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ACS Chem Biol ; 17(7): 1937-1950, 2022 07 15.
Artículo en Inglés | MEDLINE | ID: covidwho-2106315

RESUMEN

Inhibition of the protein kinase CSNK2 with any of 30 specific and selective inhibitors representing different chemotypes, blocked replication of pathogenic human, bat, and murine ß-coronaviruses. The potency of in-cell CSNK2A target engagement across the set of inhibitors correlated with antiviral activity and genetic knockdown confirmed the essential role of the CSNK2 holoenzyme in ß-coronavirus replication. Spike protein endocytosis was blocked by CSNK2A inhibition, indicating that antiviral activity was due in part to a suppression of viral entry. CSNK2A inhibition may be a viable target for the development of anti-SARS-like ß-coronavirus drugs.


Asunto(s)
Infecciones por Coronavirus , Coronavirus , Animales , Antivirales/farmacología , Coronavirus/genética , Humanos , Ratones , Internalización del Virus
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