Endpoint detection of amplified nucleic acids
The present invention relates to probes and primers beneficial for conducting amplification assays, such as those including loop-mediated isothermal amplification reactions. Also described herein are methods for detecting targets using such probes and/or primers.
1. A reaction mixture comprising:
(i) a target nucleic acid comprising a plurality of regions, including a B3 region, a B2 region, a B1 region, a F1c region, a F2c region, and a F3c region from the 5′ to 3′ direction;
(ii) a first amplicon having corresponding regions that are sufficiently complementary to the plurality of regions in the target nucleic acid, wherein the corresponding regions comprise a F3 region, a F2 region, a F1 region, a B1c region, a B2c region, and a B3c region from the 5′ to 3′ direction;
(iii) a duplex comprising:
a forward inner primer comprising a first nucleic acid sequence having sufficient complementarity to the F2c region of the target nucleic acid and further comprising a second nucleic acid sequence having the F1c region; and
a quench probe comprising a third nucleic acid sequence having sufficient complementarity to a first portion of the forward inner primer and further comprising a quencher label operably linked to the third nucleic acid sequence, wherein a melting temperature T m of the quench probe is from 10° C. to 45° C., wherein the T m of the quench probe is at least 5° C. lower than a temperature of an amplification reaction with the reaction mixture, wherein the length of the quench probe is from six to thirteen nucleotides, and wherein the third nucleic acid sequence is a single stranded nucleic acid;
(iv) a backward inner primer comprising a fourth nucleic acid sequence having sufficient complementarity to the B2c region of the first amplicon and further comprising a fifth nucleic acid sequence having the B1c region;
(v) a pair of outer primers comprising:
a forward primer comprising a sixth nucleic acid sequence having the F3 region; and
a backward primer comprising a seventh nucleic acid having the B3 region; and
(vi) a pair of loop primers comprising:
a loop forward primer comprising an eighth nucleic acid having sufficient complementarity to a region between the F1 and F2 regions; and
a loop backward primer comprising a ninth nucleic acid having sufficient complementarity to a region between the B1 and B2 regions.
2. The reaction mixture of claim 1 , further comprising:
a signal probe comprising a tenth nucleic acid sequence having sufficient complementarity to a second portion of the forward inner primer and further comprising a fluorescent label operably linked to the tenth nucleic acid sequence,
wherein the quencher label and the fluorescent label are in proximity to each other when the quench probe and the signal probe are hybridized to the forward inner primer, such that an emission of the fluorescent label is reduced.
3. The reaction mixture of claim 2 , wherein a melting temperature T m of the signal probe is from 20° C. to 50° C.
4. The reaction mixture of claim 3 , wherein the quencher label is operably linked to a 3′-terminus of the quench probe, and wherein the fluorescent label is operably linked to a 5′-terminus of the signal probe.
5. The reaction mixture of claim 3 , wherein the quencher label is operably linked to a 5′-terminus of the quench probe, and wherein the fluorescent label is operably linked to a 3′-terminus of the signal probe.
6. The reaction mixture of claim 3 , wherein the T m is determined under stringent conditions.
7. The reaction mixture of claim 2 , wherein a concentration of the quench probe is in excess of a concentration of the signal probe.
8. The reaction mixture of claim 2 , wherein the length of the signal probe is from six to thirteen nucleotides.
9. The reaction mixture of claim 2 , wherein the signal probe comprises one or more base mismatches, as compared to a nucleic acid sequence that is perfectly complementary to the second portion of the forward inner primer.
10. The reaction mixture of claim 2 , wherein the signal probe comprises one or more modified nucleic acids.
11. The reaction mixture of claim 2 , wherein the signal probe is provided in a dried form, a freeze dried form, and/or a lyophilized form.
12. The reaction mixture of claim 2 , further comprising one or more reagents selected from the group consisting of a divalent cation, a buffer, a nucleotide, a deoxynucleotide, a DNA polymerase, a RNA polymerase, a reverse transcriptase, and an enhancing agent.
