un-“escrt”-ed budding
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ID: 221556
2011
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Abstract
In their recent publication, Rossman et al. [1] describe how the inherent budding capability of its M2 protein allows influenza A virus to bypass recruitment of the cellular ESCRT machinery enlisted by several other enveloped RNA and DNA viruses, including HIV, Ebola, rabies, herpes simplex type 1 and hepatitis B. Studies from the same laboratory [2] and other laboratories [3–6] indicate that budding of plasmid-derived virus-like particles can be mediated by the influenza virus hemagglutinin and neuraminidase proteins in the absence of M2. These events are also independent of canonical ESCRT components [2,7]. Understanding how intrinsic properties of these influenza virus proteins permit ESCRT-independent budding expands our understanding of the budding process itself.
| Reference Key |
yondola2011virusesun-escrt-ed
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|---|---|
| Authors | ;Mark Yondola;Carol Carter |
| Journal | International journal of pharmaceutics |
| Year | 2011 |
| DOI |
10.3390/v3010026
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| URL | |
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