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Mechanisms for enveloped virus budding: Can some viruses do without an ESCRT?
被引:245
作者:
Chen, Benjamin J.
[1
]
Lamb, Robert A.
[1
,2
]
机构:
[1] Northwestern Univ, Dept Biochem Mol Biol & Cell Biol, Evanston, IL 60208 USA
[2] Northwestern Univ, Howard Hughes Med Inst, Evanston, IL 60208 USA
来源:
关键词:
virus budding;
enveloped virus assembly;
virus exit;
late domain;
ESCRT pathway;
D O I:
10.1016/j.virol.2007.11.008
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Many enveloped viruses complete their replication cycle by forming vesicles that bud from the plasma membrane. Some viruses encode "late" (L) domain motifs that are able to hijack host proteins involved in the vacuolar protein sorting (VPS) pathway, a cellular budding process that gives rise to multivesicular bodies and that is topologically equivalent to virus budding. Although many enveloped viruses share this mechanism, examples of viruses that require additional viral factors and viruses that appear to be independent of the VPS pathway have been identified. Alternative mechanisms for virus budding could involve other topologically similar process such as cell abscission, which occurs following cytokinesis, or virus budding could proceed spontaneously as a result of lipid microdomain accumulation of viral proteins. Further examination of novel virus-host protein interactions and characterization of other enveloped viruses for which budding requirements are currently unknown will lead to a better understanding of the cellular processes involved in virus assembly and budding. (c) 2007 Elsevier Inc. All rights reserved.
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页码:221 / 232
页数:12
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