Duteil S, Gareil P, Girault S, Mallet A, Feve C, Siret L
Laboratoire d'Electrochimie et Chimie Analytique, UMR CNRS 7575 - ENSCP, 75231 Paris cedex 05, France.
Rapid Commun Mass Spectrom. 1999;13(19):1889-98. doi: 10.1002/(SICI)1097-0231(19991015)13:19<1889::AID-RCM719>3.0.CO;2-#.
A direct coupling between capillary electrophoresis (CE) and ionspray (IS) mass spectrometry (MS) has been optimized to identify oligosaccharides obtained by enzymatic digestion of heparin. The separation electrolyte was made compatible with the requirements of a direct coupling using electrolytes made of ammonium acetate buffer, pH 3.5 and 9.2. The different parameters of the CE/IS interface were optimized using a standard mixture of disaccharides: flow rate and composition of the sheath liquid, flow rate of the sheath gas and position of the capillary in the needle. Different combinations of positive or negative CE voltage polarity and positive or negative MS ionization modes were investigated. They allowed for detection orders to be easily reversed and for complementary structural information to be gathered. Finally, the optimized methodology was applied to the separation and characterization of porcine mucosa heparin depolymerized by heparinases II and III.
毛细管电泳(CE)与离子喷雾(IS)质谱(MS)的直接联用已得到优化,用于鉴定肝素酶解所得的寡糖。使用pH值为3.5和9.2的醋酸铵缓冲液制成的电解质,使分离电解质符合直接联用的要求。利用二糖标准混合物优化了CE/IS接口的不同参数:鞘液的流速和组成、鞘气的流速以及毛细管在针中的位置。研究了正或负CE电压极性与正或负MS电离模式的不同组合。这些组合使得检测顺序易于反转,并能收集互补的结构信息。最后,将优化后的方法应用于肝素酶II和III解聚的猪黏膜肝素的分离与表征。