rhodamine dye.

10. The method of claim 1 wherein the reaction mixture further comprises a blocking probe.

11. A method of detecting the presence or absence of a target nucleic acid in a sample, comprising:

a) preparing a sample suspected of containing target nucleic acid;

b) preparing a reaction mixture comprising the sample, first, second, and third oligonucleotide probes, and a sequence specific endonuclease wherein the first and second oligonucleotide probes each comprise a first sequence and a second sequence wherein the first sequences of the first and second oligonucleotide probes are complementary with non-overlapping sequences of the target nucleic acid, and wherein the second sequences of each of the first and second oligonucleotide probes are complementary with each other, thus forming a duplex restriction site and wherein the first and second oligonucleotide probes are non-labeled, and the second oligonucleotide probe further comprises a third sequence, at least a portion of which forms a hairpin with the second sequence of the second oligonucleotide probe that prevents the second oligonucleotide probe from hybridizing with the first oligonucleotide probe when the first and second oligonucleotide probes are not bound to the target nucleic acid, wherein the portion of the third sequence hybridizes with the third oligonucleotide probe to form a duplex restriction site;

wherein the third oligonucleotide probe is a non-target specific oligonucleotide probe that comprises a detectable label positioned at one side of a first sequence that hybridizes with the third sequence of the second oligonucleotide probe to form the duplex restriction site, and a quenching moiety positioned at the other side of the first sequence of the third oligonucleotide probe;

if the target nucleic acid is present in the sample, allowing the first sequences of the first and second oligonucleotide probes to selectively hybridize with the non-overlapping sequences of the target nucleic acid;

thus allowing denaturation of the hairpin loop and hybridization between the second sequences of the first and second oligonucleotide probes, cleavage of the previously formed duplex at the restriction site by the sequence specific endonuclease, and separation of the third sequence from the second oligonucleotide probe, and dissociation of the first and second oligonucleotide probes from the target nucleic acid, and a plurality of cycles of;

i) hybridization of the third sequence of the second oligonucleotide probe with the third oligonucleotide probe, thus forming a chemically modified duplex restriction site, ii) nicking a single strand of the chemically modified duplex restriction site by the sequence specific restriction endonuclease, iii) liberating label from quencher, and iv) dissociation of the third oligonucleotide probe from the third sequence of the second oligonucleotide probe; and

detecting signal generated from the label which indicates the presence of the target nucleic acid in the sample.

12. The method of claim 11 wherein the sequence specific endonuclease is an enzyme selected from the group consisting of BsoBI, Hinc II, Ava I, Nci I and Fnu 4H.

13. The method of claim 11 wherein the sequence specific endonuclease is BsoBI.

14. The method of claim 11 wherein the reaction mixture is subjected to thermal cycling to denature the cleaved oligonucleotides from the target nucleic acid.

15. The method of claim 14 wherein the thermal cycling temperatures are selected with reference to a melting curve.

16. The method of claim 14 wherein the reaction mixture is maintained at a hybridization temperature that is greater than:

i) the melting temperature of the first oligonucleotide probe to the target nucleic acid;

ii) the melting temperature of the second oligonucleotide probe to the target nucleic acid; and

iii) the melting temperature of a hybrid formed of the first oligonucleotide probe and the second oligonucleotide probe.

17. The method of claim 11 wherein the detectable label is a fluorophore.

18. The method of claim 17 wherein the fluorophore is a xanthene dye.

19. The method of claim 17 wherein the quencher is a rhodamine dye.

20. The method of claim 11 wherein the chemically modified restriction site is hemimodified.

21. The method of claim 11 wherein the reaction mixture further comprises a blocking probe.

22. A method of detecting the presence or absence of a target nucleic acid in a sample, comprising:

a) preparing a sample suspected of containing target nucleic acid;

b) preparing a reaction mixture comprising;

i) the sample;

ii) a first oligonucleotide probe having a first sequence and a second sequence, a second oligonucleotide probe having a first sequence and a second sequence, and a third oligonucleotide probe having a first sequence and a second sequence; and

