Marín Josefina, Aguilera Paulina, Lagos Rosalba, Marcoleta Andrés
Laboratorio de Biología Estructural y Molecular BEM, Departamento de Biología, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
Methods Mol Biol. 2022;2538:261-273. doi: 10.1007/978-1-0716-2529-3_17.
Although amyloid aggregation has been generally associated with protein misfolding and neurodegenerative diseases in mammals, bacteria and other organisms have harnessed amyloidogenesis to perform diverse biological processes. These functional amyloids, some of them secreted and others intracellular, require that the producing cells keep aggregation under control in the cytoplasm upon protein translation, preventing their inherent toxicity. Thus, it is highly relevant to understand how intracellular amyloid formation occurs and is regulated, its metabolic consequences, and the formation dynamics and fate of the amyloid inclusions upon cell division. This chapter describes methods leveraging fluorescence microscopy and fixed- or live-cell imaging to monitor intracellular amyloid formation in bacterial cells.
尽管淀粉样蛋白聚集通常与哺乳动物、细菌和其他生物体中的蛋白质错误折叠及神经退行性疾病相关,但细菌和其他生物体已利用淀粉样蛋白生成来执行多种生物学过程。这些功能性淀粉样蛋白,有些是分泌型的,有些是细胞内型的,要求产生细胞在蛋白质翻译时将聚集控制在细胞质中,防止其固有的毒性。因此,了解细胞内淀粉样蛋白如何形成和受到调控、其代谢后果以及细胞分裂时淀粉样蛋白内含物的形成动态和命运具有高度相关性。本章介绍了利用荧光显微镜以及固定细胞或活细胞成像来监测细菌细胞内淀粉样蛋白形成的方法。