Henipavirus Mediated Membrane Fusion, Virus Entry and Targeted Therapeutics

被引:45
|
作者
Steffen, Deborah L. [1 ]
Xu, Kai [2 ]
Nikolov, Dimitar B. [2 ]
Broder, Christopher C. [1 ]
机构
[1] Uniformed Serv Univ Hlth Sci, Dept Microbiol & Immunol, Bethesda, MD 20814 USA
[2] Mem Sloan Kettering Canc Ctr, Struct Biol Program, New York, NY 10021 USA
来源
VIRUSES-BASEL | 2012年 / 4卷 / 02期
基金
美国国家卫生研究院;
关键词
paramyxovirus; entry; attachment glycoprotein; fusion glycoprotein; membrane fusion; receptor; ephrin-B2; ephrin-B3; inhibitor; antibody; immunotherapy; TO-PERSON TRANSMISSION; NIPAH-VIRUS; HENDRA-VIRUS; ATTACHMENT GLYCOPROTEIN; PARAMYXOVIRUS FUSION; RECEPTOR-BINDING; CLINICAL-FEATURES; CRYSTAL-STRUCTURE; AMINO-ACID; F-PROTEIN;
D O I
10.3390/v4020280
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The Paramyxoviridae genus Henipavirus is presently represented by the type species Hendra and Nipah viruses which are both recently emerged zoonotic viral pathogens responsible for repeated outbreaks associated with high morbidity and mortality in Australia, Southeast Asia, India and Bangladesh. These enveloped viruses bind and enter host target cells through the coordinated activities of their attachment (G) and class I fusion (F) envelope glycoproteins. The henipavirus G glycoprotein interacts with host cellular B class ephrins, triggering conformational alterations in G that lead to the activation of the F glycoprotein, which facilitates the membrane fusion process. Using the recently published structures of HeV-G and NiV-G and other paramyxovirus glycoproteins, we review the features of the henipavirus envelope glycoproteins that appear essential for mediating the viral fusion process, including receptor binding, G-F interaction, F activation, with an emphasis on G and the mutations that disrupt viral infectivity. Finally, recent candidate therapeutics for henipavirus-mediated disease are summarized in light of their ability to inhibit HeV and NiV entry by targeting their G and F glycoproteins.
引用
收藏
页码:280 / 308
页数:29
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