Zhang Wei, Cao Sheng, Martin Jessica L, Mueller Joachim D, Mansky Louis M
Institute for Molecular Virology, University of Minnesota, Minneapolis, MN, USA ; Department of Diagnostic and Biological Sciences, School of Dentistry, University of Minnesota, Minneapolis, MN, USA ; Characterization Facility, University of Minnesota, Minneapolis, MN, USA.
Wuhan Institute of Virology, Chinese Academy of Science, Wuhan, China.
AIMS Biophys. 2015;2(3):343-369. doi: 10.3934/biophy.2015.3.343. Epub 2015 Aug 18.
Retrovirus morphogenesis entails assembly of Gag proteins and the viral genome on the host plasma membrane, acquisition of the viral membrane and envelope proteins through budding, and formation of the core through the maturation process. Although in both immature and mature retroviruses, Gag and capsid proteins are organized as paracrystalline structures, the curvatures of these protein arrays are evidently not uniform within one or among all virus particles. The heterogeneity of retroviruses poses significant challenges to studying the protein contacts within the Gag and capsid lattices. This review focuses on current understanding of the molecular organization of retroviruses derived from the sub-nanometer structures of immature virus particles, helical capsid protein assemblies and soluble envelope protein complexes. These studies provide insight into the molecular elements that maintain the stability, flexibility and infectivity of virus particles. Also reviewed are morphological studies of retrovirus budding, maturation, infection and cell-cell transmission, which inform the structural transformation of the viruses and the cells during infection and viral transmission, and lead to better understanding of the interplay between the functioning viral proteins and the host cell.
逆转录病毒形态发生需要Gag蛋白和病毒基因组在宿主质膜上组装,通过出芽获得病毒膜和包膜蛋白,并通过成熟过程形成核心。尽管在未成熟和成熟的逆转录病毒中,Gag蛋白和衣壳蛋白都组织成准晶体结构,但这些蛋白质阵列的曲率在单个或所有病毒颗粒之间显然并不均匀。逆转录病毒的异质性给研究Gag和衣壳晶格内的蛋白质接触带来了重大挑战。本综述重点关注目前对逆转录病毒分子组织的理解,这些理解源自未成熟病毒颗粒、螺旋衣壳蛋白组装体和可溶性包膜蛋白复合物的亚纳米结构。这些研究为维持病毒颗粒稳定性、灵活性和感染性的分子元件提供了见解。还综述了逆转录病毒出芽、成熟、感染和细胞间传播的形态学研究,这些研究揭示了感染和病毒传播过程中病毒和细胞的结构转变,并有助于更好地理解功能性病毒蛋白与宿主细胞之间的相互作用。