CasZ compositions and methods of use
Provided are compositions and methods that include one or more of: (1) a “CasZ” protein (also referred to as a CasZ polypeptide), a nucleic acid encoding the CasZ protein, and/or a modified host cell comprising the CasZ protein (and/or a nucleic acid encoding the same); (2) a CasZ guide RNA that binds to and provides sequence specificity to the CasZ protein, a nucleic acid encoding the CasZ guide RNA, and/or a modified host cell comprising the CasZ guide RNA (and/or a nucleic acid encoding the same); and (3) a CasZ transactivating noncoding RNA (trancRNA) (referred to herein as a “CasZ trancRNA”), a nucleic acid encoding the CasZ trancRNA, and/or a modified host cell comprising the CasZ trancRNA (and/or a nucleic acid encoding the same).
1. A method of detecting target nucleic acids in a sample comprising a first target nucleic acid and a second target nucleic acid, the method comprising:
A) contacting the sample to:
1 ) one or more detector nucleic acids; and
2 ) a composition comprising:
a) a polypeptide comprising an amino acid sequence that is at least 95% identical to the amino acid sequence of SEQ ID NO: 3;
b) a first guide nucleic acid comprising: i) a first region that binds to the polypeptide; and
ii) a first guide sequence that hybridizes to a first segment of the first target nucleic acid, and
c) a second guide nucleic acid comprising: i) a second region that binds to the polypeptide; and ii) a second guide sequence that hybridizes to a second segment of the second target nucleic acid; and
B) assaying for a signal produced by cleavage of the one or more detector nucleic acids by the polypeptide.
2. The method of claim 1 , further comprising contacting the sample to one or more additional guide nucleic acids that hybridize to a segment of one or more additional target nucleic acids.
3. The method of claim 1 , wherein the first target nucleic acid, the second target nucleic acid, or a combination thereof is single stranded.
4. The method of claim 1 , wherein the first target nucleic acid, the second target nucleic acid, or a combination thereof is double stranded.
5. The method of claim 1 , wherein the first target nucleic acid, the second target nucleic acid, or a combination thereof is present in the sample at a concentration of 100 fM or less.
6. The method of claim 1 , wherein the first target nucleic acid, the second target nucleic acid, or any combination thereof is present in the sample at a ratio of less than one copy per 10 7 non-target nucleic acids.
7. The method of claim 1 , wherein the first target nucleic acid, the second target nucleic acid, or a combination thereof comprises a bacterial nucleic acid, an amplified bacterial nucleic acid, or a combination thereof.
8. The method of claim 1 , wherein the first target nucleic acid, the second target nucleic acid, or a combination thereof comprises a viral nucleic acid, an amplified viral nucleic acid, or a combination thereof.
9. The method of claim 8 , wherein the viral nucleic acid is from a virus selected from the group consisting of: papovavirus, human papillomavirus (HPV), hepadnavirus, Hepatitis B Virus (HBV), herpesvirus, varicella zoster virus (VZV), Epstein Barr virus (EBV), Kaposi's sarcoma-associated herpesvirus, adenovirus, poxvirus, parvovirus, influenza virus, and respiratory syncytial virus nucleic acid.
10. The method of claim 1 , wherein the first target nucleic acid, the second target nucleic acid, or both comprises a eukaryotic nucleic acid, an amplified eukaryotic nucleic acid, or a combination thereof.
11. The method of claim 1 , wherein the first target nucleic acid, the second target nucleic acid, or both comprise a single nucleotide polymorphism.
12. The method of claim 1 , wherein the sample comprises a cancer cell or a cancer cell lysate.
13. The method of claim 1 , wherein the first target nucleic acid and the second target nucleic acid are different.
14. The method of claim 1 , wherein the first target nucleic acid and the second target nucleic acid are the same.
15. The method of claim 1 , wherein the length of the polypeptide is 400 to 800 linked amino acids.
16. The method of claim 1 , wherein the one or more detector nucleic acids comprises at least one component of a fluorescence-emitting dye pair that produces the signal.
17. The method of claim 16 , wherein the fluorescence-emitting dye pair is a fluorophore and a quencher pair or a fluorophore pair.
18. The method of claim 1 , wherein the assaying comprises detecting a change in the signal, and wherein the change is selected from the group consisting of a decrease in an intensity of the signal, an increase in the intensity of the signal, and a change in a wavelength of the signal.
19. The method of claim 1 , wherein the one or more detector nucleic acids comprises single stranded DNA.
20. The method of claim 1 , wherein the assaying comprises:
(i) measuring the signal to generate a test measurement;
(ii) measuring a signal produced by a reference sample to generate a reference measurement; and
(iii) comparing the test measurement to the reference measurement to determine an amount of the first target nucleic acid, the second nucleic acid, or a combination thereof.
21. The method of claim 1 , wherein the polypeptide comprises an amino acid sequence that is at least 98% identical to the amino acid sequence of SEQ ID NO:3.
22. The method of claim 1 , wherein the first region and the second region are the same.
23. The method of claim 1 , wherein the amino acid sequence of the polypeptide is at least 99% identical to the amino acid sequence of SEQ ID NO: 3.
24. The method of claim 1 , wherein the target nucleic acid is a eukaryotic nucleic acid.
25. The method of claim 1 , wherein the first guide nucleic acid or the second guide nucleic acid comprises a heterologous sequence.
26. The method of claim 1 , wherein the polypeptide cleaves one or more of the one or more detector nucleic acids in a non-sequence specific manner upon activation of the polypeptide.
27. The method of claim 1 , wherein the method comprises assaying for a signal produced by cleavage of the one or more detector nucleic acids by the polypeptide upon binding of the polypeptide to the first target nucleic acid, the second target nucleic acid, or a combination thereof.