Structure of Acidic pH Dengue Virus Showing the Fusogenic Glycoprotein Trimers
Author(s) -
Xinzheng Zhang,
Ju Sheng,
S. Kyle Austin,
Tabitha E. Hoornweg,
Jolanda M. Smit,
Richard Kühn,
Michael S. Diamond,
Michael G. Rossmann
Publication year - 2014
Publication title -
journal of virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.617
H-Index - 292
eISSN - 1070-6321
pISSN - 0022-538X
DOI - 10.1128/jvi.02411-14
Subject(s) - biology , glycoprotein , dengue virus , virology , dengue fever , virus , biochemistry
Flaviviruses undergo large conformational changes during their life cycle. Under acidic pH conditions, the mature virus forms transient fusogenic trimers of E glycoproteins that engage the lipid membrane in host cells to initiate viral fusion and nucleocapsid penetration into the cytoplasm. However, the dynamic nature of the fusogenic trimer has made the determination of its structure a challenge. Here we have used Fab fragments of the neutralizing antibody DV2-E104 to stop the conformational change of dengue virus at an intermediate stage of the fusion process. Using cryo-electron microscopy, we show that in this intermediate stage, the E glycoproteins form 60 trimers that are similar to the predicted "open" fusogenic trimer.
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