Programmable nuclease improvements and compositions and methods for nucleic acid amplification and detection
Disclosed herein are compositions, kits, and methods related to improved Cas activity. Through compositions and kits disclosed herein and practice of methods disclosed herein, one attains improved Cas activity such as Cas12 activity relative to Cas proteins in the art such as LbCas12. Further described herein are methods to detect target nucleic acid using a programmable nuclease system. Often, the target nucleic acids are present in at low frequency in the sample. Provided herein are methods for enriching these target nucleic acids for detection. Also described herein are methods to insert a PAM sequence into a target sequence of interest for use in a detection comprising a programmable nuclease.
1. A composition comprising:
a) a programmable nuclease having a turnover rate of at least 0.1 cleaved detector nucleic acid molecules per minute, and
b) a non-naturally occurring guide nucleic acid capable of hybridizing to a segment of a target nucleic acid,
wherein the programmable nuclease comprises (i) three partial RuvC domains and (ii) an amino acid sequence at least 65% identical to SEQ ID NO: 11,
wherein, if the non-naturally occurring guide nucleic acid hybridizes to the segment of the target nucleic acid, the programmable nuclease is activated to non-specifically cleave a detector nucleic acid, and
wherein, if the turnover rate is quantified, it is quantified by determining the maximum trans cleavage velocity of the composition in a trans-cleavage reaction occurring at a temperature of from 25° C. to 45° C. divided by the amount of the composition in the trans-cleavage reaction.
2. The composition of claim 1 , wherein the programmable nuclease recognizes a protospacer adjacent motif of YYN, wherein the Y is a C nucleotide or a T nucleotide, and wherein the N is any nucleotide.
3. The composition of claim 1 , wherein the programmable nuclease recognizes a protospacer adjacent motif of YR, wherein the Y is a C nucleotide or a T nucleotide and wherein the R is an A nucleotide or a G nucleotide.
4. The composition of claim 1 , wherein the programmable nuclease is a Type V programmable nuclease.
5. The composition of claim 1 , wherein the programmable nuclease is a Cas12 nuclease.
6. The composition of claim 1 , wherein the three partial RuvC domains comprise a RuvC-I subdomain, a RuvC-II subdomain, and a RuvC-III subdomain.
7. The composition of claim 1 , wherein the programmable nuclease exhibits the turnover rate after heating the composition to a temperature of greater than 45° C. and restoring the temperature to from 25° C. to 45° C.
8. The composition of claim 1 , wherein the programmable nuclease exhibits a higher turnover rate than a programmable nuclease having a sequence of SEQ ID NO: 1.
9. The composition of claim 1 , further comprising the detector nucleic acid.
10. The composition of claim 9 , wherein the detector nucleic acid comprises a detection moiety.
11. The composition of claim 10 , wherein the detection moiety comprises a fluorescent moiety, a quenching moiety, or a combination thereof.
12. The composition of claim 9 , wherein the detector nucleic acid comprises DNA, RNA, or a combination thereof.
13. The composition of claim 1 , further comprising the target nucleic acid.
14. The composition of claim 13 , wherein the target nucleic acid comprises a protospacer adjacent motif.
15. The composition of claim 14 , wherein the protospacer adjacent motif is inserted into the target nucleic acid by amplifying the target nucleic acid.
16. The composition of claim 13 , wherein the target nucleic acid comprises DNA.
17. The composition of claim 13 , wherein the target nucleic acid comprises reverse transcribed cDNA.
18. The composition of claim 13 , wherein the target nucleic acid comprises amplified DNA or reverse transcribed and amplified cDNA.
19. The composition of claim 1 , wherein the programmable nuclease cleaves the detector nucleic acid molecules with an efficiency of at least 40%, wherein, if efficiency is measured, it is measured by a change in a signal produced by a population of detector nucleic acid molecules in a reaction performed at a temperature of about from 25° C. to 45° C., wherein the reaction comprises:
at least 100 nM of the programmable nuclease,
at least 125 nM of the guide nucleic acid, and
at least 1 nM of the target nucleic acid.
20. The composition of claim 1 , further comprising a buffer comprising a buffering agent, a salt, a crowding agent, a detergent, or any combination thereof.
21. The composition of claim 20 , wherein the buffer comprises the salt at less than about 110 mM and wherein the buffer has a pH of from 7 to 8.
22. The composition of claim 20 , wherein the buffer comprises the crowding agent or a competitor.
23. The composition of claim 1 , wherein the programmable nuclease has a turnover rate of from 0.1 to 0.5 cleaved detector nucleic acid molecules per minute.
24. The composition of claim 1 , wherein the programmable nuclease comprises an amino acid sequence at least 80% identical to SEQ ID NO: 11.
25. The composition of claim 1 , wherein the programmable nuclease comprises an amino acid sequence at least 95% identical to SEQ ID NO: 11.
26. The composition of claim 1 , wherein the programmable nuclease comprises an amino acid sequence of SEQ ID NO: 11.