冠状病毒
穗蛋白
受体
蛋白质结构
2019年冠状病毒病(COVID-19)
氨基末端
结合位点
生物
血浆蛋白结合
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
病毒学
细胞生物学
生物物理学
化学
肽序列
生物化学
医学
传染病(医学专业)
基因
病理
疾病
作者
Fang Li,Wenhui Li,Michael Farzan,Stephen C. Harrison
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2005-09-15
卷期号:309 (5742): 1864-1868
被引量:2196
标识
DOI:10.1126/science.1116480
摘要
The spike protein (S) of SARS coronavirus (SARS-CoV) attaches the virus to its cellular receptor, angiotensin-converting enzyme 2 (ACE2). A defined receptor-binding domain (RBD) on S mediates this interaction. The crystal structure at 2.9 angstrom resolution of the RBD bound with the peptidase domain of human ACE2 shows that the RBD presents a gently concave surface, which cradles the N-terminal lobe of the peptidase. The atomic details at the interface between the two proteins clarify the importance of residue changes that facilitate efficient cross-species infection and human-to-human transmission. The structure of the RBD suggests ways to make truncated disulfide-stabilized RBD variants for use in the design of coronavirus vaccines.
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