Characterization by gas-liquid chromatography-mass spectrometry of oligosaccharides resulting from the hydrazinolysis-nitrous acid deamination reaction of glycopeptides
✍ Scribed by Gérard Strecker; Annick Pierce-Cretel; Bernard Fournet; Geneviève Spik; Jean Montreuil
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- English
- Weight
- 532 KB
- Volume
- 111
- Category
- Article
- ISSN
- 0003-2697
No coin nor oath required. For personal study only.
✦ Synopsis
The hydrazinolysis-nitrous acid deamination of glycopeptides leads to the specific cleavage of N-acetylglucosamine linkages. The 2,5-anhydro-mannose containing oligosaccharides obtained by this way are reduced by sodium borohydride, methylated, and analyzed by gas-liquid chromatography-mass spectrometry. Here we report the characterization of 11 oligosaccharides obtained from various fucosyl-glycoasparagines and glycopeptides. In addition, the structure of a partially characterized glycopeptide isolated from human milk sIgA was investigated as an application of the present method.
📜 SIMILAR VOLUMES
The structural features of humic acids (HAs) isolated from sediments on the bottom of dam reservoirs that can affect their binding capacities for Fe(II) were investigated by pyrolysis-gas chromatography/mass spectroscopy using tetramethylammonium hydroxide (TMAH-py-GC/MS). The binding capacities for