Imaging lysosomal enzyme activity in live cells using self-quenched substrates

• Published in: Analytical biochemistry 2012-05, Vol.424 (2), p.178-183
• Main Authors: Humphries, William H., Payne, Christine K.
• Format: Article
• Language: English
• Subjects: Albumin; Animals; Biological Transport - physiology; Biomarkers - metabolism; bovine serum albumin; Cattle; Cell Line; Chlorocebus aethiops; Endocytosis; Endocytosis - physiology; Endosomes - metabolism; Endosomes - ultrastructure; enzyme activity; Epithelial Cells - metabolism; Epithelial Cells - ultrastructure; Flow Cytometry; fluorescence; Fluorescence microscopy; Fluorescent Dyes; fluorescent labeling; Hydrolases; image analysis; Lipoproteins, LDL - metabolism; Live cell imaging; low density lipoprotein; Lysosomal-Associated Membrane Protein 1 - metabolism; Lysosomes - metabolism; Lysosomes - ultrastructure; Microscopy, Confocal; Microscopy, Fluorescence; Molecular Imaging - methods; nanoparticles; Proteolysis; Self-quenching; Serum Albumin, Bovine - metabolism; Single particle tracking
• ISSN: 0003-2697; 1096-0309
• DOI: 10.1016/j.ab.2012.02.033

Endocytosis, the internalization and transport of extracellular cargo, is an essential cellular process. The ultimate step in endocytosis is the intracellular degradation of extracellular cargo for use by the cell. While live cell imaging and single particle tracking have been well-utilized to study the internalization and transport of cargo, the final degradation step has required separate biochemical assays. We describe the use of self-quenched endocytic cargo to image the intracellular transport and degradation of endocytic cargo directly in live cells. We first outline the fluorescent labeling and quantification of two common endocytic cargos: a protein, bovine serum albumin, and a lipid nanoparticle, low-density lipoprotein. In vitro measurements confirm that self-quenching is a function of the number of fluorophores bound to the protein or particle and that recovery of the fluorescent signal occurs in response to enzymatic degradation. We then use confocal fluorescence microscopy and flow cytometry to demonstrate the use of self-quenched bovine serum albumin with standard fluorescence techniques. Using live cell imaging and single particle tracking, we find that the degradation of bovine serum albumin occurs in an endo-lysosomal vesicle that is positive for LAMP1.