4.8 Article

Engineered anti-CRISPR proteins for optogenetic control of CRISPR-Cas9

Journal

NATURE METHODS
Volume 15, Issue 11, Pages 924-+

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41592-018-0178-9

Keywords

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Funding

  1. Helmholtz association
  2. German Research Council (DFG)
  3. Federal Ministry of Education and Research (BMBF)
  4. German Network for Bioinformatics Infrastructure (HD.HuB as part of de.NBI) [031A537C]
  5. Helmholtz International Graduate School for Cancer Research (DKFZ, Heidelberg)
  6. German Center for Infection Research (DZIF) [TTU-HIV 04.803]
  7. Cystic Fibrosis Foundation Therapeutics (CFFT) [GRIMM15XX0]
  8. Transregional Collaborative Research Center [TRR179]
  9. Cluster of Excellence CellNetworks (DFG) [EXC81]
  10. European Research Council [716058]
  11. Swiss National Science Foundation
  12. Biltema Foundation
  13. CSCS-Swiss National Supercomputing Centre

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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.

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