NOVEL ENGINEERED AND CHIMERIC NUCLEASES
Disclosed herein are engineered nucleases and nuclease systems, including chimeric nucleases and chimeric nuclease systems. Engineered and chimeric nucleases disclosed herein include nucleic acid guided nucleases. Additionally disclosed herein are methods of generating engineered nucleases and methods of using the same.
1 . A method for generating a library of chimeric nuclease nucleic acid sequences, said method comprising:
a. providing a plurality of at least a first and second nuclease nucleic acid comprising at least two domain sequences;
b. replacing at least one of the two domain sequences of the first nuclease nucleic acid sequence with the corresponding domain sequence of the second nuclease nucleic acid sequence, thereby generating the library of chimeric nuclease nucleic acid sequences.
2 . The method of claim 1 , wherein the first and second nucleic acid sequence comprise at least three domain sequences, and wherein two or more domain sequences of the first nuclease nucleic acid are replaced by the corresponding domain sequences of the second nuclease nucleic acid sequence, thereby generating the library of chimeric nuclease nucleic acid sequences.
3 . The method of claim 1 , wherein replacing comprises PCR amplifying the domain sequences.
4 . The method of claim 3 , wherein replacing further comprises performing an in vitro assembly method.
5 . The method of claim 1 , wherein the chimeric nuclease is a chimeric nucleic acid-guided nuclease.
6 . The method of claim 5 , wherein the chimeric nucleic acid-guided nuclease is capable of targeting a target nucleic acid sequence.
7 . The method of claim 5 , wherein one or more of the domain sequences encodes a globular domain.
8 . The method of claim 5 , wherein one or more domain sequences encodes a modular looped out helical domain capable of mediating DNA binding.
9 . The method of claim 5 , wherein one or more domain sequences encodes a globular domain capable of interacting with a displaced DNA sequence complementary to the target DNA sequence.
10 . The method of claim 1 , wherein at least one nuclease sequence is from a nuclease of the Cpf1 family.
11 . A method for generating a library of chimeric nuclease nucleic acid sequences, said method comprising:
a. providing a plurality of at least three nuclease nucleic acids, the nucleases comprising at least three domain sequences;
b. replacing at least one of the three domain sequences of the first nuclease nucleic acid sequence with the corresponding domain sequence of the second nuclease nucleic acid sequence, and replacing at least one of the other three domain sequences of the first nuclease nucleic acid sequence with the corresponding domain sequence of the third nuclease nucleic acid sequence, thereby generating the library of chimeric nuclease nucleic acid sequences.
12 . The method of claim 11 , wherein replacing comprises PCR amplifying the domain sequences.
13 . The method of claim 12 , wherein replacing further comprises performing an in vitro assembly method.
14 . The method of claim 11 , wherein the chimeric nuclease is a chimeric nucleic acid-guided nuclease.
15 . The method of claim 14 , wherein the chimeric nucleic acid-guided nuclease is capable of targeting a target nucleic acid sequence.
16 . The method of claim 14 , wherein one or more of the domain sequences encodes a globular domain.
17 . The method of claim 14 , wherein one or more domain sequences encodes a modular looped out helical domain capable of mediating DNA binding.
18 . The method of claim 14 , wherein one or more domain sequences encodes a globular domain capable of interacting with a displaced DNA sequence complementary to the target DNA sequence.
19 . The method of claim 11 , wherein at least one nuclease nucleic acid is from the Cpf1 family.
20 . The method of claim 11 , wherein at least two nuclease nucleic acids are from the Cpf1 family.