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PMID: 1847682 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Purification, biosynthesis and cellular localization of a major 125-kDa glycophosphatidylinositol-anchored membrane glycoprotein of Saccharomyces cerevisiae.

European journal of biochemistry ·Vol. 195 ·No. 2 ·1991-01-30 ·Pages 439-48

Fankhauser C, Conzelmann A

Abstract

The yeast Saccharomyces cerevisiae has been shown to contain a major 125-kDa membrane glycoprotein which is anchored in the lipid bilayer by a glycophosphatidylinositol anchor. This protein was purified to near homogeneity and was used to raise a rabbit antibody. Biosynthesis of the 125-kDa protein was studied by immunoprecipitation of 35SO4-labeled material from wild-type cells or a secretion mutant (sec18) in which the vesicular traffic from the endoplasmic reticulum (ER) to the Golgi is blocked. The 125-kDa protein is first made in the ER as a 105-kDa precursor which already contains a glycophosphatidylinositol anchor and which is slowly transformed into the 125-kDa form upon chase (t1/2 approximately 10-15 min). The 105-kDa precursor can be reduced to an 83-kDa form by the enzymatic removal of N-glycans. The removal of N-glycans from the mature 125-kDa protein yields a 95-kDa species. Thus, removal of the N-glycans does not reduce the ER and mature forms to the same molecular mass, indicating that not only elongation of N-glycans but also another post-translational modification takes place during maturation. Selective tagging of surface proteins by treatment of 35SO4-labeled cells with trinitrobenzene sulfonic acid at 0 C followed by immunoprecipitation of the tagged proteins shows that the 125-kDa protein, but not the 105-kDa precursor, becomes transported to the cell surface. This tagging of cells after various lengths of chase also shows that the surface appearance of the protein is biphasic with about one half of the mature 125-kDa protein remaining intracellular for over 2 h. Glycosylation and/or glycophosphatidylinositol anchor addition is important for the stability of the 125-kDa protein since the protein remains undetectable in sec53, a temperature-sensitive mutant which does not make GDP-mannose at 37 C and does not add glycophosphatidylinositol anchors at 37 degrees C.

MeSH Terms
Antibodies/immunology Biological Transport Cell Membrane/chemistry Endoplasmic Reticulum/metabolism Glycolipids/immunology,metabolism Glycoproteins/metabolism Glycosylation Glycosylphosphatidylinositols Golgi Apparatus/metabolism Hydrolysis Kinetics Lipid Bilayers/chemistry Molecular Weight Phosphatidylinositol Diacylglycerol-Lyase Phosphatidylinositols/immunology,metabolism Phosphoric Diester Hydrolases/pharmacology Polysaccharides/isolation & purification Saccharomyces cerevisiae/drug effects,metabolism Sensitivity and Specificity Trinitrobenzenesulfonic Acid/pharmacology
Chemicals
Antibodies Glycolipids Glycoproteins Glycosylphosphatidylinositols Lipid Bilayers Phosphatidylinositols Polysaccharides Trinitrobenzenesulfonic Acid Phosphoric Diester Hydrolases Phosphatidylinositol Diacylglycerol-Lyase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Fankhauser C
Institute of Biochemistry, University of Lausanne, Epalinges, Switzerland.
Conzelmann A
Article Info
Journal
European journal of biochemistry
Abbr.
Eur J Biochem
ISSN
0014-2956
Published
1991-01-30
Pages
439-48
Language
English
Region
England
NLM ID
0107600
Subset
IM
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