Structures of vesicular stomatitis virus glycoprotein G alone and bound to a neutralizing antibody

VSV G mediates viral entry via endocytosis. In the endosome, G undergoes a pH-dependent conformational change from pre- to post-fusion state, catalyzing membrane fusion. No complete structure of G has been reported so far. We present cryo-EM structures of G, isolated from virions using detergent, alone and in complex with the broadly neutralizing antibody 8G5F1 that binds all G conformations. The post-fusion structure reveals a novel rearrangement of the C-terminal part of the G ectodomain, showing that it undergoes a conformational rearrangement and stabilizes the post-fusion trimer by nesting into a groove between adjacent fusion domains. Structures of G-Fab complex show that the epitope belongs to a conserved antigenic site, explaining the broad neutralization capacity of the antibody. This work provides insights into the molecular basis of VSV G mediated fusion and antibody recognition, with potential implications for vaccine development, oncolytic virotherapy.

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Publication Details

Journal
PLoS Pathogens
Published
2025-10-27
DOI
https://doi.org/10.1371/journal.ppat.1013589
Primary Topic
Virus-based gene therapy research
Type
article
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article

Structures of vesicular stomatitis virus glycoprotein G alone and bound to a neutralizing antibody

Yves Gaudin, Malika Ouldali, Marie Minoves, Magali Noiray et al.
PLoS Pathogens
Virus-based gene therapy research
article

Structures of vesicular stomatitis virus glycoprotein G alone and bound to a neutralizing antibody

Yves Gaudin, Malika Ouldali, Marie Minoves, Magali Noiray, Laura Belot, Guy Schoehn, Eleftherios Zarkadas, Aurélie Albertini, Stéphane Roche, Sarah Johari
article en

Abstract

VSV G mediates viral entry via endocytosis. In the endosome, G undergoes a pH-dependent conformational change from pre- to post-fusion state, catalyzing membrane fusion. No complete structure of G has been reported so far. We present cryo-EM structures of G, isolated from virions using detergent, alone and in complex with the broadly neutralizing antibody 8G5F1 that binds all G conformations. The post-fusion structure reveals a novel rearrangement of the C-terminal part of the G ectodomain, showing that it undergoes a conformational rearrangement and stabilizes the post-fusion trimer by nesting into a groove between adjacent fusion domains. Structures of G-Fab complex show that the epitope belongs to a conserved antigenic site, explaining the broad neutralization capacity of the antibody. This work provides insights into the molecular basis of VSV G mediated fusion and antibody recognition, with potential implications for vaccine development, oncolytic virotherapy.

PLoS PathogensVol. 21(10)
Centre National de la Recherche Scientifique (FR), Commissariat à l'Énergie Atomique et aux Énergies Alternatives (FR), Université Paris-Saclay (FR), CEA Grenoble (FR), Institut de Biologie Intégrative de la Cellule (FR), CEA Paris-Saclay (FR), Institut de Biologie Structurale (FR), Université Grenoble Alpes (FR)
Openalex Percentile: Top 67%
Virus-based gene therapy research
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Structures of vesicular stomatitis virus glycoprotein G alone and bound to a neutralizing antibody — Yves Gaudin, Malika Ouldali, et al. · PLoS Pathogens (2025) | TGRS Research Map | TGRS