13. The reaction mixture of claim 1 , wherein the forward inner primer further comprises a fluorescent label operably linked to the first nucleic acid sequence, and wherein the quencher label and the fluorescent label are in proximity to each other when the quench probe is hybridized to the forward inner primer.
14. The reaction mixture of claim 13 , wherein the quencher label is operably linked to a 3′-terminus of the quench probe, and wherein the fluorescent label is operably linked to a 5′-terminus of the forward inner primer.
15. The reaction mixture of claim 1 , wherein the reaction mixture further comprises a polymerase and/or a reverse transcriptase.
16. The reaction mixture of claim 1 , wherein the quench probe comprises one or more base mismatches, as compared to a nucleic acid sequence that is perfectly complementary to the first portion of the forward inner primer.
17. The reaction mixture of claim 1 , wherein the forward inner primer is configured for a loop-mediated isothermal amplification reaction.
18. The reaction mixture of claim 1 , wherein a concentration of the quench probe is in excess of a concentration of the forward inner primer.
19. The reaction mixture of claim 1 , further comprising a plurality of primers and a plurality of quench probes configured for a multiplexed loop-mediated isothermal amplification reaction.
20. The reaction mixture of claim 1 , wherein the T m of the quench probe is determined under stringent conditions.
21. The reaction mixture of claim 1 , wherein the forward inner primer and/or the quench probe comprises one or more modified nucleic acids.
22. The reaction mixture of claim 1 , wherein the length of the forward inner primer is at least about 30 nucleotides.
23. A reaction mixture comprising:
(i) a target nucleic acid comprising a plurality of regions, including a B3 region, a B2 region, a B1 region, a F1c region, a F2c region, and a F3c region from the 5′ to 3′ direction;
(ii) a first amplicon having corresponding regions that are sufficiently complementary to the plurality of regions in the target nucleic acid, wherein the corresponding regions comprise a F3 region, a F2 region, a F1 region, a B1c region, a B2c region, and a B3c region from the 5′ to 3′ direction;
(iii) a first duplex comprising:
a forward inner primer comprising a first nucleic acid sequence having sufficient complementarity to the F2c region of the first target nucleic acid and further comprising a second nucleic acid sequence having the F1c region;
a first quench probe comprising a third nucleic acid sequence having sufficient complementarity to a first portion of the forward inner primer and further comprising a first quencher label operably linked to the third nucleic acid sequence, wherein a melting temperature T m of the first quench probe is from 10° C. to 45° C., wherein the T m of the first quench probe is at least 5° C. lower than a temperature of an amplification reaction with the reaction mixture, wherein the length of the first quench probe is from six to thirteen nucleotides, and wherein the third nucleic acid sequence is a single stranded nucleic acid;
(iv) a backward inner primer comprising a fourth nucleic acid sequence having sufficient complementarity to the B2c region of the first amplicon and further comprising a fifth nucleic acid sequence having the B1c region;
(v) a pair of outer primers comprising:
a forward primer comprising a sixth nucleic acid sequence having the F3 region; and
a backward primer comprising a seventh nucleic acid having the B3 region; and
(vi) a pair of loop primers comprising:
a loop forward primer comprising an eighth nucleic acid having sufficient complementarity to a region between the F1 and F2 regions; and
a loop backward primer comprising a ninth nucleic acid having sufficient complementarity to a region between the B1 and B2 regions
(vii) a second primer comprising a tenth nucleic acid sequence having sufficient complementarity to a site in a second target nucleic acid; and
(viii) a second quench probe comprising an eleventh nucleic acid sequence having sufficient complementarity to a first portion of the second primer and further comprising a second quencher label operably linked to the eleventh nucleic acid sequence, wherein a melting temperature T m of the second quench probe is from 10° C. to 55° C.
