Unit
UNIT 12.4 Endoglycosidase and Glycoamidase Release of N-Linked Oligosaccharides
Published Online: 1 SEP 2006
DOI: 10.1002/0471140864.ps1204s45
Copyright © 2006 by John Wiley & Sons, Inc.
Lab Protocol Title

Current Protocols in Protein Science
Additional Information
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.
Publication History
- Published Online: 1 SEP 2006
- 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
