Real time cleavage assay
View Patent ↗A cleavage-based real-time PCR assay method is provided. In general terms, the assay method includes subjecting a reaction mixture comprising a) PCR reagents for amplifying a nucleic acid target, and b) flap cleavage reagents for performing a flap cleavage assay on the amplified nucleic acid target to two sets of thermocycling conditions. No additional reagents are added to the reaction between said first and second sets of cycles and, in each cycle of the second set of cycles, cleavage of a flap probe is measured.
1. A method of sample analysis comprising:
subjecting a reaction mixture comprising reagents for amplifying and detecting a target nucleic acid, comprising:
said target nucleic acid;
a set of PCR primers for amplifying said target nucleic acid, wherein said set of PCR primers consists of a single pair of PCR primers that bind to sites in said target nucleic acid;
a polymerase activity;
a nuclease activity; and
a probe that comprises a 5′ fluorophore;
to the following thermocycling conditions:
a first set of 5-15 cycles of:
i. a first temperature of at least 90° C.;
ii. a second temperature in the range of 60° C. to 75° C.;
iii. a third temperature in the range of 65° C. to 75° C.; followed by:
a second set of 20-50 cycles of:
i. a fourth temperature of at least 90° C.;
ii. a fifth temperature that is at least 10° C. lower than said second temperature; and
iii. a sixth temperature in the range of 65° C. to 75° C.;
wherein no additional reagents are added to said reaction between said first and second sets of cycles and, in each cycle of said second set of cycles, cleavage of said 5′ fluorophore from said probe by said nuclease activity is measured.
2. The method of claim 1 , wherein said method comprises measuring cleavage of said 5′ fluorophore from said probe while said reaction mixture is at said fifth temperature.
3. The method of claim 1 , wherein cleavage of said 5′ fluorophore from said probe is measured by detecting fluorescence of said reaction mixture during each of said 20-50 cycles.
4. The method of claim 1 , wherein said polymerase activity and said nuclease activity are provided by a thermostable polymerase.
5. The method of claim 4 , wherein the thermostable polymerase is Taq polymerase.
6. The method of claim 4 , wherein the thermostable polymerase is selected from Taq, Pfu, Pwo, UlTma and Vent.
7. The method of claim 1 , wherein said fifth temperature is in the range 50° C. to 55° C.
8. The method of claim 1 , wherein said thermocycling conditions comprises a first set of 8-12 cycles.
9. The method of claim 1 , wherein said reaction mixture is of a volume in the range of 5 μl to 50 μl, and each of said first to sixth temperatures is, independently, of a duration in the range of 10 seconds to 3 minutes.
10. The method of claim 1 , wherein said second and third temperatures are the same temperature.
11. The method of claim 1 , wherein said method further comprises graphing the amount of cleavage that occurs at each of said second set of cycles, thereby providing an estimate of the abundance of said nucleic acid target.
12. The method of claim 1 , wherein said cleavage indicates a mutation in said nucleic acid target.