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Automated normal phase nano high performance liquid chromatography/matrix assisted laser desorption/ionization mass spectrometry for analysis of neutral and acidic glycosphingolipids

机译:自动化正相纳米高效液相色谱/基质辅助激光解吸/电离质谱分析中性和酸性糖鞘脂

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The coupling of nano high-performance liquid chromatography (nanoHPLC) with matrix-assisted laser desorption/ionization (MALDI) mass spectrometry (MS) via an automatic spotting roboter was developed and adapted for the first time for the analysis of complex mixtures of glycosphingolipids (GSLs). The 2,5-dihydroxybenzoic acid and 6-azo-2-thiothymine matrix systems were adjusted to concurrently meet the requirements for reproducible and homogeneous crystal formation with the liquid chromatography (LC) eluent under the variable LC solvent composition over the course gradient and high ionization efficiency of the GSL species, without the need for recrystallization. Precise adjustment of the automatic spotting parameters in terms of matrix flow rate, on-tip collection time of the matrix/LC eluent solution and the matrix spotting mode, i.e., continuous and discontinuous, was accomplished to collect individually nanoHPLC-separated species within distinct spots and consequently recover by MALDI MS screening all major and minor GSL species in the mixtures. The nanoHPLC/MALDI MS coupling protocol was developed and applied to a mixture of neutral GSLs purified from human erythrocytes and a monosialoganglioside mixture expressed by the murine MDAY-D2 cell line. Additionally, on-line nanoHPLC/MALDI doping with lithium cations of individually separated neutral GSLs was introduced to enhance data interpretation of the GSL MS pattern, while preserving the same level of information and ultimately to enhance structural assignment of components of interest. The method is demonstrated to be highly sensitive, reaching the low femtomole level of detection of individual GSL species and is highlighted as a versatile analytical tool for glycolipidomic studies.
机译:通过自动点样机器人开发了纳米高效液相色谱(nanoHPLC)与基质辅助激光解吸/电离(MALDI)质谱(MS)的结合,并首次将其用于分析糖鞘脂的复杂混合物( GSL)。调整了2,5-二羟基苯甲酸和6-偶氮-2-硫代胸腺嘧啶基质体系,以同时满足液相色谱(LC)洗脱液在可变的LC溶剂组成下在整个过程梯度和高梯度下可重现和均匀形成晶体的要求GSL物质的电离效率,无需重结晶。根据基质流速,基质/ LC洗脱液的现场收集时间以及基质点样模式(即连续和不连续),对自动点样参数进行了精确调整,从而可以将纳米HPLC分离的物种分别收集到不同的点中然后通过MALDI MS筛选混合物中所有主要和次要GSL物种进行回收。开发了nanoHPLC / MALDI MS偶联方案并将其应用于从人红细胞纯化的中性GSL混合物和鼠MDAY-D2细胞系表达的单唾液酸神经节苷脂混合物。此外,引入了用单独分离的中性GSL的锂阳离子进行的在线nanoHPLC / MALDI掺杂,以增强GSL MS模式的数据解释,同时保留相同水平的信息,并最终增强目标组分的结构分配。该方法被证明是高度灵敏的,达到了检测单个GSL物种的低飞摩尔水平,并被强调为糖脂研究的通用分析工具。

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