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Theβ-subunit of human chorionic gonadotropin containsN-glycosidic trisialo tri- and tri′-antennary carbohydrate chains
Authors:Jan B L Damm  Hans Voshol  Karl Hård  Johannis P Kamerling  Gijs W K Van Dedem  Johannes F G Vliegenthart
Institution:(1) Department of Bio-Organic Chemistry, Utrecht University, Transitorium III, P.O. Box 80.075, NL-3508 TB Utrecht, The Netherlands;(2) Diosynth B.V., P.O. Box 20, NL-5340 BH Oss, The Netherlands
Abstract:TheN-linked carbohydrate chains of thebeta-subunit of highly purified urinary human chorionic gonadotropin have been re-investigated. The oligosaccharides were released enzymatically by peptide-N 4-(N-acetyl-beta-glucosaminyl)asparagine amidase-F, and fractionated by a combination of FPLC and HPLC. As a result of the application of improved fractionation methods, apart from the earlier reported carbohydrate chains, also small amounts of trisialo tri- and triprime-antennary oligosaccharides were found. The primary structures of the latter carbohydrate chains have been determined by 500-MHz1H-NMR spectroscopy to beAbbreviations hCG human chorionic gonadotropin - hCG-beta beta-subunit - hCG-agr agr-subunit - PNGase-F peptide-N 4-(N-acetyl-beta-glucosaminyl)asparagine amidase-F (E.C. 3.5.1.52) - endo-F endo-beta-N-acetylglucosaminidase-F (E.C. 3.2.1.96) - SDS sodium dodecyl sulphate - PAGE polyacrylamide gel electrophoresis - CBB coomassie brilliant blue R 250 - GlcNAc N-acetylglucosamine - NeuAc N-acetylneuraminic acid - Man mannose - Gal galactose - Fuc fucose
Keywords:hCG  PNGase-F  FPLC  HPLC  1 H-NMR
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