小核糖核酸科
生物
柯萨奇病毒
肠道病毒
受体
病毒进入
病毒
回声病毒
蛋白质亚单位
病毒学
细胞生物学
病毒复制
遗传学
基因
作者
Xin Zhao,Guigen Zhang,Sheng Liu,Xiangpeng Chen,Ruchao Peng,Lianpan Dai,Xiao Qu,Shihua Li,Hao Song,Zhengrong Gao,Pengfei Yuan,Zhiheng Liu,Changyao Li,Zifang Shang,Yan Li,Meifan Zhang,Jianxun Qi,Han Wang,Ning Du,Yan Wu
出处
期刊:Cell
[Cell Press]
日期:2019-05-01
卷期号:177 (6): 1553-1565.e16
被引量:125
标识
DOI:10.1016/j.cell.2019.04.035
摘要
Enterovirus B (EV-B), a major proportion of the genus Enterovirus in the family Picornaviridae, is the causative agent of severe human infectious diseases. Although cellular receptors for coxsackievirus B in EV-B have been identified, receptors mediating virus entry, especially the uncoating process of echovirus and other EV-B remain obscure. Here, we found that human neonatal Fc receptor (FcRn) is the uncoating receptor for major EV-B. FcRn binds to the virus particles in the “canyon” through its FCGRT subunit. By obtaining multiple cryo-electron microscopy structures at different stages of virus entry at atomic or near-atomic resolution, we deciphered the underlying mechanisms of enterovirus attachment and uncoating. These structures revealed that different from the attachment receptor CD55, binding of FcRn to the virions induces efficient release of “pocket factor” under acidic conditions and initiates the conformational changes in viral particle, providing a structural basis for understanding the mechanisms of enterovirus entry.
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