J Alsaadi Entedar A, Jones Ian M
Biomedical Sciences, School of Biological Sciences, University of Reading, Reading RG6 6AJ, UK.
Department of Microbiology, College of Medicine, Thiqar University, Thiqar, Iraq.
Future Virol. 2019 Apr;14(4):275-286. doi: 10.2217/fvl-2018-0144. Epub 2019 Apr 29.
Coronaviruses (CoVs) infect many species causing a variety of diseases with a range of severities. Their members include zoonotic viruses with pandemic potential where therapeutic options are currently limited. Despite this diversity CoVs share some common features including the production, in infected cells, of elaborate membrane structures. Membranes represent both an obstacle and aid to CoV replication - and in consequence - virus-encoded structural and nonstructural proteins have membrane-binding properties. The structural proteins encounter cellular membranes at both entry and exit of the virus while the nonstructural proteins reorganize cellular membranes to benefit virus replication. Here, the role of each protein in membrane binding is described to provide a comprehensive picture of their role in the CoV replication cycle.
冠状病毒(CoVs)感染多种物种,引发一系列严重程度各异的疾病。其成员包括具有大流行潜力的人畜共患病毒,目前针对这些病毒的治疗选择有限。尽管存在这种多样性,冠状病毒仍具有一些共同特征,包括在受感染细胞中产生精细的膜结构。膜既是冠状病毒复制的障碍,也是其助力——因此,病毒编码的结构蛋白和非结构蛋白都具有膜结合特性。结构蛋白在病毒的进入和退出过程中都会与细胞膜接触,而非结构蛋白则会重组细胞膜以利于病毒复制。在此,将描述每种蛋白在膜结合中的作用,以全面呈现它们在冠状病毒复制周期中的作用。