Fragment-Based Screen of SARS-CoV-2 Papain-like Protease (PL<sup>pro</sup>)
Ashley J. Taylor, Kangsa Amporndanai, Tyson A. Rietz, Bin Zhao, Anusha Thiruvaipati, Qiangqiang Wei, Taylor M. South, Mackenzie M. Crow, Chideraa Apakama, John Sensintaffar, Jason Phan, Taekyu Lee, Stephen W. Fesik
Abstract
High Resolution Image Download MS PowerPoint Slide 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 Pro ) 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 Pro 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 Pro inhibitors.