Center and Network for Targeted Oncology, Muehlackerweg 8, D-69239 Heidelberg, Germany.
Integrative Cancer Consulting, Aptos, CA, United States.
Curr Top Med Chem. 2020;20(16):1423-1433. doi: 10.2174/1568026620999200517043137.
Like other human pathogenic viruses, coronavirus SARS-CoV-2 employs sophisticated macromolecular machines for viral host cell entry, genome replication and protein processing. Such machinery encompasses SARS-CoV-2 envelope spike (S) glycoprotein required for host cell entry by binding to the ACE2 receptor, viral RNA-dependent RNA polymerase (RdRp) and 3-chymotrypsin-like main protease (3Clpro/Mpro). Under the pressure of the accelerating COVID-19 pandemic caused by the outbreak of SARS-CoV-2 in Wuhan, China in December 2019, novel and repurposed drugs were recently designed and identified for targeting the SARS-CoV-2 reproduction machinery, with the aim to limit the spread of SARS-CoV-2 and morbidity and mortality due to the COVID-19 pandemic.
与其他人类致病病毒一样,冠状病毒 SARS-CoV-2 利用复杂的大分子机器进行病毒宿主细胞进入、基因组复制和蛋白加工。这些机器包括 SARS-CoV-2 包膜刺突(S)糖蛋白,该蛋白通过与 ACE2 受体结合而进入宿主细胞,病毒 RNA 依赖性 RNA 聚合酶(RdRp)和 3-糜蛋白酶样主蛋白酶(3Clpro/Mpro)。在中国武汉 2019 年爆发 SARS-CoV-2 导致 COVID-19 大流行的压力下,最近设计并鉴定了新型和重新利用的药物,用于针对 SARS-CoV-2 复制机制,以限制 SARS-CoV-2 的传播以及 COVID-19 大流行导致的发病率和死亡率。