๐ Crystal structure of the receptor binding domain of the spike glycoprotein of human betacoronavirus HKU1
ยฉ The Author(s) 2017. Human coronavirus (CoV) HKU1 is a pathogen causing acute respiratory illnesses and so far little is known about its biology. HKU1 virus uses its S1 subunit C-terminal domain (CTD) and not the N-terminal domain like other lineage A ฮฒ-Co. Vs to bind to its yet unknown human receptor. Here we present the crystal structure of HKU1 CTD at 1.9 ร
resolution. The structure consists of three subdomains: core, insertion and subdomain-1 (SD-1). While the structure of the core and SD-1 subdomains of HKU1 are highly similar to those of other ฮฒ-Co. Vs, the insertion subdomain adopts a novel fold, which is largely invisible in the cryo-EM structure of the HKU1 S trimer. We identify five residues in the insertion subdomain that are critical for binding of neutralizing antibodies and two residues essential for receptor binding. Our study contributes to a better understanding of entry, immunity and evolution of CoV S proteins.
keywords
๐ neutralizing antibodies (122)
๐ receptor binding (86)
๐ acute respiratory (1734)
๐ crystal structure (114)
author
๐ค Ou, Xiuyuan
๐ค Guan, Hongxin
๐ค Qin, Bo
๐ค Mu, Zhixia
๐ค Wojdyla, Justyna A.
๐ค Wang, Meitian
๐ค Dominguez, Samuel R.
๐ค Qian, Zhaohui
๐ค Cui, Sheng
year
โฐ 2017
journal
๐ Nature Communications
issn
๐ 20411723
volume
8
number
page
citedbycount
6
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