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三羧酸循环中间产物的衍生化及在线固相萃取-液相色谱-质谱联用正离子电喷雾电离分析。

Derivatization of the tricarboxylic acid cycle intermediates and analysis by online solid-phase extraction-liquid chromatography-mass spectrometry with positive-ion electrospray ionization.

机构信息

VU University Amsterdam, Faculty of Sciences, BioMolecular Analysis Group, De Boelelaan 1083, 1081 HV Amsterdam, The Netherlands.

出版信息

J Chromatogr A. 2012 Apr 6;1232:19-26. doi: 10.1016/j.chroma.2011.07.095. Epub 2011 Aug 6.

Abstract

The analysis of cellular metabolic processes is of fundamental biological interest. Cellular metabolites, such as the intermediates of the tricarboxylic acid (TCA) cycle, provide essential information about the metabolic state of the cell. Not only is the TCA cycle a key factor in the energy regulation within aerobic cells, it possibly also plays a role in cell signaling. This paper describes a novel derivatization strategy, using the empirically selected N-methyl-2-phenylethanamine as derivatization reagent with a carbodiimide as co-reagent, for the selective derivatization of carboxylic acids, such as the di- and tri-carboxylic acids of the TCA cycle. Optimization of the derivatization protocol is described. This procedure enables analysis of the derivatives using on-line solid-phase extraction and reversed-phase liquid chromatography in combination with sensitive positive-ion electrospray ionization mass spectrometry. The complete procedure, involving the use of core-shell silica column material, allows the rapid analysis of TCA cycle intermediates in sample matrices, here shown for pig heart tissue extracts, with a good linearity over 3-4 orders of magnitude. Detection limits range from 12 to 1000 nM, depending on the analyte.

摘要

细胞代谢过程的分析具有重要的生物学意义。细胞代谢物,如三羧酸 (TCA) 循环的中间产物,为细胞的代谢状态提供了重要信息。TCA 循环不仅是有氧细胞能量调节的关键因素,它还可能在细胞信号转导中发挥作用。本文描述了一种新颖的衍生化策略,使用经验选择的 N-甲基-2-苯乙胺作为衍生化试剂,与碳二亚胺作为共试剂,用于选择性衍生化羧酸,如 TCA 循环的二羧酸和三羧酸。描述了衍生化方案的优化。该方法可使用在线固相萃取和反相液相色谱与灵敏的正离子电喷雾电离质谱联用对衍生物进行分析。该方法涉及使用核壳硅胶柱材料,可快速分析样品基质中的 TCA 循环中间产物,这里以猪心组织提取物为例,在 3-4 个数量级范围内具有良好的线性关系。检测限取决于分析物,范围为 12 至 1000 nM。

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