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病毒被膜蛋白限制 cGAS-DNA 相分离以介导免疫逃避。

Viral tegument proteins restrict cGAS-DNA phase separation to mediate immune evasion.

机构信息

CAS Key Laboratory of Infection and Immunity, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China; National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China.

National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

Mol Cell. 2021 Jul 1;81(13):2823-2837.e9. doi: 10.1016/j.molcel.2021.05.002. Epub 2021 May 19.

Abstract

DNA-induced liquid-liquid phase separation of cyclic GMP-AMP synthase (cGAS) triggers a potent response to detect pathogen infection and promote innate immune signaling. Whether and how pathogens manipulate cGAS-DNA condensation to mediate immune evasion is unknown. We report the identification of a structurally related viral tegument protein family, represented by ORF52 and VP22 from gamma- and alpha-herpesvirinae, respectively, that employs a conserved mechanism to restrict cGAS-DNA phase separation. ORF52/VP22 proteins accumulate into, and effectively disrupt, the pre-formed cGAS-DNA condensation both in vitro and in cells. The inhibition process is dependent on DNA-induced liquid-liquid phase separation of the viral protein rather than a direct interaction with cGAS. Moreover, highly abundant ORF52 proteins carried within viral particles are able to target cGAS-DNA phase separation in early infection stage. Our results define ORF52/VP22-type tegument proteins as a family of inhibitors targeting cGAS-DNA phase separation and demonstrate a mechanism for how viruses overcome innate immunity.

摘要

DNA 诱导的环鸟苷酸-腺苷酸合酶 (cGAS) 液-液相分离触发了一种强大的反应,以检测病原体感染并促进先天免疫信号转导。目前还不清楚病原体是否以及如何操纵 cGAS-DNA 凝聚来介导免疫逃避。我们报告了一种结构相关的病毒被膜蛋白家族的鉴定,该家族由γ和α疱疹病毒亚科的 ORF52 和 VP22 代表,分别采用保守机制来限制 cGAS-DNA 相分离。ORF52/VP22 蛋白在体外和细胞内积累并有效地破坏预先形成的 cGAS-DNA 凝聚。该抑制过程依赖于病毒蛋白的 DNA 诱导液-液相分离,而不是与 cGAS 的直接相互作用。此外,病毒颗粒内大量存在的 ORF52 蛋白能够在早期感染阶段靶向 cGAS-DNA 相分离。我们的结果将 ORF52/VP22 型被膜蛋白定义为一类靶向 cGAS-DNA 相分离的抑制剂,并展示了病毒克服先天免疫的一种机制。

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