| Literature DB >> 30377362 |
Felix Bubeck1, Mareike D Hoffmann1,2, Zander Harteveld3,4, Sabine Aschenbrenner1,2, Andreas Bietz1, Max C Waldhauer1, Kathleen Börner5,6,7, Julia Fakhiri5,6, Carolin Schmelas5,6, Laura Dietz1, Dirk Grimm5,6,7, Bruno E Correia3,4, Roland Eils8,9,10,11, Dominik Niopek12,13.
Abstract
Anti-CRISPR proteins are powerful tools for CRISPR-Cas9 regulation; the ability to precisely modulate their activity could facilitate spatiotemporally confined genome perturbations and uncover fundamental aspects of CRISPR biology. We engineered optogenetic anti-CRISPR variants comprising hybrids of AcrIIA4, a potent Streptococcus pyogenes Cas9 inhibitor, and the LOV2 photosensor from Avena sativa. Coexpression of these proteins with CRISPR-Cas9 effectors enabled light-mediated genome and epigenome editing, and revealed rapid Cas9 genome targeting in human cells.Entities:
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Year: 2018 PMID: 30377362 DOI: 10.1038/s41592-018-0178-9
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547