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Negative Matrix-Assisted Laser Desorption/Ionization Time-of-Flight/Time-of-Flight Tandem Mass Spectrometry Fragmentation of Synthetic Analogs of the O-Specific Polysaccharide of Vibrio Cholerae O:1 in the Presence of Anionic Dopants

Oligosaccharides (tri- to hexamers) that represent terminal epitopes of O-antigens of Vibrio cholerae O:1, serotypes Ogawa and Inaba, have been studied by negative matrix-assisted laser desorption/ionization time-of-flight/time-of-flight mass spectrometry (MALDI-ToF/ToF MS). The [M – H+]− ions are f...

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Bibliographic Details
Published in:European journal of mass spectrometry (Chichester, England) England), 2007-01, Vol.13 (5), p.347-353
Main Authors: Chmelík, Josef, Řehulka, Pavel, Kováčik, Vladimír, Pätoprstý, Vladimír, Kováč, Pavol
Format: Article
Language:English
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Summary:Oligosaccharides (tri- to hexamers) that represent terminal epitopes of O-antigens of Vibrio cholerae O:1, serotypes Ogawa and Inaba, have been studied by negative matrix-assisted laser desorption/ionization time-of-flight/time-of-flight mass spectrometry (MALDI-ToF/ToF MS). The [M – H+]− ions are formed after expulsion of a proton from molecules studied under MALDI/MS analysis conditions in the negative mode. Several ammonium salts (chloride, nitrate, hydrogencarbonate and hydrogensulfate) were used as additives to increase the formation of negative ions from saccharides. The most efficient was the addition of ammonium hydrogencarbonate, which increased the number of [M – H+]− ions more than six times. Between three fragmentation pathways, the new conjugated transfer of electrons within the second downstream unit of oligosaccharides was discovered. Production of these ions, which has not been observed in any other kinds of measurement, distinguishes substances belonging to Ogawa and Inaba serotypes. The negative MALDI-ToF/ToF mass spectra are simpler and, at the same time, more informative, as compared with positive and negative electrospray ionization ion trap as well as with positive MALDI-ToF/ToF analysis.
ISSN:1469-0667
1751-6838
DOI:10.1255/ejms.891