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
相关论文
共 50 条
  • [21] Exploiting Herpes Simplex Virus Entry for Novel Therapeutics
    Hadigal, Satvik
    Shukla, Deepak
    VIRUSES-BASEL, 2013, 5 (06): : 1447 - 1465
  • [22] Vaccinia virus L1 protein is required for cell entry and membrane fusion
    Bisht, Himani
    Weisberg, Andrea S.
    Moss, Bernard
    JOURNAL OF VIROLOGY, 2008, 82 (17) : 8687 - 8694
  • [23] In fiuenza a Virus Entry Implications in Virulence and Future Therapeutics
    Rumschlag-Booms, Emily
    Rong, Lijun
    ADVANCES IN VIROLOGY, 2013, 2013
  • [24] Entry and fusion of La Crosse virus
    Hollidge, Bradley S.
    Soldan, Samantha S.
    Wagner, Valentia
    Weber, Friedmann
    Gonzalez-Scarano, Francisco
    JOURNAL OF NEUROVIROLOGY, 2010, 16 : 37 - 38
  • [25] Virus membrane fusion
    Weissenhorn, Winfried
    Hinz, Andreas
    Gaudin, Yves
    FEBS LETTERS, 2007, 581 (11) : 2150 - 2155
  • [26] Structural Insights into the Membrane Fusion Mechanism Mediated by Influenza Virus Hemagglutinin
    Ni, Fengyun
    Chen, Xiaorui
    Shen, Jun
    Wang, Qinghua
    BIOCHEMISTRY, 2014, 53 (05) : 846 - 854
  • [27] Imaging Multiple Intermediates of Single-Virus Membrane Fusion Mediated by Distinct Fusion Proteins
    Joo, Kye-Il
    Tai, April
    Lee, Chi-Lin
    Wong, Clement
    Wang, Pin
    MICROSCOPY RESEARCH AND TECHNIQUE, 2010, 73 (09) : 886 - 900
  • [28] Influenza Virus-Mediated Membrane Fusion: Determinants of Hemagglutinin Fusogenic Activity and Experimental Approaches for Assessing Virus Fusion
    Hamilton, Brian S.
    Whittaker, Gary R.
    Daniel, Susan
    VIRUSES-BASEL, 2012, 4 (07): : 1144 - 1168
  • [29] Palmitoylation Contributes to Membrane Curvature in Influenza A Virus Assembly and Hemagglutinin-Mediated Membrane Fusion
    Chlanda, Petr
    Mekhedov, Elena
    Waters, Hang
    Sodt, Alexander
    Schwartz, Cindi
    Nair, Vinod
    Blank, Paul S.
    Zimmerberg, Joshua
    JOURNAL OF VIROLOGY, 2017, 91 (21)
  • [30] Aptamer-Mediated Targeted Delivery of Therapeutics: An Update
    Catuogno, Silvia
    Esposito, Carla L.
    de Franciscis, Vittorio
    PHARMACEUTICALS, 2016, 9 (04)