Synthetic chimeric nucleases function for efficient genome editing
CRISPR-Cas systems have well characterized, modular structures. Here the authors use that architecture to design a Cas12a library of 560 synthetic chimeras, with altered PAM preferences and specificities.
Enregistré dans:
Auteurs principaux: | R. M. Liu, L. L. Liang, E. Freed, H. Chang, E. Oh, Z. Y. Liu, A. Garst, C. A. Eckert, R. T. Gill |
---|---|
Format: | article |
Langue: | EN |
Publié: |
Nature Portfolio
2019
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/b3426a5c4a194f89b3f9de6d909729e5 |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
Diversifying the structure of zinc finger nucleases for high-precision genome editing
par: David E. Paschon, et autres
Publié: (2019) -
Enhanced genome editing efficiency of CRISPR PLUS: Cas9 chimeric fusion proteins
par: Jongjin Park, et autres
Publié: (2021) -
Author Correction: Enhanced genome editing efficiency of CRISPR PLUS: Cas9 chimeric fusion proteins
par: Jongjin Park, et autres
Publié: (2021) -
Author Correction: Genome editing in plants using CRISPR type I-D nuclease
par: Keishi Osakabe, et autres
Publié: (2021) -
Multi-reporter selection for the design of active and more specific zinc-finger nucleases for genome editing
par: Benjamin L. Oakes, et autres
Publié: (2016)