On-line sheathless capillary electrophoresis/nanoelectrospray ionization-tandem mass spectrometry for the analysis of glycosaminoglycan oligosaccharides

被引:75
作者
Zamfir, A
Seidler, DG
Schönherr, E
Kresse, H
Peter-Katalinic, J
机构
[1] Univ Munster, Biomed Anal Dept, Inst Med Phys & Biophys, D-48149 Munster, Germany
[2] Univ Munster, Inst Physiol Chem, D-48149 Munster, Germany
[3] Univ Munster, Inst Pathobiochem, D-48149 Munster, Germany
[4] Univ Wales Coll Cardiff, Coll Med, Sch Dent, Matrix Biol & Tissue Repair Res Unit, Cardiff, S Glam, Wales
关键词
capillary electrophoresis; electrospray ionization; glycosaminoglycans; mass spectrometry;
D O I
10.1002/elps.200405925
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A novel approach in glycosaminoglycomics, based on sheathless on-line capillary electrophoresis/nanoelectrospray ionization-quadrupole time of flight-mass spectrometry (CE/nanoESI-QTOF-MS) and tandem MS of extended chondroitin sulfate/dermatan (CS/DS) oligosaccharide chains is described. The methodology required the construction of a new sheathless CE/nanoESI-QTOF-MS configuration, its implementation and optimization for the high sensitivity analysis of CS/DS oligosaccharide mixtures from conditioned culture medium of decorin transfected human embryonic kidney (HEK) 293 cells. Under newly established sheathless on-line CE/(-)nanoESI conditions for glycosaminoglycan (GAG) ionization and MS detection, single CS/DS oligosaccharide components of extended chain length and increased sulfation degree were identified. Molecular ions corresponding to species carrying 5 and 6 negative charges could be generated for large GAG oligosaccharide species in the negative ion nanoESI-MS. The optimized on-line conditions enabled the detection of molecular ions assigned to oversulfated tetradeca-, octadeca-, and eicosasaccharide CS/DS molecules, which represent the category of largest sulfated GAG-derived oligosaccharides evidenced by CE/ESI-MS. By on-line CE/ESI tandem MS in data-dependent acquisition mode the oversulfated eicosasaccharide species could be sequenced and the localization of the additional sulfate group along the chain could be determined.
引用
收藏
页码:2010 / 2016
页数:7
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