tetano
Editor, Senior Moderator
Antiviral Res
. 2022 Mar 9;105279.
doi: 10.1016/j.antiviral.2022.105279. Online ahead of print.
Label-free duplex SAMDI-MS screen reveals novel SARS-CoV-2 3CLpro inhibitors
M D Scholle[SUP] 1 [/SUP], P O'Kane[SUP] 1 [/SUP], S Dib[SUP] 1 [/SUP], Z A Gurard-Levin[SUP] 2 [/SUP]
Affiliations
Abstract
The 3-chymotrypsin-like cysteine protease (3CLpro) of severe acute respiratory syndrome conoravirus 2 (SARS-CoV-2) remains a promising therapeutic target to combat COVID-19. Our group recently described a novel duplexed biochemical assay that combines self-assembled monolayers of alkanethiolates on gold with matrix assisted laser desorption ionization (MALDI) time of flight (TOF) mass spectrometry (MS) to simultaneously measure 3CLpro and human rhinovirus 3C protease activities. This study describes applying the assay for the completion of a high-throughput duplexed screen of 300,000 diverse, drug-like small molecules in 3 days. The hits were confirmed and evaluated in dose response analyses against recombinant 3CLpro, HRV3C, and the human Cathepsin L proteases. The 3CLpro specific inhibitors were further assessed for activity in cellular cytotoxicity and anti-viral assays. Structure activity relationship studies informed on structural features required for activity and selectivity to 3CLpro over HRV3C. These results will guide the optimization of 3CLpro selective inhibitors to combat COVID-19 along with antiviral compounds against coronaviruses and rhinoviruses.
Keywords: COVID-19; Coronavirus; High-throughput screening; Mass spectrometry; Protease inhibitor; Rhinovirus.
. 2022 Mar 9;105279.
doi: 10.1016/j.antiviral.2022.105279. Online ahead of print.
Label-free duplex SAMDI-MS screen reveals novel SARS-CoV-2 3CLpro inhibitors
M D Scholle[SUP] 1 [/SUP], P O'Kane[SUP] 1 [/SUP], S Dib[SUP] 1 [/SUP], Z A Gurard-Levin[SUP] 2 [/SUP]
Affiliations
- PMID: 35278580
- DOI: 10.1016/j.antiviral.2022.105279
Abstract
The 3-chymotrypsin-like cysteine protease (3CLpro) of severe acute respiratory syndrome conoravirus 2 (SARS-CoV-2) remains a promising therapeutic target to combat COVID-19. Our group recently described a novel duplexed biochemical assay that combines self-assembled monolayers of alkanethiolates on gold with matrix assisted laser desorption ionization (MALDI) time of flight (TOF) mass spectrometry (MS) to simultaneously measure 3CLpro and human rhinovirus 3C protease activities. This study describes applying the assay for the completion of a high-throughput duplexed screen of 300,000 diverse, drug-like small molecules in 3 days. The hits were confirmed and evaluated in dose response analyses against recombinant 3CLpro, HRV3C, and the human Cathepsin L proteases. The 3CLpro specific inhibitors were further assessed for activity in cellular cytotoxicity and anti-viral assays. Structure activity relationship studies informed on structural features required for activity and selectivity to 3CLpro over HRV3C. These results will guide the optimization of 3CLpro selective inhibitors to combat COVID-19 along with antiviral compounds against coronaviruses and rhinoviruses.
Keywords: COVID-19; Coronavirus; High-throughput screening; Mass spectrometry; Protease inhibitor; Rhinovirus.