The Pirbright Institute, Woking, UK.
The Francis Crick Institute, London, UK.
Methods Mol Biol. 2024;2838:91-100. doi: 10.1007/978-1-0716-4035-7_5.
The confocal laser scanning microscope allows the visualization of intracellular structures in greater detail than a widefield fluorescence microscope. Immunofluorescence (IF) techniques make use of the inherent ability of antibodies to bind to specific epitopes of specific proteins. Tagging these antibodies with an easily visualized molecule, e.g., a fluorophore, enables imaging in the fluorescence microscope. This is, however, a localization technique and will only give information about where certain proteins are; it does not provide the ultrastructural context provided by the transmission electron microscope. It also relies heavily on the accuracy and binding affinity of individual primary antibodies. Despite this, it is a commonly used, robust, and adaptable technique. In this chapter, we use a long-established IF protocol from our laboratory to locate EHDV proteins in a monolayer of infected cultured cells.
共聚焦激光扫描显微镜能够比宽场荧光显微镜更详细地观察细胞内结构。免疫荧光(IF)技术利用抗体结合特定蛋白质特定表位的固有能力。通过将这些抗体与易于可视化的分子(例如荧光团)标记,可在荧光显微镜中进行成像。但是,这是一种定位技术,只能提供有关特定蛋白质所在位置的信息;它不能提供透射电子显微镜提供的超微结构背景。它还严重依赖于单个一抗的准确性和结合亲和力。尽管如此,它仍是一种常用的、强大的、适应性强的技术。在本章中,我们使用来自我们实验室的一种成熟的 IF 方案,在单层感染的培养细胞中定位 EHDV 蛋白。