Structural basis of measles virus polymerase inhibition by nonnucleoside inhibitor ERDRP-0519

ERDRP-0519 is a potent nonnucleoside inhibitor active against measles virus (MeV) and other Morbilliviruses. Here we report cryo-EM structures of the compound bound to MeV polymerase complexes at 2.73 Å and 2.48 Å resolution, revealing a unique binding pocket in the RdRp palm subdomain that overlaps the catalytic GDN motif. These findings clarify the basis of resistance mutations, including W671, and provide a foundation for designing next-generation Paramyxovirus antivirals.

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Publication Details

Journal
Nature Communications
Published
2025-10-13
DOI
https://doi.org/10.1038/s41467-025-64128-0
Primary Topic
Virology and Viral Diseases
Type
article
Field-Weighted Citation Impact
0.00

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article

Structural basis of measles virus polymerase inhibition by nonnucleoside inhibitor ERDRP-0519

Ge Yang, Fan Bu, Bin Liu, Dong Wang
Nature Communications
Virology and Viral Diseases
article

Structural basis of measles virus polymerase inhibition by nonnucleoside inhibitor ERDRP-0519

Ge Yang, Fan Bu, Bin Liu, Dong Wang
article en

Abstract

ERDRP-0519 is a potent nonnucleoside inhibitor active against measles virus (MeV) and other Morbilliviruses. Here we report cryo-EM structures of the compound bound to MeV polymerase complexes at 2.73 Å and 2.48 Å resolution, revealing a unique binding pocket in the RdRp palm subdomain that overlaps the catalytic GDN motif. These findings clarify the basis of resistance mutations, including W671, and provide a foundation for designing next-generation Paramyxovirus antivirals.

Nature CommunicationsVol. 16(1)
University of Minnesota (US), Hormel (United States) (US), University of Minnesota Medical Center (US)
University of Minnesota
Openalex Percentile: Top 61%
Virology and Viral Diseases
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