脂质双层融合
三聚体
生物
冠状病毒
生物物理学
病毒进入
病毒蛋白
病毒学
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
融合蛋白
细胞生物学
低温电子显微
重组DNA
2019年冠状病毒病(COVID-19)
病毒
化学
基因
生物化学
病毒复制
医学
有机化学
传染病(医学专业)
病理
疾病
二聚体
作者
Yongfei Cai,Jun Zhang,Tianshu Xiao,Hanqin Peng,Sarah M. Sterling,Richard M. Walsh,Shaun Rawson,Sophia Rits‐Volloch,Bing Chen
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2020-09-25
卷期号:369 (6511): 1586-1592
被引量:1037
标识
DOI:10.1126/science.abd4251
摘要
A dynamic viral spike Efforts to protect human cells against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have focused on the trimeric spike (S) protein. Several structures have shown a stabilized ectodomain of the spike in its prefusion conformation. Cai et al. now provide insight into the structural changes in the S protein that result in the fusion of the viral and host cell membranes. They purified full-length S protein and determined cryo–electron microscopy structures of both the prefusion and postfusion conformations. These structures add to our understanding of S protein function and could inform vaccine design. Science , this issue p. 1586
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