Keene Douglas R, Tufa Sara F
Shriners Hospitals for Children, Micro-Imaging Center, Portland, OR, United States.
Shriners Hospitals for Children, Micro-Imaging Center, Portland, OR, United States.
Methods Cell Biol. 2018;143:1-39. doi: 10.1016/bs.mcb.2017.08.002. Epub 2017 Oct 25.
This chapter gives insight into task-specific methodologies for the evaluation of matrix ultrastructure by light and electron microscopy. It separately considers the isolation and preparation of molecular isolates for negative staining, immunolabeling, rotary shadowing, and single particle analysis. Also considered is the preparation of whole tissues and cultured cells by chemical fixation and cryofixation methodologies. Immunoelectron microscopy for immunoidentification of matrix components may be accomplished en bloc or via section-surface protocols; the advantages and pitfalls in both methodologies are described. Correlative light and electron microscopy, particularly utilizing GFP constructs, demands special consideration in fixation and embedding protocols. TEM imaging methods, including the use of montage software and the acquisition of thick-section tilt series are discussed. The protocols presented in this chapter, with the exception of single particle analysis, are those which are continuously used in our laboratory and represent the latest modifications in our protocols.
本章深入介绍了通过光学显微镜和电子显微镜评估基质超微结构的特定任务方法。它分别考虑了用于负染色、免疫标记、旋转阴影和单颗粒分析的分子分离物的分离和制备。还考虑了通过化学固定和冷冻固定方法制备全组织和培养细胞。用于基质成分免疫鉴定的免疫电子显微镜可以整体完成或通过切片表面方案完成;描述了两种方法的优点和陷阱。相关光镜和电镜,特别是利用绿色荧光蛋白构建体的情况,在固定和包埋方案中需要特别考虑。讨论了透射电镜成像方法,包括使用拼接软件和获取厚切片倾斜系列。本章介绍的方案,除了单颗粒分析外,都是我们实验室一直在使用的,代表了我们方案的最新改进。