tetano
Editor, Senior Moderator
Antiviral Res
. 2022 Jun 15;105364.
doi: 10.1016/j.antiviral.2022.105364. Online ahead of print.
Identification of potent inhibitors of arenavirus and SARS-CoV-2 exoribonucleases by fluorescence polarization assay
Sergio Hernández[SUP] 1 [/SUP], Mikael Feracci[SUP] 1 [/SUP], Carolina Trajano De Jesus[SUP] 1 [/SUP], Priscila El Kazzi[SUP] 1 [/SUP], Rafik Kaci[SUP] 1 [/SUP], Laura Garlatti[SUP] 1 [/SUP], Clemence Mondielli[SUP] 2 [/SUP], Fabrice Bailly[SUP] 3 [/SUP], Philippe Cotelle[SUP] 4 [/SUP], Franck Touret[SUP] 5 [/SUP], Xavier de Lamballerie[SUP] 5 [/SUP], Bruno Coutard[SUP] 5 [/SUP], Etienne Decroly[SUP] 1 [/SUP], Bruno Canard[SUP] 1 [/SUP], François Ferron[SUP] 6 [/SUP], Karine Alvarez[SUP] 7 [/SUP]
Affiliations
Abstract
Viral exoribonucleases are uncommon in the world of RNA viruses. To date, they have only been identified in the Arenaviridae and the Coronaviridae families. The exoribonucleases of these viruses play a crucial role in the pathogenicity and interplay with host innate immune response. Moreover, coronaviruses exoribonuclease is also involved in a proofreading mechanism ensuring the genetic stability of the viral genome. Because of their key roles in virus life cycle, they constitute attractive target for drug design. Here we developed a sensitive, robust and reliable fluorescence polarization assay to measure the exoribonuclease activity and its inhibition in vitro. The effectiveness of the method was validated on three different viral exoribonucleases, including SARS-CoV-2, Lymphocytic Choriomeningitis and Machupo viruses. We performed a screening of a focused library consisting of 113 metal chelators. Hit compounds were recovered with an IC[SUB]50[/SUB] at micromolar level. We confirmed 3 hits in SARS-CoV-2 infected Vero-E6 cells.
Keywords: Arenaviridae; Cellular assays; Coronaviridae; Exoribonuclease activity; Fluorescence polarization; IC(50); Inhibitors; Phosphohydrolase activity; Screening.
. 2022 Jun 15;105364.
doi: 10.1016/j.antiviral.2022.105364. Online ahead of print.
Identification of potent inhibitors of arenavirus and SARS-CoV-2 exoribonucleases by fluorescence polarization assay
Sergio Hernández[SUP] 1 [/SUP], Mikael Feracci[SUP] 1 [/SUP], Carolina Trajano De Jesus[SUP] 1 [/SUP], Priscila El Kazzi[SUP] 1 [/SUP], Rafik Kaci[SUP] 1 [/SUP], Laura Garlatti[SUP] 1 [/SUP], Clemence Mondielli[SUP] 2 [/SUP], Fabrice Bailly[SUP] 3 [/SUP], Philippe Cotelle[SUP] 4 [/SUP], Franck Touret[SUP] 5 [/SUP], Xavier de Lamballerie[SUP] 5 [/SUP], Bruno Coutard[SUP] 5 [/SUP], Etienne Decroly[SUP] 1 [/SUP], Bruno Canard[SUP] 1 [/SUP], François Ferron[SUP] 6 [/SUP], Karine Alvarez[SUP] 7 [/SUP]
Affiliations
- PMID: 35716929
- DOI: 10.1016/j.antiviral.2022.105364
Abstract
Viral exoribonucleases are uncommon in the world of RNA viruses. To date, they have only been identified in the Arenaviridae and the Coronaviridae families. The exoribonucleases of these viruses play a crucial role in the pathogenicity and interplay with host innate immune response. Moreover, coronaviruses exoribonuclease is also involved in a proofreading mechanism ensuring the genetic stability of the viral genome. Because of their key roles in virus life cycle, they constitute attractive target for drug design. Here we developed a sensitive, robust and reliable fluorescence polarization assay to measure the exoribonuclease activity and its inhibition in vitro. The effectiveness of the method was validated on three different viral exoribonucleases, including SARS-CoV-2, Lymphocytic Choriomeningitis and Machupo viruses. We performed a screening of a focused library consisting of 113 metal chelators. Hit compounds were recovered with an IC[SUB]50[/SUB] at micromolar level. We confirmed 3 hits in SARS-CoV-2 infected Vero-E6 cells.
Keywords: Arenaviridae; Cellular assays; Coronaviridae; Exoribonuclease activity; Fluorescence polarization; IC(50); Inhibitors; Phosphohydrolase activity; Screening.