Laboratory of Bacteriology, The Rockefeller University, New York, NY 10065, USA.
Structural Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Science. 2020 Jul 3;369(6499):54-59. doi: 10.1126/science.abb6151. Epub 2020 May 28.
The CRISPR RNA (crRNA)-guided nuclease Cas13 recognizes complementary viral transcripts to trigger the degradation of both host and viral RNA during the type VI CRISPR-Cas antiviral response. However, how viruses can counteract this immunity is not known. We describe a listeriaphage (ϕLS46) encoding an anti-CRISPR protein (AcrVIA1) that inactivates the type VI-A CRISPR system of Using genetics, biochemistry, and structural biology, we found that AcrVIA1 interacts with the guide-exposed face of Cas13a, preventing access to the target RNA and the conformational changes required for nuclease activation. Unlike inhibitors of DNA-cleaving Cas nucleases, which cause limited immunosuppression and require multiple infections to bypass CRISPR defenses, a single dose of AcrVIA1 delivered by an individual virion completely dismantles type VI-A CRISPR-mediated immunity.
CRISPR RNA(crRNA)引导的核酸酶 Cas13 识别互补的病毒转录本,在 VI 型 CRISPR-Cas 抗病毒反应中触发宿主和病毒 RNA 的降解。然而,病毒如何对抗这种免疫尚不清楚。我们描述了一种李斯特菌噬菌体(ϕLS46)编码一种抗 CRISPR 蛋白(AcrVIA1),该蛋白失活了 利用遗传学、生物化学和结构生物学,我们发现 AcrVIA1 与 Cas13a 的暴露在引导物面上相互作用,阻止了对靶 RNA 的访问以及对核酸酶激活所需的构象变化。与限制免疫抑制并需要多次感染来绕过 CRISPR 防御的 DNA 切割 Cas 核酸酶抑制剂不同,单个病毒粒子递送的单次剂量的 AcrVIA1 完全破坏了 VI 型 CRISPR 介导的免疫。