Mass Spectrometry of Glycosides


High-resolution mass spectrometry has become another valuable tool for characterization of simple and complex glycosides. The method is based on the collision of a high-energy electron against a sample under study producing as result a cation radical fragment known as the molecular ion, which should match with the molecular weight of the molecule. The mass spectrum also registers a number of fragments being the most intense the base peak assigned a relative intensity of 100. Mass spectrometry can be applied as high and low ionization experiments, being for the former the most suitable for glycosides electron impact and for the latter fast atom bombardment (FAB) and electrospray ionization the routine experiments for characterization of glycosides. In terms of sensitivity of the measurement this instrumental method requires small amount of sample, even in the order of nanogram quantities.


Fast Atom Bombardment Collisional Activation Fast Atom Bombardment Mass Spectrum Soft Ionization Method HexNAc Residue 
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  1. 1.
    K. Bieman, J. Am. Chem. Soc. 85, 2289 (1963).CrossRefGoogle Scholar
  2. 2.
    M. Brito-Arias, unpublished results.Google Scholar
  3. 3.
    K. Harada, M. Suzuki, and H. Kambara, Org. Mass. Spectrom, 1982, 17, 386.CrossRefGoogle Scholar
  4. 4.
    M. Dell, Advances in Carbohydrate Chemistry and Biochemistry, 1987, 45, 19.Google Scholar
  5. 5.
    J.-L. Wolfender, M. Maillard, A. Marston, and K., Hostettman, Pytochemical Analysis, 1992, 3, 193.CrossRefGoogle Scholar
  6. 6.
    M.A. Brito-Arias, R. Pereda-Miranda, and C.H. Heathcock, J. Org. Chem., 2004.Google Scholar
  7. 7.
    Morris, et al., J. Biol. Chem. 1978, 253, 5155.Google Scholar
  8. 8.
    A. Dell and H.R. Morris, Science, 2001, 291, 2351.CrossRefGoogle Scholar
  9. 9.
    Teng-umnuay et al., J. Biol. Chem. 1998, 273, 18242.CrossRefGoogle Scholar
  10. 10.
    A. Dell, Adv. Carbohydr. Chem. Biochem. 1987, 45, 19.CrossRefGoogle Scholar
  11. 11.
    R.L. Easton, M.S. Patankar, G.F. Clark, H.R. Morris, and A. Dell, J. Biol. Chem. 2000, 275, 21928.CrossRefGoogle Scholar

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