tetano
Editor, Senior Moderator
Science
. 2021 Jun 3;eabi5224.
doi: 10.1126/science.abi5224. Online ahead of print.
Fe-S cofactors in the SARS-CoV-2 RNA-dependent RNA polymerase are potential antiviral targets
Nunziata Maio[SUP] 1 [/SUP], Bernard A P Lafont[SUP] 2 [/SUP], Debangsu Sil[SUP] 3 [/SUP], Yan Li[SUP] 4 [/SUP], J Martin Bollinger Jr[SUP] 3 5 [/SUP], Carsten Krebs[SUP] 3 5 [/SUP], Theodore C Pierson[SUP] 6 [/SUP], W Marston Linehan[SUP] 7 [/SUP], Tracey A Rouault[SUP] 8 [/SUP]
Affiliations
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causal agent of coronavirus disease 2019 (COVID-19), uses an RNA-dependent RNA polymerase (RdRp) for the replication of its genome and the transcription of its genes. We found that the catalytic subunit of the RdRp, nsp12, ligates two iron-sulfur metal cofactors in sites that were modeled as zinc centers in the available cryo-electron microscopy structures of the RdRp complex. These metal binding sites are essential for replication and for interaction with the viral helicase. Oxidation of the clusters by the stable nitroxide TEMPOL caused their disassembly, potently inhibited the RdRp, and blocked SARS-CoV-2 replication in cell culture. These iron-sulfur clusters thus serve as cofactors for the SARS-CoV-2 RdRp and are targets for therapy of COVID-19.
. 2021 Jun 3;eabi5224.
doi: 10.1126/science.abi5224. Online ahead of print.
Fe-S cofactors in the SARS-CoV-2 RNA-dependent RNA polymerase are potential antiviral targets
Nunziata Maio[SUP] 1 [/SUP], Bernard A P Lafont[SUP] 2 [/SUP], Debangsu Sil[SUP] 3 [/SUP], Yan Li[SUP] 4 [/SUP], J Martin Bollinger Jr[SUP] 3 5 [/SUP], Carsten Krebs[SUP] 3 5 [/SUP], Theodore C Pierson[SUP] 6 [/SUP], W Marston Linehan[SUP] 7 [/SUP], Tracey A Rouault[SUP] 8 [/SUP]
Affiliations
- PMID: 34083449
- DOI: 10.1126/science.abi5224
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causal agent of coronavirus disease 2019 (COVID-19), uses an RNA-dependent RNA polymerase (RdRp) for the replication of its genome and the transcription of its genes. We found that the catalytic subunit of the RdRp, nsp12, ligates two iron-sulfur metal cofactors in sites that were modeled as zinc centers in the available cryo-electron microscopy structures of the RdRp complex. These metal binding sites are essential for replication and for interaction with the viral helicase. Oxidation of the clusters by the stable nitroxide TEMPOL caused their disassembly, potently inhibited the RdRp, and blocked SARS-CoV-2 replication in cell culture. These iron-sulfur clusters thus serve as cofactors for the SARS-CoV-2 RdRp and are targets for therapy of COVID-19.