Free N-linked oligosaccharide chains: Formation and degradation
- 1 July 2006
- journal article
- review article
- Published by Springer Nature in Glycoconjugate Journal
- Vol. 23 (5) , 291-302
- https://doi.org/10.1007/s10719-006-6975-x
Abstract
There is growing evidence that N-linked glycans play pivotal roles in protein folding and intra- and/or intercellular trafficking of N-glycosylated proteins. It has been shown that during the N-glycosylation of proteins, significant amounts of free oligosaccharides (free OSs) are generated in the lumen of the endoplasmic reticulum (ER) by a mechanism which remains to be clarified. Free OSs are also formed in the cytosol by enzymatic deglycosylation of misfolded glycoproteins, which are subjected to destruction by a cellular system called “ER-associated degradation (ERAD).” While the precise functions of free OSs remain obscure, biochemical studies have revealed that a novel cellular process enables them to be catabolized in a specialized manner, that involves pumping free OSs in the lumen of the ER into the cytosol where further processing occurs. This process is followed by entry into the lysosomes. In this review we summarize current knowledge about the formation, processing and degradation of free OSs in eukaryotes and also discuss the potential biological significance of this pathway. Other evidence for the occurrence of free OSs in various cellular processes is also presented.Keywords
This publication has 138 references indexed in Scilit:
- A genome‐wide screen identifies Yos9p as essential for ER‐associated degradation of glycoproteinsFEBS Letters, 2004
- Endoplasmic reticulum-associated degradation: exceptions to the ruleEuropean Journal of Cell Biology, 2004
- The PUB Domain: A Putative Protein–Protein Interaction Domain Implicated in the Ubiquitin-Proteasome PathwayBiochemical and Biophysical Research Communications, 2001
- Identification of Peptide:N-Glycanase Activity in Mammalian-Derived Cultured CellsBiochemical and Biophysical Research Communications, 1993
- Identification of free glycan chain liberated by de-N-glycosylation of the cortical alveolar glycopolyprotein (hyosophorin) during early embryogenesis of the Medaka fish, Oryzias latipesBiochemical and Biophysical Research Communications, 1991
- Isolation and characterization of free glycans of the oligomannoside type from the extracellular medium of a plant cell suspensionGlycoconjugate Journal, 1990
- Demonstration of a new glycopeptidase, from jack-bean meal, acting on aspartylglucosylamine linkagesBiochemical and Biophysical Research Communications, 1983
- Demonstration of a new amidase acting on glycopeptidesBiochemical and Biophysical Research Communications, 1977
- Endo-β-N-acetylglucosaminidase from fig latexBiochemical and Biophysical Research Communications, 1977
- Endoglycosidases acting on carbohydrate moieties of glycoproteins: Demonstration in mammalian tissueBiochemical and Biophysical Research Communications, 1974