Structural characterization of oligosaccharides using MALDI-TOF/TOF tandem mass spectrometry

被引:172
作者
Mechref, Y
Novotny, MV
Krishnan, C
机构
[1] Indiana Univ, Dept Chem, Bloomington, IN 47405 USA
[2] Appl Biosyst Inc, Framingham, MA 01701 USA
关键词
D O I
10.1021/ac0341968
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Extensive cross-ring fragmentation ions, which are very informative of the linkages of the monosaccharide residues constituting these molecules, were readily observed in the MALDI-TOF/TOF/MS/MS spectra of oligosaccharides. These ions, in some cases, were more intense than the commonly observed Y and B ions. The A-type ions observed for the simple oligosaccharides allowed the distinction between alpha(1-4)- and alpha(1-6)-linked isobaric structures. The distinction was based not merely on the differences in the type of ions formed, but also on the ion intensities. For example, both alpha(1 -4)- and alpha(1-6)-linked isobaric structures produce ions resulting from the loss of similar to120 m/z units, but with different intensities, as a result of the fact that they correspond to two different ions (i.e., (0,4)A- and (2,4)A-ions), requiring different energies to be formed. Abundant A- and X-type ions were also observed for high-mannose N-glycans, allowing the determination of linkages. In addition, the high resolution furnished by MALDI-TOF/TOF allowed determination of certain ions that were commonly overlooked by MALDI-TOF or MALDI-magnetic sector instruments as a result of their lower resolution. Moreover, as a result of the fact that MS/MS spectra for parent ions and all fragment ions are acquired under the same experimental conditions, accurate determination of the molar ratios of isomeric glycans in a mixture analyzed simultaneously by MALDI-TOF/TOF tandem MS becomes possible.
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页码:4895 / 4903
页数:9
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