Li Fang
Department of Pharmacology, University of Minnesota Medical School, Minneapolis, Minnesota, USA
J Virol. 2015 Feb;89(4):1954-64. doi: 10.1128/JVI.02615-14. Epub 2014 Nov 26.
Receptor recognition by viruses is the first and essential step of viral infections of host cells. It is an important determinant of viral host range and cross-species infection and a primary target for antiviral intervention. Coronaviruses recognize a variety of host receptors, infect many hosts, and are health threats to humans and animals. The receptor-binding S1 subunit of coronavirus spike proteins contains two distinctive domains, the N-terminal domain (S1-NTD) and the C-terminal domain (S1-CTD), both of which can function as receptor-binding domains (RBDs). S1-NTDs and S1-CTDs from three major coronavirus genera recognize at least four protein receptors and three sugar receptors and demonstrate a complex receptor recognition pattern. For example, highly similar coronavirus S1-CTDs within the same genus can recognize different receptors, whereas very different coronavirus S1-CTDs from different genera can recognize the same receptor. Moreover, coronavirus S1-NTDs can recognize either protein or sugar receptors. Structural studies in the past decade have elucidated many of the puzzles associated with coronavirus-receptor interactions. This article reviews the latest knowledge on the receptor recognition mechanisms of coronaviruses and discusses how coronaviruses have evolved their complex receptor recognition pattern. It also summarizes important principles that govern receptor recognition by viruses in general.
病毒对受体的识别是病毒感染宿主细胞的首要且关键步骤。它是病毒宿主范围和跨物种感染的重要决定因素,也是抗病毒干预的主要靶点。冠状病毒可识别多种宿主受体,感染多种宿主,对人类和动物的健康构成威胁。冠状病毒刺突蛋白的受体结合S1亚基包含两个不同结构域,即N端结构域(S1-NTD)和C端结构域(S1-CTD),二者均可作为受体结合结构域(RBD)发挥作用。来自三个主要冠状病毒属的S1-NTD和S1-CTD至少可识别四种蛋白质受体和三种糖类受体,并呈现出复杂的受体识别模式。例如,同一属内高度相似的冠状病毒S1-CTD可识别不同受体,而来自不同属的差异极大的冠状病毒S1-CTD却可识别相同受体。此外,冠状病毒S1-NTD既可识别蛋白质受体,也可识别糖类受体。过去十年的结构研究揭示了许多与冠状病毒-受体相互作用相关的谜题。本文综述了冠状病毒受体识别机制的最新知识,并探讨了冠状病毒如何演化出其复杂的受体识别模式。文章还总结了病毒受体识别的一般重要原则。