Structure of the Newcastle disease virus F protein in the post-fusion conformation |
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Authors: | Kurt Swanson Xiaolin Wen George P. Leser Robert A. Lamb Theodore S. Jardetzky |
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Affiliation: | a Howard Hughes Medical Institute, USA b Department of Biochemistry, Molecular Biology, and Cell Biology, Northwestern University, Evanston, IL 60208-3500, USA c Department of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305, USA |
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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. |
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Keywords: | Paramyxovirus Membrane fusion Virus entry Class I viral fusion proteins NDV |
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