Unit

UNIT 12.4 Endoglycosidase and Glycoamidase Release of N-Linked Oligosaccharides

  1. Hudson H. Freeze,
  2. Christian Kranz

Published Online: 1 SEP 2006

DOI: 10.1002/0471140864.ps1204s45

Current Protocols in Protein Science

Current Protocols in Protein Science

How to Cite

Freeze, H. H. and Kranz, C. 2006. Endoglycosidase and Glycoamidase Release of N-Linked Oligosaccharides. Current Protocols in Protein Science. 45:12.4:12.4.1–12.4.26.

Author Information

  1. The Burnham Institute, La Jolla, California

Publication History

  1. Published Online: 1 SEP 2006
  2. Published Print: AUG 2006

This is not the most recent version of the article. View current version (1 NOV 2010)

Abstract

Nearly all proteins entering the lumen of the endoplasmic reticulum (ER) become glycosylated en route to a cellular organelle, the plasma membrane, or the extracellular space. Many glycans can be attached to proteins, but the most common are the N-linked oligosaccharides. These chains are added very soon after a protein enters the ER, but they undergo extensive remodeling (processing), especially in the Golgi. Processing changes the sensitivity of the N-glycan to enzymes that cleave entire sugar chains or individual monosaccharides, which also changes the migration of the protein on SDS gels. These changes can be used to indicate when a protein has passed a particular subcellular location. This unit details some of the methods used to track a protein as it traffics from the ER to the Golgi toward its final location.

Keywords:

  • glycosylation;
  • oligosaccharide processing;
  • Golgi;
  • endoplasmic reticulum;
  • pulse-chase;
  • metabolic labeling;
  • post-translational modification;
  • deglycosylation