Taylor Ashley J, Amporndanai Kangsa, Rietz Tyson A, Zhao Bin, Thiruvaipati Anusha, Wei Qiangqiang, South Taylor M, Crow Mackenzie M, Apakama Chideraa, Sensintaffar John L, Phan Jason, Lee Taekyu, Fesik Stephen W
Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-0146, United States.
Department of Pharmacology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-6600, United States.
ACS Med Chem Lett. 2024 Jul 23;15(8):1351-1357. doi: 10.1021/acsmedchemlett.4c00238. eCollection 2024 Aug 8.
Coronaviruses have been responsible for numerous viral outbreaks in the past two decades due to the high transmission rate of this family of viruses. The deadliest outbreak is the recent Covid-19 pandemic, which resulted in over 7 million deaths worldwide. SARS-CoV-2 papain-like protease (PL) plays a key role in both viral replication and host immune suppression and is highly conserved across the coronavirus family, making it an ideal drug target. Herein we describe a fragment-based screen against PL using protein-observed NMR experiments, identifying 77 hit fragments. Analyses of NMR perturbation patterns and X-ray cocrystallized structures reveal fragments bind to two distinct regions of the protein. Importantly none of the fragments identified belong to the same chemical class as the few reported inhibitors, allowing for the discovery of a novel class of PL inhibitors.
在过去二十年中,冠状病毒因其高传播率导致了众多病毒爆发。最致命的疫情是最近的新冠疫情,在全球造成了超过700万人死亡。严重急性呼吸综合征冠状病毒2型木瓜样蛋白酶(PL)在病毒复制和宿主免疫抑制中都起着关键作用,并且在冠状病毒家族中高度保守,使其成为理想的药物靶点。在此,我们描述了一项使用蛋白质观测核磁共振实验针对PL的基于片段的筛选,鉴定出77个命中片段。对核磁共振扰动模式和X射线共结晶结构的分析表明,这些片段与该蛋白质的两个不同区域结合。重要的是,所鉴定的片段均不属于少数已报道抑制剂的同一化学类别,从而有可能发现一类新型的PL抑制剂。