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Henipavirus Mediated Membrane Fusion Virus Entry and Targeted Therapeutics

机译:肝炎病毒介导的膜融合病毒进入和靶向治疗

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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.
机译:副粘病毒科肝炎病毒目前以亨德拉和尼帕病毒为代表,它们都是近来出现的人畜共患病毒病原体,与澳大利亚,东南亚,印度和孟加拉国的高发病率和高死亡率相关,导致反复爆发。这些被包膜的病毒通过其附着(G)和I类融合(F)包膜糖蛋白的协调活动结合并进入宿主靶细胞。肝炎病毒G糖蛋白与宿主细胞B类ephrin相互作用,触发G的构象改变,从而导致F糖蛋白激活,从而促进膜融合过程。使用最近发表的HeV-G和NiV-G以及其他副粘病毒糖蛋白的结构,我们回顾了介导病毒融合过程必不可少的肝炎病毒包膜糖蛋白的特征,包括受体结合,GF相互作用,F活化,重点是G和破坏病毒感染力的突变。最后,鉴于它们通过靶向G和F糖蛋白抑制HeV和NiV进入的能力,总结了最近针对肝炎病毒介导的疾病的候选疗法。

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