| Literature DB >> 33483498 |
Daphne Collias1, Chase L Beisel2,3,4.
Abstract
The ever-expanding set of CRISPR technologies and their programmable RNA-guided nucleases exhibit remarkable flexibility in DNA targeting. However, this flexibility comes with an ever-present constraint: the requirement for a protospacer adjacent motif (PAM) flanking each target. While PAMs play an essential role in self/nonself discrimination by CRISPR-Cas immune systems, this constraint has launched a far-reaching expedition for nucleases with relaxed PAM requirements. Here, we review ongoing efforts toward realizing PAM-free nucleases through natural ortholog mining and protein engineering. We also address potential consequences of fully eliminating PAM recognition and instead propose an alternative nuclease repertoire covering all possible PAM sequences.Entities:
Year: 2021 PMID: 33483498 PMCID: PMC7822910 DOI: 10.1038/s41467-020-20633-y
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919