Department of Chemistry, Zhejiang University, Hangzhou, Zhejiang 310058, People's Republic of China.
Analysis Center of Agrobiology and Environmental Sciences, Zhejiang University, Hangzhou, Zhejiang 310058, People's Republic of China.
Anal Chem. 2024 Oct 15;96(41):16145-16153. doi: 10.1021/acs.analchem.4c02555. Epub 2024 Oct 3.
glycosylation is closely linked to a wide range of biological functions in organisms. Owing to the constriction of awful crystals formed by conventional MALDI matrices and the extremely inferior ionization efficiency of glycans, the traditional direct detection of glycans by matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) has been gradually replaced by postderivatization detection using reactive matrices. Nevertheless, the laborious identification of complex spectral peaks remains the major difficulty in glycan profiling. Hence, we logically designed and synthesized two novel reactive matrices, 2-nitro-4-carboxylphenylhydrazine (NCPH) and 2,4-dicarboxylphenylhydrazine (DCPH), and separately combined them with the acidic matrix 2,5-dihydroxybenzoic acid (DHB) to constitute two composite matrices with high on-target derivatization efficiency and significant promotion of glycan ionization for productive MALDI analysis in dual ion modes. Using both composite matrices, we can actualize MALDI-MS and MS mass calibration in dual ion modes by postderivatization detection and fragmentation of dextrans and selectively enhance the ionization effect of oligosaccharides in mixed systems. Quite homogeneous cocrystals can ensure glycan quantification with decent linearity and reproducibility. A fixed mass difference derived from the identical glycan in two ion modes is available for rapid identification in complex biological samples. Ultimately, the developed strategy was triumphantly employed to identify and quantify the relative content and alteration tendency of peach glycans, which can be referable to the latent correlation between glycan expression and peach ripening.
糖基化与生物体中广泛的生物功能密切相关。由于常规 MALDI 基质形成的可怕晶体的限制以及聚糖的电离效率极低,传统的基质辅助激光解吸/电离质谱(MALDI-MS)直接检测聚糖已逐渐被使用反应性基质的衍生化检测所取代。然而,复杂谱峰的费力鉴定仍然是糖谱分析的主要困难。因此,我们合理地设计和合成了两种新型反应性基质,2-硝基-4-羧基苯肼(NCPH)和 2,4-二羧基苯肼(DCPH),并分别将它们与酸性基质 2,5-二羟基苯甲酸(DHB)结合,构成了两种具有高靶标衍生化效率和显著促进聚糖离子化的复合基质,可用于双离子模式下的高效 MALDI 分析。使用这两种复合基质,我们可以通过衍生化检测和葡聚糖的碎裂,在双离子模式下实现 MALDI-MS 和 MS 质量校准,并选择性地增强混合体系中低聚糖的电离效果。非常均匀的共晶可确保聚糖定量具有良好的线性和重现性。两个离子模式中相同聚糖的固定质量差可用于快速鉴定复杂生物样品中的糖。最终,所开发的策略成功地用于鉴定和定量桃糖的相对含量和变化趋势,这可归因于糖表达与桃成熟之间的潜在相关性。