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首页> 外文期刊>Analytical and bioanalytical chemistry >The combination of 2,5-dihydroxybenzoic acid and 2,5-dihydroxyacetophenone matrices for unequivocal assignment of phosphatidylethanolamine species in complex mixtures
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The combination of 2,5-dihydroxybenzoic acid and 2,5-dihydroxyacetophenone matrices for unequivocal assignment of phosphatidylethanolamine species in complex mixtures

机译:2,5-二羟基苯甲酸和2,5-二羟基乙酮基质的组合用于复合混合物中磷脂酰乙醇胺种类的含量不确定分配

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Abstract Unequivocal assignment of phospholipid peaks in complex mixtures is difficult if only the m/z values but no tandem mass spectrometry (MS/MS) data are available. This is usually the case for matrix-assisted laser/desorption ionization time-of-flight (MALDI-TOF) MS imaging experiments and the analysis has normally to be performed without prior separation. Another problem might be the often matrix-induced loss of one methyl group in phosphatidylcholine (PC) species, which makes them detectable as negative ions becoming isomers of some phosphatidylethanolamines (PEs). Selected lipid mixtures of known compositions were investigated by negative ion MALDI-TOF MS and various imaging experiments. In addition to common matrices such as 2,5-dihydroxybenzoic acid (DHB) and 9-aminoacridine (9-AA), different binary matrices, including 2,5-dihydroxyacetophenone (2,5-DHAP) as matrix additive to DHB, were tested to probe their performance in both ionization modes. Beside artificial PC and PE mixtures of known compositions, egg yolk and liver extracts as well as cryosections from liver and pancreas tissue were selected as biologically relevant systems. The majority of the binary MALDI matrices used here leads to the loss of a methyl group from PC in the negative ion mode, which makes the clear identification of PE species ambiguous. However, this problem does not apply if a mixture of DHB and 2,5-DHAP is used. Therefore, the application of DHB/2,5-DHAP as matrix is a simple method to unequivocally identify PEs even in complex mixtures and tissue sections as negative ions and without the necessity to separate the individual lipid classes prior to MS detection. Graphical abstract Many common MALDI matrices (such as 9-AA) induce the loss of a methyl group from PC rendering the PC detectable as negative ion. These ions ( m/z 744.6 in the upper trace) represent isomers of typical PE species. It will be shown that this problem can be avoided if mixtures between DHB and 2,5-DHAP ar
机译:摘要如果只有M / Z值,但是没有串联质谱(MS / MS)数据,则难以使用复杂混合物中的磷脂峰的明确分配。这通常是矩阵辅助激光/解吸电离飞行时间(MALDI-TOF)MS成像实验的情况,并且通常在未经分离的情况下进行分析。另一个问题可能是磷脂酰胆碱(PC)物种中的一种甲基的常见损失,这使得它们可检测为阴离子成为一些磷脂酰乙醇胺(PES)的异构体。通过负离子MALDI-TOF MS和各种成像实验研究了已知组合物的所选脂质混合物。除了常见的基质之外,例如2,5-二羟基苯甲酸(DHB)和9-氨基丙氨酸(9-AA),包括2,5-二羟基乙酮(2,5-DHAP)作为DHB的基质添加剂的不同二元矩阵测试以探测其两种电离模式的性能。在人造PC和PE的已知组合物中,选择蛋黄和肝提取物以及来自肝脏和胰腺组织的冷冻液作为生物相关系统。这里使用的二元马尔迪基质的大部分MALDI基质导致来自负离子模式的PC的甲基损失,这使得PE物种的含糊不清的鉴定。但是,如果使用DHB和2,5-DHAP的混合物,则该问题不适用。因此,DHB / 2,5-DHAP作为基质的应用是一种简单的方法,即使在复杂的混合物和组织切片中毫不含糊地识别PES作为负离子,并且在没有必要之前在MS检测之前将个体脂质类分离。图形摘要许多常见的MALDI矩阵(例如9-AA)诱导来自PC的甲基损失,使PC可检测为负离子。这些离迹情况(上迹线中的m / z 744.6)代表典型体育物种的异构体。将显示,如果DHB和2,5-DHAP AR之间的混合物,则可以避免此问题

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