Hořejší Karel, Jirásko Robert, Chocholoušková Michaela, Wolrab Denise, Kahoun David, Holčapek Michal
Department of Analytical Chemistry, Faculty of Chemical Technology, University of Pardubice, Studentská 573, 532 10 Pardubice, Czech Republic.
Institute of Chemistry, Faculty of Science, University of South Bohemia in České Budějovice, Branišovská 1760, 370 05 České Budějovice, Czech Republic.
Metabolites. 2021 Feb 26;11(3):140. doi: 10.3390/metabo11030140.
Glycosphingolipids (GSL) represent a highly heterogeneous class of lipids with many cellular functions, implicated in a wide spectrum of human diseases. Their isolation, detection, and comprehensive structural analysis is a challenging task due to the structural diversity of GSL molecules. In this work, GSL subclasses are isolated from human plasma using an optimized monophasic ethanol-water solvent system capable to recover a broad range of GSL species. Obtained deproteinized plasma is subsequently purified and concentrated by C18-based solid-phase extraction (SPE). The hydrophilic interaction liquid chromatography coupled to electrospray ionization linear ion trap tandem mass spectrometry (HILIC-ESI-LIT-MS/MS) is used for GSL analysis in the human plasma extract. Our results provide an in-depth profiling and structural characterization of glycosphingolipid and some phospholipid subclasses identified in the human plasma based on their retention times and the interpretation of tandem mass spectra. The structural composition of particular lipid species is readily characterized based on the detailed interpretation of mass spectrometry (MS) and tandem mass spectrometry (MS/MS) spectra and further confirmed by specific fragmentation behavior following predictable patterns, which yields to the unambiguous identification of 154 GSL species within 7 lipid subclasses and 77 phospholipids representing the highest number of GSL species ever reported in the human plasma. The developed HILIC-ESI-MS/MS method can be used for further clinical and biological research of GSL in the human blood or other biological samples.
糖鞘脂(GSL)是一类高度异质的脂质,具有多种细胞功能,与多种人类疾病有关。由于GSL分子的结构多样性,其分离、检测和全面的结构分析是一项具有挑战性的任务。在这项工作中,使用优化的单相乙醇 - 水溶剂系统从人血浆中分离GSL亚类,该系统能够回收广泛的GSL种类。随后,通过基于C18的固相萃取(SPE)对获得的脱蛋白血浆进行纯化和浓缩。亲水相互作用液相色谱与电喷雾电离线性离子阱串联质谱联用(HILIC - ESI - LIT - MS/MS)用于人血浆提取物中的GSL分析。我们的结果基于其保留时间和串联质谱的解释,对人血浆中鉴定出的糖鞘脂和一些磷脂亚类进行了深入的剖析和结构表征。根据质谱(MS)和串联质谱(MS/MS)谱的详细解释,可以很容易地确定特定脂质种类的结构组成,并通过遵循可预测模式的特定碎片行为进一步确认,这使得在7个脂质亚类中明确鉴定出154种GSL种类和77种磷脂,这是人类血浆中报道的GSL种类数量最多的。所开发的HILIC - ESI - MS/MS方法可用于人血液或其他生物样品中GSL的进一步临床和生物学研究。