Title of article
Structural Analysis on the Sugar Chains of Human α1-Antitrypsin: Presence of Fucosylated Biantennary Glycan in Hepatocellular Carcinoma
Author/Authors
Saitoh، نويسنده , , A. and Aoyagi، نويسنده , , Y. and Asakura، نويسنده , , H.، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 1993
Pages
7
From page
281
To page
287
Abstract
Chemical structures of the sugar chains of α1-antitrypsin (AAT) from patients with hepatocellular carcinoma (HCC) and from healthy individuals with a different affinity for Lens culinaris agglutinin (LCA) were examined by pyridylamination of their oligosaccharides and stepwise exoglycosidase digestion in combination with reversed-phase and size-fractionation high-performance liquid chromatography. We found that the LCA-reactive species of AAT from patients with HCC carried both the biantennary sugar chain with a fucose residue at the innermost N-acetylglucosamine residue, Galβ1-4GlcNAcβ1-2Manα1-6(Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4(Fucα1-6)GlcNAc-PA, and the biantennary chain without a fucose residue, Galβ1-4GlcNAcβ1-2Manα1-6(Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc-PA, at a ratio of about 1:0.6. The LCA-nonreactive species of AAT contained the biantennary sugar chain Galβ1-4GlcNAcβ1-2Manα1-6(Galβ1-4GlcNAcβ1-2Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAc as a major component. These results indicate that a characteristic feature of the carbohydrate chains of AAT from patients with HCC is an increment in fucosylation.
Journal title
Archives of Biochemistry and Biophysics
Serial Year
1993
Journal title
Archives of Biochemistry and Biophysics
Record number
1450432
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