24. The reaction mixture of claim 23 , wherein the forward inner primer further comprises a first fluorescent label operably linked to the first nucleic acid sequence, wherein the second primer further comprises a second fluorescent label operably linked to the tenth nucleic acid sequence, and wherein the first fluorescent label and the second fluorescent label has different excitation and/or emission spectra.
25. The reaction mixture of claim 24 , wherein the first quencher label and the first fluorescent label are in proximity to each other when the first quench probe is hybridized to the forward inner primer, such that an emission of the first fluorescent label is reduced; and wherein the second quencher label and the second fluorescent label are in proximity to each other when the second quench probe is hybridized to the second primer, such that an emission of the second fluorescent label is reduced.
26. The reaction mixture of claim 23 , further comprising:
a first signal probe comprising a twelfth nucleic acid sequence having sufficient complementarity to a second portion of the forward inner primer and further comprising a fluorescent label operably linked to the twelfth nucleic acid sequence; and
a second signal probe comprising a thirteenth nucleic acid sequence having sufficient complementarity to a second portion of the second primer and further comprising a fluorescent label operably linked to the thirteenth nucleic acid sequence,
wherein the first portion of the forward inner primer and the second portion of the forward inner primer are in proximity to each other in the forward inner primer,
wherein the first portion of the second primer and the second portion of the second primer are in proximity to each other in the second primer,
wherein the first quencher label and the first fluorescent label are in proximity to each other when the first quench probe and the first signal probe are hybridized to the forward inner primer, and
wherein the second quencher label and the second fluorescent label are in proximity to each other when the second quench probe and the second signal probe are hybridized to the forward inner primer.
27. The reaction mixture of claim 26 , wherein the length of the first and/or second signal probe is from six to thirteen nucleotides.
28. The reaction mixture of claim 26 , wherein the first signal probe comprises one or more base mismatches, as compared to a nucleic acid sequence that is perfectly complementary to the second portion of the forward inner primer; and/or wherein the second signal probe comprises one or more base mismatches, as compared to a nucleic acid sequence that is perfectly complementary to the second portion of the second primer.
29. The reaction mixture of claim 26 , wherein the first and/or second signal probe comprises one or more modified nucleic acids.
30. The reaction mixture of claim 26 , wherein the first and/or second signal probe is provided in a dried form, a freeze dried form, and/or a lyophilized form.
31. The reaction mixture of claim 26 , further comprising one or more reagents selected from the group consisting of a divalent cation, a buffer, a nucleotide, a deoxynucleotide, a DNA polymerase, a RNA polymerase, a reverse transcriptase, and an enhancing agent.
32. The reaction mixture of claim 23 , further comprising a second duplex that comprises the second quench probe and the second primer, wherein the tenth nucleic acid sequence is a single stranded nucleic acid.
33. The reaction mixture of claim 23 , wherein the length of the second quench probe is from six to thirteen nucleotides.
34. The reaction mixture of claim 23 , wherein the first quench probe comprises one or more base mismatches, as compared to a nucleic acid sequence that is perfectly complementary to the first portion of the forward inner primer; and/or wherein the second quench probe comprises one or more base mismatches, as compared to a nucleic acid sequence that is perfectly complementary to the first portion of the second primer.
35. The reaction mixture of claim 23 , wherein the T m of the first and/or second quench probe is determined under stringent conditions.
36. The reaction mixture of claim 23 , wherein the forward inner primer, the first quench probe, the second primer, and/or the second quench probe comprises one or more modified nucleic acids.
37. The reaction mixture of claim 23 , further comprising one or more reagents selected from the group consisting of a divalent cation, a buffer, a nucleotide, a deoxynucleotide, a DNA polymerase, a RNA polymerase, a reverse transcriptase, and an enhancing agent.
38. The reaction mixture of claim 23 , wherein a concentration of the first quencher probe is in excess of a concentration of the forward inner primer; and/or wherein a concentration of the second quencher probe is in excess of a concentration of the second primer.
39. The reaction mixture of claim 23 , wherein the length of the forward inner primer is at least about 30 nucleotides.