Heparin/heparan sulfate analysis by covalently modified reverse polarity capillary zone electrophoresis-mass spectrometry

被引:31
作者
Sanderson, Patience [1 ]
Stickney, Morgan [1 ]
Leach, Franklin E., III [1 ]
Xia, Qiangwei [2 ]
Yu, Yanlei [3 ]
Zhang, Fuming [3 ]
Linhardt, Roberti. [3 ]
Amster, I. Jonathan [1 ]
机构
[1] Univ Georgia, Dept Chem, Athens, GA 30602 USA
[2] CMP Sci Corp, 760 Parkside Ave,STE 211, Brooklyn, NY 11226 USA
[3] Rensselaer Polytech Inst, Biotech 4005,110 8th St, Troy, NY 12180 USA
基金
美国国家卫生研究院;
关键词
Capillary zone electrophoresis; Mass spectrometry; Sulfated glycosaminoglycan; Reverse polarity; Covalent capillary coating; Mixture analysis; ELECTRON DETACHMENT DISSOCIATION; HEPARAN-SULFATE; COMPOSITIONAL ANALYSIS; CHROMATOGRAPHY; GLYCOSAMINOGLYCANS; SEPARATION; COMPLEX; OLIGOSACCHARIDES; PHASE; IDENTIFICATION;
D O I
10.1016/j.chroma.2018.02.052
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Reverse polarity capillary zone electrophoresis coupled to negative ion mode mass spectrometry (CZEMS) is shown to be an effective and sensitive tool for the analysis of glycosaminoglycan mixtures. Covalent modification of the inner wall of the separation capillary with neutral or cationic reagents produces a stable and durable surface that provides reproducible separations. By combining CZE-MS with a cation coated capillary and a sheath flow interface, a rapid and reliable method has been developed for the analysis of sulfated oligosaccharides from dp4 to dp12. Several different mixtures have been separated and detected by mass spectrometry. The mixtures were selected to test the capability of this approach to resolve subtle differences in structure, such as sulfation position and epimeric variation of the uronic acid. The system was applied to a complex mixture of heparin/heparan sulfate oligosaccharides varying in chain length from dp3 to dp12 and more than 80 molecular compositions were identified by accurate mass measurement. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:75 / 83
页数:9
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