Structural and mechanistic insights into inhibition of the type I-F CRISPR-Cas surveillance complex by AcrIF4

Gao, Z.; Zhang, L.; Ge, Z.; Wang, H.; Yue, Y.; Jiang, Z.; Wang, X.; Xu, C.; Zhang, Y.; Yang, M.; Feng, Y.

doi:10.1101/2022.08.30.504949

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bioRxiv · 10.1101/2022.08.30.504949

Structural and mechanistic insights into inhibition of the type I-F CRISPR-Cas surveillance complex by AcrIF4

Gao, Z.·Zhang, L.·Ge, Z.·Wang, H.·Yue, Y.·Jiang, Z.·Wang, X.·Xu, C.·Zhang, Y.·Yang, M.·Feng, Y.

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Abstract

CRISPR-Cas system provides prokaryotes with protection against mobile genetic elements (MGEs) such as phages. In turn, phages deploy anti-CRISPR (Acr) proteins to evade this immunity. AcrIF4, an Acr targeting the type I-F CRISPR-Cas system, has been reported to bind the crRNA-guided surveillance (Csy) complex. However, it remains controversial whether AcrIF4 inhibits target DNA binding to the Csy complex. Here, we present structural and mechanistic studies into AcrIF4, exploring its unique anti-CRISPR mechanism. While the Csy-AcrIF4 complex displays decreased affinity for target DNA, it is still able to bind the DNA. Structural and functional analyses of the Csy-AcrIF4-dsDNA complex revealed that AcrIF4 binding prevents rotation of the helical bundle (HB) of Cas8f induced by dsDNA binding, therefore resulting in failure of Cas2/3 recruitment and DNA cleavage. Overall, our study provides an interesting example of attack on the nuclease recruitment event by an Acr, but not conventional mechanisms of blocking binding of target DNA.

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Gao, Z., Zhang, L., Ge, Z., Wang, H., Yue, Y., Jiang, Z., Wang, X., Xu, C., Zhang, Y., Yang, M., Feng, Y.. 2022-08-30. Structural and mechanistic insights into inhibition of the type I-F CRISPR-Cas surveillance complex by AcrIF4. https://doi.org/10.1101/2022.08.30.504949

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