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A human antibody against Zika virus crosslinks the E protein to prevent infection

  • S. Saif Hasan
  • , Andrew Miller
  • , Gopal Sapparapu
  • , Estefania Fernandez
  • , Thomas Klose
  • , Feng Long
  • , Andrei Fokine
  • , Jason C. Porta
  • , Wen Jiang
  • , Michael S. Diamond
  • , James E. Crowe
  • , Richard J. Kuhn
  • , Michael G. Rossmann

Research output: Contribution to journalArticlepeer-review

Abstract

The recent Zika virus (ZIKV) epidemic has been linked to unusual and severe clinical manifestations including microcephaly in fetuses of infected pregnant women and Guillian-Barré syndrome in adults. Neutralizing antibodies present a possible therapeutic approach to prevent and control ZIKV infection. Here we present a 6.2 Å resolution three-dimensional cryo-electron microscopy (cryoEM) structure of an infectious ZIKV (strain H/PF/2013, French Polynesia) in complex with the Fab fragment of a highly therapeutic and neutralizing human monoclonal antibody, ZIKV-117. The antibody had been shown to prevent fetal infection and demise in mice. The structure shows that ZIKV-117 Fabs cross-link the monomers within the surface E glycoprotein dimers as well as between neighbouring dimers, thus preventing the reorganization of E protein monomers into fusogenic trimers in the acidic environment of endosomes.

Original languageEnglish (US)
Article number14722
JournalNature communications
Volume8
DOIs
StatePublished - Mar 16 2017

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

All Science Journal Classification (ASJC) codes

  • General Chemistry
  • General Biochemistry, Genetics and Molecular Biology
  • General Physics and Astronomy

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