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Targeting the Main Protease of SARS-CoV-2: From the Establishment of High Throughput Screening to the Design of Tailored Inhibitors.

ABSTRACT: The main protease of SARS-CoV-2 (M^pro ), the causative agent of COVID-19, constitutes a significant drug target. A new fluorogenic substrate was kinetically compared to an internally quenched fluorescent peptide and shown to be ideally suitable for high throughput screening with recombinantly expressed M^pro . Two classes of protease inhibitors, azanitriles and pyridyl esters, were identified, optimized and subjected to in-depth biochemical characterization. Tailored peptides equipped with the unique azanitrile warhead exhibited concomitant inhibition of M^pro and cathepsin L, a protease relevant for viral cell entry. Pyridyl indole esters were analyzed by a positional scanning. Our focused approach towards M^pro inhibitors proved to be superior to virtual screening. With two irreversible inhibitors, azanitrile 8 (k_inac /K_i =37 500 m^-1 s^-1 , K_i =24.0 nm) and pyridyl ester 17 (k_inac /K_i =29 100 m^-1 s^-1 , K_i =10.0 nm), promising drug candidates for further development have been discovered.

SUBMITTER: Breidenbach J

PROVIDER: S-EPMC8014119 | biostudies-literature |

REPOSITORIES: biostudies-literature

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