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.
Authors
- Ge Yang (ORCID: https://orcid.org/0000-0002-0415-0933)
- Fan Bu (ORCID: https://orcid.org/0000-0002-6965-3072)
- Bin Liu (ORCID: https://orcid.org/0000-0002-6581-780X)
- Dong Wang (ORCID: https://orcid.org/0009-0007-0760-8165)
Institutions
- University of Minnesota (US)
- Hormel (United States) (US)
- University of Minnesota Medical Center (US)
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
Funders
- University of Minnesota