Bose Sayantan, Jardetzky Theodore S, Lamb Robert A
Department of Molecular Biosciences, Northwestern University, Evanston, IL 60208-3500, United States.
Department of Structural Biology and Program in Immunology, Stanford University School of Medicine, Stanford, CA 94305, United States.
Virology. 2015 May;479-480:518-31. doi: 10.1016/j.virol.2015.02.037. Epub 2015 Mar 12.
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.
副粘病毒科包含一些对人类和动物极具危害性且广泛传播的致病病毒。在大多数副粘病毒中,两种病毒膜糖蛋白,即融合蛋白(F)和受体结合蛋白(HN、H或G)介导了一个协同过程,先识别宿主细胞表面分子,随后病毒膜与细胞膜融合,导致病毒核衣壳进入细胞质。F与HN、H或G病毒糖蛋白和宿主分子之间的相互作用对于确定这些病毒的宿主范围、毒力和传播至关重要。最近,原子结构以及生化和生物物理研究,为这两种病毒糖蛋白如何成功与细胞膜上的宿主受体相互作用并启动膜融合过程以进入细胞提供了重要见解。这些研究突出了副粘病毒进入的保守核心机制,为合理的抗病毒药物设计和疫苗开发提供了基础依据。