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ASFV 蛋白的结构与功能多样性。

Structures and Functional Diversities of ASFV Proteins.

机构信息

State Key Laboratory of Agrobiotechnology and Beijing Advanced Innovation Center for Food Nutrition and Human Health, College of Biological Sciences, China Agricultural University, Beijing 100193, China.

出版信息

Viruses. 2021 Oct 21;13(11):2124. doi: 10.3390/v13112124.

Abstract

African swine fever virus (ASFV), the causative pathogen of the recent ASF epidemic, is a highly contagious double-stranded DNA virus. Its genome is in the range of 170~193 kbp and encodes 68 structural proteins and over 100 non-structural proteins. Its high pathogenicity strains cause nearly 100% mortality in swine. Consisting of four layers of protein shells and an inner genome, its structure is obviously more complicated than many other viruses, and its multi-layered structures play different kinds of roles in ASFV replication and survival. Each layer possesses many proteins, but very few of the proteins have been investigated at a structural level. Here, we concluded all the ASFV proteins whose structures were unveiled, and explained their functions from the view of structures. Those structures include ASFV AP endonuclease, dUTPases (E165R), pS273R protease, core shell proteins p15 and p35, non-structural proteins pA151R, pNP868R (RNA guanylyltransferase), major capsid protein p72 (gene ), Bcl-2-like protein A179L, histone-like protein pA104R, sulfhydryl oxidase pB119L, polymerase X and ligase. These novel structural features, diverse functions, and complex molecular mechanisms promote ASFV to escape the host immune system easily and make this large virus difficult to control.

摘要

非洲猪瘟病毒(ASFV)是导致近期 ASF 疫情的病原体,是一种高度传染性的双链 DNA 病毒。它的基因组大小在 170~193 kbp 之间,编码 68 种结构蛋白和 100 多种非结构蛋白。其高致病性株可导致猪近 100%的死亡率。由四层蛋白壳和一个内部基因组组成,其结构明显比许多其他病毒复杂,其多层结构在 ASFV 的复制和存活中发挥着不同的作用。每个层都有许多蛋白质,但只有很少的蛋白质在结构水平上进行了研究。在这里,我们总结了所有已揭示结构的 ASFV 蛋白,并从结构的角度解释了它们的功能。这些结构包括 ASFV 的 AP 内切酶、dUTP 酶(E165R)、pS273R 蛋白酶、核心壳蛋白 p15 和 p35、非结构蛋白 pA151R、pNP868R(RNA 鸟苷转移酶)、主要衣壳蛋白 p72(基因)、Bcl-2 样蛋白 A179L、组蛋白样蛋白 pA104R、巯基氧化酶 pB119L、聚合酶 X 和连接酶。这些新的结构特征、多样的功能和复杂的分子机制使 ASFV 能够轻易地逃避宿主的免疫系统,使其难以控制。

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