Mapping localization of 21 endogenous proteins in the Golgi apparatus of rodent neurons

• Published in: Scientific reports Vol. 13; no. 1; p. 2871
• Main Authors: van Bommel, Danique M., Toonen, Ruud F., Verhage, Matthijs
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 18-02-2023; Nature Publishing Group; Nature Portfolio
• Subjects: 631/1647/328/1978; 631/80/642/1525; Animals; Cell Line; Cell lines; Cell Movement; Confocal microscopy; Golgi Apparatus; Humanities and Social Sciences; Knowledge; Localization; Mice; multidisciplinary; Neurons; Peptide mapping; Protein transport; Proteins; Science; Science (multidisciplinary); Upstream
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-023-29998-8

The Golgi apparatus is the major sorting hub in the secretory pathway and particularly important for protein sorting in neurons. Knowledge about protein localization in Golgi compartments is largely based on work in cell lines. Here, we systematically compared protein localization of 21 endogenous proteins in the Golgi apparatus of mouse neurons using confocal microscopy and line scan analysis. We localized these proteins by measuring the distance relative to the canonical TGN marker TGN38. Based on this, proteins fell into three groups: upstream of, overlapping with or downstream of TGN38. Seven proteins showed complete overlap with TGN38, while proteins downstream of TGN38 were located at varying distances from TGN38. Proteins upstream of TGN38 were localized in between TGN38 and the
cis
-/medial Golgi markers Giantin and GM130. This localization was consistent with protein function. Our data provide an overview of the relative localization of endogenous proteins in the Golgi of primary mouse neurons.