Coupling Cas9 to artificial inhibitory domains enhances CRISPR-Cas9 target specificity

The limited target specificity of CRISPR-Cas nucleases poses a challenge with respect to their application in research and therapy. Here, we present a simple and original strategy to enhance the specificity of CRISPR-Cas9 genome editing by coupling Cas9 to artificial inhibitory domains. Applying a c...

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Main Authors: Aschenbrenner, Sabine (Author) , Kallenberger, Stefan M. (Author) , Hoffmann, Mareike (Author) , Huck, Adrian (Author) , Eils, Roland (Author) , Niopek, Dominik (Author)
Format: Article (Journal)
Language:English
Published: 05 Feb 2020
In: Science advances
Year: 2020, Volume: 6, Issue: 6
ISSN:2375-2548
DOI:10.1126/sciadv.aay0187
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1126/sciadv.aay0187
Verlag, lizenzpflichtig, Volltext: https://advances.sciencemag.org/content/6/6/eaay0187
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Author Notes:Sabine Aschenbrenner, Stefan M. Kallenberger, Mareike D. Hoffmann, Adrian Huck, Roland Eils, Dominik Niopek
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Summary:The limited target specificity of CRISPR-Cas nucleases poses a challenge with respect to their application in research and therapy. Here, we present a simple and original strategy to enhance the specificity of CRISPR-Cas9 genome editing by coupling Cas9 to artificial inhibitory domains. Applying a combination of mathematical modeling and experiments, we first determined how CRISPR-Cas9 activity profiles relate to Cas9 specificity. We then used artificially weakened anti-CRISPR (Acr) proteins either coexpressed with or directly fused to Cas9 to fine-tune its activity toward selected levels, thereby achieving an effective kinetic insulation of ON- and OFF-target editing events. We demonstrate highly specific genome editing in mammalian cells using diverse single-guide RNAs prone to potent OFF-targeting. Last, we show that our strategy is compatible with different modes of delivery, including transient transfection and adeno-associated viral vectors. Together, we provide a highly versatile approach to reduce CRISPR-Cas OFF-target effects via kinetic insulation. - Fusing attenuated anti-CRISPR proteins to Cas9 improves specificity via kinetic insulation of ON- and OFF-target editing events. - Fusing attenuated anti-CRISPR proteins to Cas9 improves specificity via kinetic insulation of ON- and OFF-target editing events.
Item Description:Gesehen am 30.03.2020
Physical Description:Online Resource
ISSN:2375-2548
DOI:10.1126/sciadv.aay0187