Ligand affinity chromatographic purification of rat liver Golgi endomannosidase
| Autor: | S, Hiraizumi, U, Spohr, R G, Spiro |
|---|---|
| Rok vydání: | 1994 |
| Předmět: |
Male
Macromolecular Substances Molecular Sequence Data Golgi Apparatus Disaccharides Ligands Chromatography Affinity Rats Molecular Weight Kinetics Carbohydrate Sequence Liver alpha-Mannosidase Mannosidases Carbohydrate Conformation Chromatography Gel Animals Electrophoresis Polyacrylamide Gel Chromatography High Pressure Liquid |
| Zdroj: | The Journal of biological chemistry. 269(7) |
| ISSN: | 0021-9258 |
| Popis: | In order to achieve isolation of endo-alpha-D-mannosidase, a Golgi-located processing enzyme that accomplishes deglucosylation of glycoproteins with N-linked carbohydrate units by cleaving the linkage between the glucose-substituted mannose residue and the remainder of the oligosaccharide, we have prepared an affinity matrix (Glc alpha 1--3Man-O-(CH2)8CONH-Affi-Gel 102) containing the derivative of the characteristic disaccharide product of this enzyme. Chromatography of a Triton extract of rat liver Golgi membranes on a column of this gel in the presence of castanospermine to prevent binding of alpha-glucosidases permitted a rapid purification of the endomannosidase (70,000-fold over the homogenate) with a 12% yield. This purified enzyme was free of other processing glycosidases and was completely inhibited by Glc alpha 1--3(1-deoxy)mannojirimycin. Examination of the endomannosidase by SDS-polyacrylamide gel electrophoresis revealed a doublet (M(r) 60,000 and 56,000) with the bands being of approximately equal density. Gel permeation high performance liquid chromatography indicated that in its native form the enzyme has an oligomeric structure (M(r) approximately 560,000) consisting of eight to ten subunits. |
| Databáze: | OpenAIRE |
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