Discovery of SARS-CoV-2 Papain-like Protease Inhibitors through a Combination of High-Throughput Screening and a FlipGFP-Based Reporter Assay

Ma, Chunlong; Sacco, Michael Dominic; Xia, Zilei; Lambrinidis, George; Townsend, Julia Alma; Hu, Yanmei; Meng, Xiangzhi; Szeto, Tommy; Ba, Mandy; Zhang, Xiujun; Gongora, Maura; Zhang, Fushun; Marty, Michael Thomas; Xiang, Yan; Kolocouris, Antonios; Chen, Yu; Wang, Jun

[Image: see text] The papain-like protease (PL(pro)) of SARS-CoV-2 is a validated antiviral drug target. Through a fluorescence resonance energy transfer-based high-throughput screening and subsequent lead optimization, we identified several PL(pro) inhibitors including Jun9-72-2 and Jun9-75-4 with improved enzymatic inhibition and antiviral activity compared to GRL0617, which was reported as a SARS-CoV PL(pro) inhibitor. Significantly, we developed a cell-based FlipGFP assay that can be applied to predict the cellular antiviral activity of PL(pro) inhibitors in the BSL-2 setting. X-ray crystal structure of PL(pro) in complex with GRL0617 showed that binding of GRL0617 to SARS-CoV-2 induced a conformational change in the BL2 loop to a more closed conformation. Molecular dynamics simulations showed that Jun9-72-2 and Jun9-75-4 engaged in more extensive interactions than GRL0617. Overall, the PL(pro) inhibitors identified in this study represent promising candidates for further development as SARS-CoV-2 antivirals, and the FlipGFP-PL(pro) assay is a suitable surrogate for screening PL(pro) inhibitors in the BSL-2 setting.