iii) a sequence specific endonuclease, wherein

the first oligonucleotide probe has a first sequence that is complementary with a target nucleic acid sequence and a second sequence that is complementary with the first sequence of the second oligonucleotide probe wherein a first portion of the second sequence is a single stranded chemically modified portion of a restriction site, wherein a portion of the first and second sequences of the first oligonucleotide probe form a secondary structure;

the second oligonucleotide probe is a probe that does not hybridize directly to the target, wherein a portion of the first sequence of the second probe is complementary to the single stranded chemically modified portion of the second sequence of the first probe, and the second sequence of the second oligonucleotide probe is complementary with the first sequence of the third oligonucleotide probe wherein a portion of the second sequence of the second probe is a single stranded chemically modified portion of a restriction site, and the first sequence and the second sequence of the second oligonucleotide probe partially overlap and wherein at least portions of the first sequence and second sequence of the second oligonucleotide probe form a secondary structure;

the third oligonucleotide probe is a probe that does not hybridize directly to the target, wherein the first sequence includes a portion that is complementary to the single stranded chemically modified portion of a restriction site of the second oligonucleotide probe and further comprising a detectable label or quencher moiety positioned thereon and the second sequence forms a hairpin loop with a portion of the first sequence and has a detectable label or quencher moiety positioned thereon such that the quencher moiety blocks signal from the detectable label due to their relative positions on the third oligonucleotide probe;

and, if the target nucleic acid is present in the sample, allowing the target nucleic acid and the first sequence of the first oligonucleotide probe to selectively hybridize to form a first complex, in a plurality of cycles, i) allowing at least a portion of the second sequence of the first oligonucleotide probe and the first sequence of the second oligonucleotide probe to selectively hybridize to form a second complex;

ii) cleaving a single strand portion of the duplex restriction site formed by the hybridization of the portion of the second sequence of the first oligonucleotide probe that forms the chemically modified single strand of the duplex restriction site with the complementary sequence on the second probe thereby separating the second sequence of the second oligonucleotide probe from the non-overlapping portion of the first sequence of the second oligonucleotide probe; and

iii) dissociation of the second oligonucleotide probe from the first complex;

and, in a plurality of cycles, i) allowing the second sequence of the second oligonucleotide probe to selectively hybridize with the first sequence of the third oligonucleotide probe to form a third complex thereby separating label from quencher and liberating signal ii) cleaving a single strand duplex restriction site formed by hybridization of the portion of the second sequence of the second oligonucleotide probe with the complementary sequence on the first sequence of the third oligonucleotide probe, iii) liberating label from quencher; and

iv) dissociation of the second sequence of the second oligonucleotide probe from the third oligonucleotide probe;

and detecting signal generated from the label which indicates the presence of the target nucleic acid in the sample.

23. The method of claim 22 wherein the secondary structure is a hairpin.

24. The method of claim 22 wherein the sequence specific endonuclease is an enzyme selected from the group consisting of BsoBI, Hinc II, Ava I, Nci I and Fnu 4H.

25. The method of claim 24 wherein the sequence specific endonuclease is BsoBI.

26. The method of claim 22 wherein the detectable label is a fluorophore.

27. The method of claim 26 wherein the quencher is a rhodamine dye.

28. The method of claim 22 wherein the fluorophore is a xanthene dye.

29. The method of claim 22 wherein the nucleic acid target sequence is a Human Papillomavirus nucleic acid.

30. The method of claim 29 wherein the Human Papillomavirus nucleic acid selected from the group consisting of Human Papillomavirus Type 16 and Human Papillomavirus Type 58.

31. The method of claim 30 wherein the target nucleic acid is selected from the Group consisting of SEQ ID NO. 2 and SEQ ID NO. 3.

32. The method of claim 22 wherein the first oligonucleotide probe is SEQ ID NO. 1, the second oligonucleotide probe is SEQ ID NO. 2 and the third oligonucleotide probe is SEQ ID NO. 3.

33. The method of claim 22 wherein the chemically modified restriction site is hemimodified.

34. The method of claim 22 wherein the reaction mixture further comprises a blocking probe.