Abstract
Vesicular stomatitis virus (VSV) is a bullet-shaped rhabdovirus and a model system of negative-strand RNA viruses. Through direct visualization by means of cryo-electron microscopy, we show that each virion contains two nested, left-handed helices: an outer helix of matrix protein M and an inner helix of nucleoprotein N and RNA. M has a hub domain with four contact sites that link to neighboring M and N subunits, providing rigidity by clamping adjacent turns of the nucleocapsid. Side-by-side interactions between neighboring N subunits are critical for the nucleocapsid to form a bullet shape, and structure-based mutagenesis results support this description. Together, our data suggest a mechanism of VSV assembly in which the nucleocapsid spirals from the tip to become the helical trunk, both subsequently framed and rigidified by the M layer.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Cryoelectron Microscopy
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Crystallography, X-Ray
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Image Processing, Computer-Assisted
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Lipid Bilayers
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Models, Molecular
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Mutagenesis
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Nucleocapsid Proteins / chemistry*
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Nucleocapsid Proteins / genetics
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Nucleocapsid Proteins / ultrastructure
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Protein Conformation
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Protein Structure, Secondary
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Protein Structure, Tertiary
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Protein Subunits / chemistry
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RNA, Viral / chemistry*
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RNA, Viral / ultrastructure
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Vesiculovirus / chemistry*
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Vesiculovirus / physiology
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Vesiculovirus / ultrastructure*
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Viral Matrix Proteins / chemistry*
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Viral Matrix Proteins / ultrastructure
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Virion / chemistry
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Virion / ultrastructure
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Virus Assembly
Substances
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Lipid Bilayers
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M protein, Vesicular stomatitis virus
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Nucleocapsid Proteins
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Protein Subunits
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RNA, Viral
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Viral Matrix Proteins