生物
肽
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
病毒学
2019年冠状病毒病(COVID-19)
冠状病毒
受体
大流行
药品
2019-20冠状病毒爆发
病毒进入
病毒
免疫学
药理学
传染病(医学专业)
疾病
医学
病毒复制
生物化学
内科学
爆发
作者
Zhiyu Liang,Jiamei Wang,Huan Zhang,Gao Li-xia,Jun Xu,Peiran Li,Jie Yang,Xinting Fu,Han Duan,Jiayan Liu,Tiancai Liu,Weifeng Ma,Kun Wu
出处
期刊:Virology
[Elsevier]
日期:2024-06-19
卷期号:597: 110149-110149
标识
DOI:10.1016/j.virol.2024.110149
摘要
Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) poses a significant socioeconomic burden, and combating COVID-19 is imperative. Blocking the SARS-CoV-2 RBD–ACE2 interaction is a promising therapeutic approach for viral infections, as SARS-CoV-2 binds to the ACE2 receptors of host cells via the RBD of spike proteins to infiltrate these cells. We used computer-aided drug design technology and cellular experiments to screen for peptide S4 with high affinity and specificity for the human ACE2 receptor through structural analysis of SARS-CoV-2 and ACE2 interactions. Cellular experiments revealed that peptide S4 effectively inhibited SARS-CoV-2 and HCoV-NL63 viruses from infecting host cells and was safe for cells at effective concentrations. Based on these findings, peptide S4 may be a potential pharmaceutical agent for clinical application in the treatment of the ongoing SARS-CoV-2 pandemic.
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