Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractCarcinogenic and mutagenic properties of chemicals in drinking water    Next AbstractImmunomodulation of cell-mediated cytotoxicity after chronic exposure to vapors »

EMBO J


Title:Cotranslational glycosylation of proteins in systems depleted of protein disulphide isomerase
Author(s):Bulleid NJ; Freedman RB;
Address:"Biological Laboratory, University of Kent, Canterbury, UK"
Journal Title:EMBO J
Year:1990
Volume:9
Issue:11
Page Number:3527 - 3532
DOI: 10.1002/j.1460-2075.1990.tb07561.x
ISSN/ISBN:0261-4189 (Print) 1460-2075 (Electronic) 0261-4189 (Linking)
Abstract:"The role of protein disulphide isomerase (PDI) and other resident proteins of the endoplasmic reticulum (ER) lumen in co- and post-translational modification of secretory proteins has been studied in experiments on translation in vitro. We have devised procedures for extracting the lumenal content proteins of dog pancreas microsomal vesicles by alkaline buffer, or detergent washing, and for reconstitution of the depleted membrane fraction. When microsomal membranes are depleted of content by washing at pH 9.1, they are able to co-translationally glycosylate human interferon-gamma (IFN-gamma) and yeast pro-alpha-factor and the products appear to be identical to those produced by control microsomes. However, when microsomal membranes are depleted of content by washing with saponin they are still able to co-translationally translocate and glycosylate human IFN-gamma, but the products were of higher apparent Mr than those generated by control microsomes. When saponin-washed microsomal membranes were reconstituted with homogeneous protein disulphide isomerase (PDI), the generated vesicles gave the same pattern of co-translationally glycosylated IFN-gamma as saponin-washed microsomal membranes lacking PDI. These results are discussed in relation to the roles of resident ER proteins in co-translational modification; they suggest that PDI is not an essential component of the machinery of co-translational N-glycosylation, but that detergent washing may inactivate or remove some ER glycosidases"
Keywords:"Animals Blotting, Western Cell-Free System Dogs Glycoproteins/*metabolism Glycosylation In Vitro Techniques Interferon-gamma/metabolism Isomerases/*physiology Mating Factor Microsomes/*metabolism Pancreas Peptides/metabolism Precipitin Tests Protein Disul;"
Notes:"MedlineBulleid, N J Freedman, R B eng Research Support, Non-U.S. Gov't England 1990/11/01 EMBO J. 1990 Nov; 9(11):3527-32. doi: 10.1002/j.1460-2075.1990.tb07561.x"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 25-12-2024