Department of Chemistry, University of California, Davis, Davis, California 95616, United States.
Innovation Institute for Food and Health, University of California, Davis, Davis, California 95616, United States.
Anal Chem. 2024 Apr 16;96(15):5951-5959. doi: 10.1021/acs.analchem.4c00077. Epub 2024 Apr 2.
Sphingolipids are an essential subset of bioactive lipids found in most eukaryotic cells that contribute to membrane biophysical properties and are involved in cellular differentiation, recognition, and mediating interactions. The described nanoHPLC-ESI-Q/ToF methodology utilizes known biosynthetic pathways, accurate mass detection, optimized collision-induced disassociation, and a robust nanoflow chromatographic separation for the analysis of intact sphingolipids found in human tissue, cells, and serum. The methodology was developed and validated with an emphasis on addressing the common issues experienced in profiling these amphipathic lipids, which are part of the glycocalyx and lipidome. The high sensitivity obtained using nanorange flow rates with robust chromatographic reproducibility over a wide range of concentrations and injection volumes results in confident identifications for profiling these low-abundant biomolecules.
鞘脂类是大多数真核细胞中生物活性脂质的重要组成部分,有助于膜的生物物理特性,并参与细胞分化、识别和介导相互作用。所描述的纳升 HPLC-ESI-Q/ToF 方法利用已知的生物合成途径、精确质量检测、优化的碰撞诱导解离和稳健的纳流色谱分离,来分析人组织、细胞和血清中存在的完整鞘脂类。该方法是开发和验证的,重点是解决在分析这些亲脂性脂质(糖萼和脂类组的一部分)时遇到的常见问题。使用纳米级流速获得的高灵敏度和在广泛浓度和进样体积范围内具有稳健的色谱重现性,可确保对这些低丰度生物分子进行可靠的分析。