Title of article :
The glycans of horseradish peroxidase
Author/Authors :
Byung Yun Yang، نويسنده , , James S.S. Gray، نويسنده , , Rex Montgomery، نويسنده ,
Issue Information :
دوهفته نامه با شماره پیاپی سال 1996
Pages :
10
From page :
203
To page :
212
Abstract :
Horseradish peroxidase (E.C. 1.11.1.7) isozyme c (HRPc) is a glycoprotein found to contain 21.8% carbohydrate with the average composition: 2 mol GlcNAc, 2.6 mol Man, and 0.8 mol each of Fuc and Xyl. The oligosaccharides of HRPc were investigated by a combination of High pH Anion-Exchange Chromatography with Pulsed Amperometric Detection, methylation analysis and Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry. The structure of the major oligosaccharide released by digestion with glycopeptidase A, accounting for between 75 and 80% of the total, was confirmed to be α-Man-(1 → 6)[α-Man-(1 → 3)][β-Xyl-(1 → 2)]-β-Man-(1 → 4)-β-GlcNAc-(1 → 4)[α-Fuc-(1 → 3)]-GlcNAc. Most of the remaining oligosaccharides were found to belong to the (Xyl)xManm(Fuc)fGlcNAc2 (m = 2, 4, 5, 6; f = 0 or 1; x = 0 or 1) family. Less than 5% of the oligosaccharides were of the ManmGlcNAc2 (m = 4 to 7) type. Methylation analysis of holo- and apo-HRPc and its tryptic glycopeptides support the structures proposed for the oligosaccharides. Furthermore, methylation analysis of the tryptic glycopeptides provides evidence for the heterogeneity of the oligosaccharides occurring at each of the N-linked sites.
Keywords :
Glycan , Horseradish peroxidase , Methylation analysis , N-linked oligosaccharides , MALDITOF
Journal title :
Carbohydrate Research
Serial Year :
1996
Journal title :
Carbohydrate Research
Record number :
961462
Link To Document :
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