Histodenz Separation of Lysosomal Subpopulations for Analysis of Chaperone‐mediated Autophagy

Abstract

AbstractChaperone‐mediated autophagy (CMA) is the most selective form of lysosomal proteolysis, in which proteins are individually selected for lysosomal degradation. CMA degradation targets bear a pentapeptide consensus motif that is recognized by the cytosolic chaperone HSPA8 (Hsc70), which participates in the trafficking of the target to the lysosomal surface. From there, it is translocated into the lysosomal lumen, independent of vesicle fusion, in a process dependent upon the lysosomal transmembrane protein LAMP2A. There are limited tools for studying CMA in whole cells and tissues, and many of the best techniques for studying CMA rely on the preparation of lysosome enriched fractions. Such experiments include (1) the in vitro evaluation of CMA substrate uptake activity, (2) the characterization of changes to lysosomal resident and CMA regulatory proteins, and (3) lysosomal targetomics, i.e., the use of quantitative proteomics to characterize lysosomal degradation targets. Previous studies using discontinuous metrizamide gradients have shown that a subpopulation of liver lysosomes is responsible for the majority of CMA activity (“CMA+”). These CMA+ lysosomes are low density and have higher levels of MTORC2 relative to the “CMA–” lysosomes, which are high density and have higher levels of MTORC1. Because of safety concerns surrounding metrizamide, however, this compound is difficult to obtain, and it is impractically expensive. Here, we have provided protocols for isolation of lysosomal subpopulations for CMA‐related analyses from mouse liver using Histodenz, a safe and affordable alternative to metrizamide. Supplementary protocols show how to perform CMA activity assays with appropriate statistical analysis, and how to analyze for lysosomal breakage/membrane integrity. © 2024 The Authors. Current Protocols published by Wiley Periodicals LLC.Basic Protocol: Isolation of lysosomal subpopulations from mouse liver using discontinuous Histodenz gradientsAlternate Protocol: Isolation of lysosomes from cultured cells using discontinuous Histodenz gradientsSupport Protocol 1: Verifying enrichment of lysosomal markers in lysosome‐enriched fractionsSupport Protocol 2: Measuring in vitro uptake of CMA substratesSupport Protocol 3: Measuring lysosomal membrane integrity by hexosaminidase assay