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用高灵敏度毛细管电泳-质谱法对来源于中性糖脂的吡啶基氨化寡糖进行结构表征。

Structural characterization of pyridylaminated oligosaccharides derived from neutral glycosphingolipids by high-sensitivity capillary electrophoresis-mass spectrometry.

机构信息

Systems Glycobiology Research Group, RIKEN-Max Planck Joint Research Center, Global Research Cluster, RIKEN, Wako-shi, Saitama, Japan.

出版信息

Anal Chem. 2013 Aug 20;85(16):7859-65. doi: 10.1021/ac401460f. Epub 2013 Aug 9.

Abstract

High-sensitivity capillary electrophoresis-electrospray ionization quadrupole ion trap time-of-flight mass spectrometry (CE-ESI-QIT-TOF MS) was developed to structurally characterize four kinds of pyridylaminated (PA) oligosaccharides, i.e., lactose (Lac)-PA, globotriose (Gb3)-PA, globotetraose (Gb4)-PA, and IV(3) αGalNAc-Gb4 (Forssman antigen)-PA, derived from neutral glycosphingolipids. The CE-MS system included the head-column field-amplified sample stacking (HC-FASS) method for effective sample injection into a capillary column in CE, a sheathless interface between CE and a mass spectrometer, and MS and tandem MS (MS(2)) measurements with narrow mass range repeated high-speed switching. The total sensitivity of the developed CE-MS system was about 20,000 times higher than that of the conventional CE-MS system consisting of pressure injection, a sheath-flow interface, and a wide mass range measurement. The MS and MS(2) spectra of the four PA-oligosaccharides at a concentration of 25 amol/μL in mixtures (each 250 amol/10 μL in a tube) clearly showed protonated molecular ions (M + H) and the fragment ions responsible for the sequential elimination of saccharides. The developed CE-MS system is a powerful method for the structural characterization of glycosphingolipids extracted from very small amounts of biological materials and could be extended to the structural characterization of oligosaccharides derived from glycoproteins.

摘要

高灵敏度毛细管电泳-电喷雾电离四极杆离子阱飞行时间质谱(CE-ESI-QIT-TOF MS)被开发用于结构表征四种吡啶基胺化(PA)寡糖,即乳糖(Lac)-PA、神经节苷脂 Gb3(Gb3)-PA、神经节苷脂 Gb4(Gb4)-PA 和 IV(3)αGalNAc-Gb4(福斯曼抗原)-PA,它们来源于中性糖脂。CE-MS 系统包括用于在 CE 中有效将样品注入毛细管柱的柱顶场放大样品堆积(HC-FASS)方法、CE 与质谱仪之间的无鞘接口以及具有窄质量范围的重复高速切换的 MS 和串联 MS(MS(2)) 测量。与由压力进样、鞘流接口和宽质量范围测量组成的传统 CE-MS 系统相比,开发的 CE-MS 系统的总灵敏度大约提高了 20,000 倍。在混合物中浓度为 25 amol/μL 的四种 PA-寡糖的 MS 和 MS(2)谱(每个管中 250 amol/10 μL)清楚地显示了质子化分子离子(M + H)和负责糖依次消除的碎片离子。开发的 CE-MS 系统是一种从非常少量生物材料中提取的糖脂进行结构表征的强大方法,并且可以扩展到糖蛋白衍生的寡糖的结构表征。

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