AcrIF9 tethers non-sequence specific dsDNA to the CRISPR RNA-guided surveillance complex.

Hirschi, Marscha; Lu, Wang-Ting; Santiago-Frangos, Andrew; Wilkinson, Royce; Golden, Sarah M; Davidson, Alan R; Lander, Gabriel C; Wiedenheft, Blake · Nat Commun · 2020

basic_science · Level V

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Abstract

Bacteria have evolved sophisticated adaptive immune systems, called CRISPR-Cas, that provide sequence-specific protection against phage infection. In turn, phages have evolved a broad spectrum of anti-CRISPRs that suppress these immune systems. Here we report structures of anti-CRISPR protein IF9 (AcrIF9) in complex with the type I-F CRISPR RNA-guided surveillance complex (Csy). In addition to sterically blocking the hybridization of complementary dsDNA to the CRISPR RNA, our results show that AcrIF9 binding also promotes non-sequence-specific engagement with dsDNA, potentially sequestering the complex from target DNA. These findings highlight the versatility of anti-CRISPR mechanisms utilized by phages to suppress CRISPR-mediated immune systems.

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