Author: Hebert, Daniel N.; Molinari, Maurizio
Title: Flagging and Docking: dual roles for N-glycans in protein quality control and cellular proteostasis Cord-id: qesm34su Document date: 2012_10_1
ID: qesm34su
Snippet: Nascent polypeptides entering the endoplasmic reticulum (ER) are covalently modified with pre-assembled oligosaccharides. The terminal glucose and mannose residues are immediately removed after the transfer of the oligosaccharide onto newly synthesized polypeptides. This processing determines whether the polypeptide will be retained in the ER, transported along the secretory pathway, or dislocated across the ER membrane for destruction. Recently, new avenues of research and some issues of contro
Document: Nascent polypeptides entering the endoplasmic reticulum (ER) are covalently modified with pre-assembled oligosaccharides. The terminal glucose and mannose residues are immediately removed after the transfer of the oligosaccharide onto newly synthesized polypeptides. This processing determines whether the polypeptide will be retained in the ER, transported along the secretory pathway, or dislocated across the ER membrane for destruction. Recently, new avenues of research and some issues of controversy have been opened by the discovery that lectin-oligosaccharide interactions stabilize supramolecular complexes between regulators of ER-associated degradation (ERAD). In this Opinion, we propose a unified model that depicts carbohydrates acting both as flags signaling the fitness of a maturing protein, and as docking sites that regulate assembly and stability of the ERAD machinery.
Search related documents:
Co phrase search for related documents- Try single phrases listed below for: 1
Co phrase search for related documents, hyperlinks ordered by date