| Literature DB >> 20439109 |
Kurt Swanson1, Xiaolin Wen, George P Leser, Reay G Paterson, Robert A Lamb, Theodore S Jardetzky.
Abstract
The paramyxovirus F protein is a class I viral membrane fusion protein which undergoes a significant refolding transition during virus entry. Previous studies of the Newcastle disease virus, human parainfluenza virus 3 and parainfluenza virus 5 F proteins revealed differences in the pre- and post-fusion structures. The NDV Queensland (Q) F structure lacked structural elements observed in the other two structures, which are key to the refolding and fusogenic activity of F. Here we present the NDV Australia-Victoria (AV) F protein post-fusion structure and provide EM evidence for its folding to a pre-fusion form. The NDV AV F structure contains heptad repeat elements missing in the previous NDV Q F structure, forming a post-fusion six-helix bundle (6HB) similar to the post-fusion hPIV3 F structure. Electrostatic and temperature factor analysis of the F structures points to regions of these proteins that may be functionally important in their membrane fusion activity. Copyright 2010 Elsevier Inc. All rights reserved.Entities:
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Year: 2010 PMID: 20439109 PMCID: PMC2877518 DOI: 10.1016/j.virol.2010.03.050
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616