Sachse Martin, de Castro Isabel Fernández, Fournier Guillaume, Naffakh Nadia, Risco Cristina
Institut Pasteur, Ultrapole, Paris, France.
Centro Nacional de Biotecnologia, CNB-CSIC, Cell Structure Lab, Madrid, Spain.
Methods Mol Biol. 2018;1836:281-301. doi: 10.1007/978-1-4939-8678-1_14.
Transmission electron microscopy (TEM) has been instrumental for studying viral infections. In particular, methods for labeling macromolecules at the ultrastructural level, by integrating biochemistry, molecular biology, and morphology, have allowed to study the functions of viral macromolecular complexes within the cellular context. Here, we describe a strategy for imaging influenza virus ribonucleoproteins in infected cells with two complementary labeling methods, metal-tagging transmission electron microscopy or METTEM, a highly sensitive technique based on the use of a metal-binding protein as a clonable tag, and immunogold labeling on thawed cryosections, a very specific labeling method that allows to study the distribution of different proteins simultaneously. The combination of both labeling methods offers new possibilities for TEM analysis of viral components in cells.
透射电子显微镜(TEM)在研究病毒感染方面发挥了重要作用。特别是,通过整合生物化学、分子生物学和形态学,在超微结构水平上标记大分子的方法,使得在细胞环境中研究病毒大分子复合物的功能成为可能。在这里,我们描述了一种用两种互补标记方法对感染细胞中的流感病毒核糖核蛋白进行成像的策略,即金属标记透射电子显微镜(METTEM),这是一种基于使用金属结合蛋白作为可克隆标签的高灵敏度技术,以及在解冻的冷冻切片上进行免疫金标记,这是一种非常特异的标记方法,可同时研究不同蛋白质的分布。这两种标记方法的结合为细胞中病毒成分的TEM分析提供了新的可能性。