A Review of Reagents for Fluorescence Microscopy of Cellular Compartments and Structures, Part I: BacMam Labeling and Reagents for Vesicular Structures
Nick J. Dolman, Jason A. Kilgore- Medical Laboratory Technology
- Health Informatics
- General Pharmacology, Toxicology and Pharmaceutics
- General Immunology and Microbiology
- General Biochemistry, Genetics and Molecular Biology
- General Neuroscience
Abstract
Fluorescent labeling of vesicular structures in cultured cells, particularly for live cells, can be challenging for a number of reasons. The first challenge is to identify a reagent that will be specific enough where some structures have a number of potential reagents and others very few options. The emergence of BacMam constructs has provided more easy‐to‐use choices. Presented here is a discussion of BacMam constructs as well as a review of commercially available reagents for labeling vesicular structures in cells, including endosomes, peroxisomes, lysosomes, and autophagosomes, complete with a featured reagent, recommended protocol, troubleshooting guide, and example image for each structure. © 2023 Wiley Periodicals LLC.
Basic Protocol 1: Delivering targeted fluorescent proteins using pre‐made, high‐titer BacMam constructs
Alternate Protocol 1: Non‐pseudo‐typed BacMam viruses in standard cell types and pseudo‐typed BacMam viruses in hard‐to‐transduce cell types
Basic Protocol 2: Labeling endosomes: pHrodo™‐10k‐dextran
Basic Protocol 3: Labeling peroxisomes: BacMam 2.0 CellLight™ Peroxisome‐GFP
Alternate Protocol 2: Labeling peroxisomes using antibodies
Basic Protocol 4: Labeling autophagosomes: Transduction of cells with Premo™ Autophagy Sensor GFP‐LC3B
Alternate Protocol 3: Labeling autophagosomes using antibodies
Basic Protocol 5: Labeling lysosomes: LysoTracker Red DND‐99