Arranz Rocío, Chichón Francisco Javier, Cuervo Ana, Conesa José Javier
Department of Macromolecular Structure, Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.
Subcell Biochem. 2024;105:299-327. doi: 10.1007/978-3-031-65187-8_8.
Understanding the dynamic processes involving virus structural components within host cells is crucial for comprehending viral infection, as viruses rely entirely on host cells for replication. Viral infection involves various intracellular stages, including cell entry, genome uncoating, replication, transcription and translation, assembly of new virus particles in a complex morphogenetic process, and the release of new virions from the host cell. These events are dynamic and scarce and can be obscured by other cellular processes, necessitating novel approaches for their in situ characterization. Among these methods, correlative microscopy integrates the labeling, localization, and functional characterization of events of interest through visible light microscopy, complemented by the structural insights provided by high-resolution imaging techniques. This correlative approach enables a comprehensive exploration of subcellular events within the cellular context, including those related to viral morphogenesis. This chapter provides an introduction to correlative three-dimensional imaging methods, specifically designed to study viral morphogenesis and other intracellular stages of the viral cycle under conditions closely resembling their native environment. The integration of whole-cell imaging and high-resolution structural biology techniques is emphasized as essential for unraveling the mechanisms by which viruses generate and disseminate their progeny.
了解宿主细胞内涉及病毒结构成分的动态过程对于理解病毒感染至关重要,因为病毒完全依赖宿主细胞进行复制。病毒感染涉及多个细胞内阶段,包括细胞进入、基因组脱壳、复制、转录和翻译、在复杂的形态发生过程中组装新的病毒颗粒,以及从宿主细胞释放新的病毒粒子。这些事件动态且稀少,可能会被其他细胞过程掩盖,因此需要新的方法对其进行原位表征。在这些方法中,相关显微镜通过可见光显微镜整合了感兴趣事件的标记、定位和功能表征,并辅以高分辨率成像技术提供的结构见解。这种相关方法能够在细胞环境中全面探索亚细胞事件,包括与病毒形态发生相关的事件。本章介绍了相关三维成像方法,这些方法专门设计用于在与天然环境非常相似的条件下研究病毒形态发生和病毒周期的其他细胞内阶段。强调了全细胞成像和高分辨率结构生物学技术的整合对于揭示病毒产生和传播后代的机制至关重要。