Structural Characterization of Fucose-Containing Oligosaccharides by High-Performance Liquid Chromatography and Matrix-Assisted Laser Desorption/ Ionization Time-of-Flight Mass Spectrometry
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Minoru Suzuki
Abstract
Eight pyridylamino (PA) derivatives of fucosecontaining oligosaccharides, which occur as free oligosaccharides in human milk and also are derived from glycosphingolipids, have been analyzed by highperformance liquid chromatography (HPLC) on normalphase and reversedphase columns, and by matrixassisted laser desorption/ionization timeofflight MALDITOF) mass spectrometry. Six out of eight PAoligosaccharides were clearly separated by both normal and reversedphase HPLC at a column temperature of 40 C, but two PAoligosaccharides, lactoNfucopentaose II [Gal?1-3(Fuc?1-4)GlcNAc?1- 3Gal?1-4GlcPA] and lactoNfucopentaose III Gal?1-4(Fuc?1-3)GlcNAc?1-3Gal?1-4GlcPA], were not separated. The two unresolved PAoligosaccharides were finally separated by reversedphase HPLC at a column temperature of 11 C. MALDITOF mass spectra of PAoligosaccharides demonstrated pseudomolecular ions as the predominant signals, therefore information about the molecular mass of each PAoligosaccharide was easily obtained. Postsource decay (PSD) MALDITOF mass spectra of PAoligosaccharides gave information about the carbohydrate sequences and carbohydrate species of each PAoligosaccharide by detecting the ions responsible for the cleavage of the glycosidic bonds. The detection limits of the PAoligosaccharides by HPLC, MALDITOF mass spectrometry, and PSD MALDITOF mass spectrometry were 20 fmol, 20 fmol, and 2 pmol, respectively. These results suggest that a system including HPLC and MALDITOF mass spectrometry or HPLC and PSD MALDITOF mass spectrometry is quite useful for the structural characterization of subpmol or pmol levels of fucosecontaining oligosaccharides, and that these methods could be used for the analysis of various types of oligosaccharides derived from glycoproteins and glycosphingolipids.
Copyright © 2001 by Walter de Gruyter GmbH & Co. KG
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Artikel in diesem Heft
- Highlight: Glycobiology
- O-Glycosylation of the Mucin Type
- Glycoproteins from Insect Cells: Sialylated or Not?
- Congenital Disorders of Glycosylation: Glycosylation Defects in Man and Biological Models for Their Study
- Mitochondrial Single-Stranded DNA-Binding Proteins: in Search for New Functions
- Do Rodent and Human Brains Have Different N-Glycosylation Patterns?
- The Liver Flukes Fasciola gigantica and Fasciola hepatica Express the Leucocyte Cluster of Differentiation Marker CD77 (Globotriaosylceramide) in Their Tegument
- Cloning and Expression of Drosophila melanogaster UDP-GlcNAc:?-3-D-Mannoside ? 1,2-N-Acetylglucosaminyltransferase I
- Pathways of Mucin O-Glycosylation in Normal and Malignant Rat Colonic Epithelial Cells Reveal a Mechanism for Cancer-Associated Sialyl-Tn Antigen Expression
- 6-O-Sulfo De-N-Acetylsialyl Lewis X as a Novel High-Affinity Ligand for Human L-Selectin: Total Synthesis and Structural Characterization
- Segregation of Gangliosides GM1 and GD3 on Cell Membranes, Isolated Membrane Rafts, and Defined Supported Lipid Monolayers
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- Anencephaly: Structural Characterization of Gangliosides in Defined Brain Regions
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- Experimental Regulation of STAT Gene Expression Reveals an Involvement of STAT5 in Interleukin-4-Driven Cell Proliferation
