Timing is everything: Fine-tuned molecular machines orchestrate paramyxovirus entry

被引:86
作者
Bose, Sayantan [1 ]
Jardetzky, Theodore S. [3 ,4 ]
Lamb, Robert A. [1 ,2 ]
机构
[1] Northwestern Univ, Dept Mol Biosci, Evanston, IL 60208 USA
[2] Northwestern Univ, Howard Hughes Med Inst, Evanston, IL 60208 USA
[3] Stanford Univ, Sch Med, Dept Biol Struct, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Program Immunol, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
Membrane fusion; Membrane glycoproteins; Viral envelope proteins; Paramyxovirus entry; Atomic structure of viral glycoproteins; Viral receptors; Fusion protein; NEWCASTLE-DISEASE VIRUS; RESPIRATORY SYNCYTIAL VIRUS; HEMAGGLUTININ-NEURAMINIDASE PROTEIN; RECEPTOR-BINDING SITE; TISSUE-CULTURE CELLS; 5 FUSION PROTEIN; MORBILLIVIRUS ATTACHMENT PROTEIN; HUMAN METAPNEUMOVIRUS LACKING; TRIGGERS MEMBRANE-FUSION; AMINO-ACID SUBSTITUTIONS;
D O I
10.1016/j.virol.2015.02.037
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
The Paramyxoviridae include some of the great and ubiquitous disease-causing viruses of humans and animals. In most paramyxoviruses, two viral membrane glycoproteins, fusion protein (F) and receptor binding protein (HN, H or G) mediate a concerted process of recognition of host cell surface molecules followed by fusion of viral and cellular membranes, resulting in viral nucleocapsid entry into the cytoplasm. The interactions between the F and HN, H or G viral glycoproteins and host molecules are critical in determining host range, virulence and spread of these viruses. Recently, atomic structures, together with biochemical and biophysical studies, have provided major insights into how these two viral glycoproteins successfully interact with host receptors on cellular membranes and initiate the membrane fusion process to gain entry into cells. These studies highlight the conserved core mechanisms of paramyxovirus entry that provide the fundamental basis for rational anti-viral drug design and vaccine development. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:518 / 531
页数:14
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