| Literature DB >> 29201946 |
Nathanael P Cottam1, Daniel Ungar1.
Abstract
Intra-Golgi retrograde vesicle transport is used to traffic and sort resident Golgi enzymes to their appropriate cisternal locations. An assay was established to investigate the molecular details of vesicle targeting in a cell-free system. Stable cell lines were generated in which the trans-Golgi enzyme galactosyltransferase (GalT) was tagged with either CFP or YFP. Given that GalT is recycled to the cisterna where it is located at steady state, GalT-containing vesicles target GalT-containing cisternal membranes. Golgi membranes were therefore isolated from GalT-CFP expressing cells, while vesicles were prepared from GalT-YFP expressing ones. Incubating CFP-labelled Golgi with YFP-labelled vesicles in the presence of cytosol and an energy regeneration mixture at 37 °C produced a significant increase in CFP-YFP co-localization upon fluorescent imaging of the mixture compared to incubation on ice. The assay was validated to require energy, proteins and physiologically important trafficking components such as Rab GTPases and the conserved oligomeric Golgi tethering complex. This assay is useful for the investigation of both physiological and pathological changes that affect the Golgi trafficking machinery, in particular, vesicle tethering.Entities:
Keywords: Conserved oligomeric Golgi complex; Fluorescent imaging; Galactosyltransferase; Golgi apparatus; Vesicle tethering; Vesicle trafficking
Year: 2017 PMID: 29201946 PMCID: PMC5706631 DOI: 10.21769/BioProtoc.2616
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325