Kacal Merve, Vakifahmetoglu-Norberg Helin
Department of Physiology and Pharmacology, Solnavägen 9, Biomedicum, Karolinska Institutet, Stockholm, Sweden.
Methods Mol Biol. 2022;2445:27-38. doi: 10.1007/978-1-0716-2071-7_2.
Accurate isolation of functional and intact lysosomes enables the quantification and analyses of abundances, dynamic changes and enrichment levels of lysosomal content, allowing specific lysosomal investigations induced by autophagy. In this protocol chapter, we describe detailed practical instructions and advices for an efficacious lysosomal enrichment and isolation procedure by differential multilayered density gradient centrifugations using human cancer cell lines. By this method, intact and autophagy competent lysosomes can be isolated from cancer cells based on their distinct density and obtained fractions can further be analyzed for functional lysosomal assays, as well as for protein or metabolic loads to identify select spatiotemporal changes by comparative quantitative measurement. This method has been used to enrich lysosomes from a variety of cancer cells with activated chaperone-mediated autophagy, but can be optimized for other cell lines and tissues for multiple autophagy-induced conditions.
准确分离功能完整的溶酶体能够对溶酶体内容物的丰度、动态变化和富集水平进行定量和分析,从而实现对自噬诱导的特定溶酶体的研究。在本实验方案章节中,我们描述了使用人类癌细胞系通过差异多层密度梯度离心进行有效溶酶体富集和分离程序的详细操作说明和建议。通过这种方法,可以根据其不同的密度从癌细胞中分离出完整且具有自噬能力的溶酶体,所得组分可进一步用于功能性溶酶体分析,以及蛋白质或代谢负荷分析,以通过比较定量测量来识别特定的时空变化。该方法已用于从多种具有激活的伴侣介导自噬的癌细胞中富集溶酶体,但可针对其他细胞系和组织在多种自噬诱导条件下进行优化。