State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Collaborative Innovation Center for Biotherapy, and Tianjin Key Laboratory of Molecular Drug Research, Nankai University, Tianjin, 300353, China.
Center for Diagnostics & Therapeutics and Department of Chemistry, Georgia State University, Atlanta, Georgia, 30303, USA.
Anal Bioanal Chem. 2017 Jan;409(2):421-429. doi: 10.1007/s00216-016-9690-x. Epub 2016 Jun 17.
Sensitive analysis of oligosaccharides by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) is significantly hampered by the low ionization efficiency of oligosaccharides. Derivatization affords a feasible way to enhance the MALDI intensities of oligosaccharides by introducing an easily ionized and/or hydrophobic tag to their reducing ends. However, tagging and subsequent desalting processes are quite time-consuming. Herein, we develop a rapid and sensitive approach for oligosaccharide derivatization by using 2-hydrazinopyrimidine (2-HPM). As a result of the presence of an electron-withdrawing N-heterocycle, 2-HPM can quantitatively derivatize oligosaccharides within 15 min and selectively facilitate their ionization. Additionally, 2-HPM acts as co-matrix to enhance the MALDI signal of oligosaccharides, and therefore the tedious enrichment and purification processes prior to MALDI analysis are avoided. This approach is applied to the analysis of various oligosaccharides released from glycopeptides, glycoprotein, and biological samples. After derivatization, a significant increase of MALDI intensities (greater than 10-fold) was observed for all the tested neutral and sialylated oligosaccharides. Moreover, the enhanced fragmentation of MS/MS brings much convenience to the structural elucidation of oligosaccharides. Graphical abstract Improved MALDI MS analysis of oligosaccharides by using 2-hydrazinopyrimidine as a derivative tag and co-matrix.
基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS)对寡糖的灵敏分析受到寡糖低离子化效率的严重阻碍。衍生化通过在寡糖的还原端引入易离子化和/或疏水性标记来提高 MALDI 强度,是一种可行的方法。然而,标记和随后的脱盐过程非常耗时。本文中,我们开发了一种使用 2- 肼基嘧啶(2-HPM)快速灵敏的寡糖衍生化方法。由于存在吸电子的 N-杂环,2-HPM 可以在 15 分钟内定量衍生化寡糖,并选择性地促进其离子化。此外,2-HPM 还可以作为共基质来增强寡糖的 MALDI 信号,从而避免了 MALDI 分析前繁琐的富集和纯化过程。该方法应用于从糖肽、糖蛋白和生物样品中释放的各种寡糖的分析。衍生化后,所有测试的中性和唾液酸化寡糖的 MALDI 强度均显著增加(大于 10 倍)。此外,MS/MS 的增强碎裂为寡糖的结构阐明带来了极大的便利。