EMD-6854

Single-particle
4.7 Å
EMD-6854 Deposition: 29/11/2017
Map released: 21/03/2018
Last modified: 23/10/2024
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links

EMD-6854

Structure of JEV-2F2 Fab complex

EMD-6854

Single-particle
4.7 Å
EMD-6854 Deposition: 29/11/2017
Map released: 21/03/2018
Last modified: 23/10/2024
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links
Sample Organism: Japanese encephalitis virus, Mus musculus
Sample: Complex of JEV with 2F2 Fab
Fitted models: 5ywo (Avg. Q-score: -0.014)

Deposition Authors: Qiu X, Lei Y
Structural basis for neutralization of Japanese encephalitis virus by two potent therapeutic antibodies
Qiu X, Lei Y, Yang P , Gao Q, Wang N, Cao L , Yuan S , Huang X, Deng Y, Ma W, Ding T, Zhang F , Wu X , Hu J, Liu SL, Qin C , Wang X , Xu Z , Rao Z
(2018) Nat Microbiol , 3 , 287 - 294
PUBMED: 29379207
DOI: doi:10.1038/s41564-017-0099-x
ISSN: 2058-5276
Abstract:
Japanese encephalitis virus (JEV), closely related to dengue, Zika, yellow fever and West Nile viruses, remains neglected and not well characterized 1 . JEV is the leading causative agent of encephalitis, and is responsible for thousands of deaths each year in Asia. Humoral immunity is essential for protecting against flavivirus infections and passive immunization has been demonstrated to be effective in curing disease2,3. Here, we demonstrate that JEV-specific monoclonal antibodies, 2F2 and 2H4, block attachment of the virus to its receptor and also prevent fusion of the virus. Neutralization of JEV by these antibodies is exceptionally potent and confers clear therapeutic benefit in mouse models. A single 20 μg dose of these antibodies resulted in 100% survival and complete clearance of JEV from the brains of mice. The 4.7 Å and 4.6 Å resolution cryo-electron microscopy structures of JEV-2F2-Fab and JEV-2H4-Fab complexes, together with the crystal structure of 2H4 Fab and our recent near-atomic structure of JEV 4 , unveil the nature and location of epitopes targeted by the antibodies. Both 2F2 and 2H4 Fabs bind quaternary epitopes that span across three adjacent envelope proteins. Our results provide a structural and molecular basis for the application of 2F2 and 2H4 to treat JEV infection.