Summary
Disaccharide fragments resulting from the enzymatic digestion of heparins with heparinase have been purified by gel filtration chromatography and directly analyzed by positive and negative ion liquid secondary ion mass spectrometry (LSIMS). Following the chromatographic purification from excess sodium salt, the mass spectra of di- and tetrasaccharide fragment mixtures enabled the identification of up to three covalently bound sulfate moieties per glycosaminoglycan-disaccharide unit, by means of their molecular ions, containing the corresponding alkali-counterions.
Similar content being viewed by others
References
Ehrlich J, Stivala SS (1973) J Pharm Sci 62:517
Linker A, Hovingh P (1972) Biochemistry 11:563
Linhardt RJ, Fitzgerald GL, Cooney CL, Langer R (1982) Biochim Biophys Acta 702:2029
Carr SA, Reinhold VN (1984) J Carbohydr Chem 3:381
Abert W, Straub KM, Burlingame AL (1982) Anal Chem 54:2029
Przyblyski M (1987) In: Krebsforschung 1980–1987; BMFT-Rep. 379–437
Reinhold VN, Carr SA, Green BN, Petitou M, Choay J, Sinay P (1987) Carbohydr Res 161:305
Przybylski M (1983) Fresenius Z Anal Chem 315:402
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Brandau, B.E., Fonrobert, P., Przybylski, M. et al. Characterisation of disaccharide fragments from the enzymatic digestion of heparin by liquid secondary ion mass spectrometry. Z. Anal. Chem. 331, 55–57 (1988). https://doi.org/10.1007/BF00473897
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00473897