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Cited by 850

The DOI matches its Crossref record; 25 of the 25 references it cites were found in a registry or an index.

The antiviral compound remdesivir potently inhibits RNA-dependent RNA polymerase from Middle East respiratory syndrome coronavirus

Open access
Gordon, Calvin J., Tchesnokov, Egor P., Feng, Joy Y., Porter, Danielle P., Götte, Matthias·2020·Journal of Biological Chemistry

Abstract

Antiviral drugs for managing infections with human coronaviruses are not yet approved, posing a serious challenge to current global efforts aimed at containing the outbreak of severe acute respiratory syndrome–coronavirus 2 (CoV-2). Remdesivir (RDV) is an investigational compound with a broad spectrum of antiviral activities against RNA viruses, including severe acute respiratory syndrome–CoV and Middle East respiratory syndrome (MERS–CoV). RDV is a nucleotide analog inhibitor of RNA-dependent RNA polymerases (RdRps). Here, we co-expressed the MERS–CoV nonstructural proteins nsp5, nsp7, nsp8, and nsp12 (RdRp) in insect cells as a part a polyprotein to study the mechanism of inhibition of MERS–CoV RdRp by RDV. We initially demonstrated that nsp8 and nsp12 form an active complex. The triphosphate form of the inhibitor (RDV-TP) competes with its natural counterpart ATP. Of note, the selectivity value for RDV-TP obtained here with a steady-state approach suggests that it is more efficiently incorporated than ATP and two other nucleotide analogs. Once incorporated at position i , the inhibitor caused RNA synthesis arrest at position i + 3. Hence, the likely mechanism of action is delayed RNA chain termination. The additional three nucleotides may protect the inhibitor from excision by the viral 3′–5′ exonuclease activity. Together, these results help to explain the high potency of RDV against RNA viruses in cell-based assays.

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Research works printed but not linked: 1

  1. Tchesnokov, 2008, Delayed chain termination protects the anti-hepatitis B virus drug entecavir from excision by HIV-1 reverse transcriptase, J. Biol. Chem, 283, 34218, 10.1074/jbc.M806797200 · doi:10.1074/jbc.m806797200

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Metadata

Authors
Gordon, C. J., Tchesnokov, E. P., Feng, J. Y., Porter, D. P., & Götte, M.
Venue
Journal of Biological Chemistry
Publisher
Elsevier BV
Published
2020-04
Volume
295
Issue
15
Pages
4773-4779
ISSN
0021-9258 (ISSN-L)
OpenAlex
W3007969569
Cited by
850
References
25
FWCI
23.27
Type
journal article
Language
en
Open access
hybrid
Licence
Funders
  • Gouvernement du Canada | Canadian Institutes of Health Research (159507)
  • Alberta Ministry of Economic Development, Trade, and Tourism by the Major Innovation Fund Program (AMR-One Health Consortium)

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CoChat. (2026). Citation check: The antiviral compound remdesivir potently inhibits RNA-dependent RNA polymerase from Middle East respiratory syndrome coronavirus. https://app.cochat.ai/papers/10.1074/jbc.ac120.013056
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Gordon, C. J., Tchesnokov, E. P., Feng, J. Y., Porter, D. P., & Götte, M. (2020). The antiviral compound remdesivir potently inhibits RNA-dependent RNA polymerase from Middle East respiratory syndrome coronavirus. Journal of Biological Chemistry. https://doi.org/10.1074/jbc.ac120.013056

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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