Luo Bing, Groenke Karsten, Takors Ralf, Wandrey Christian, Oldiges Marco
Institute of Biotechnology, Research Centre Juelich GmbH, D-52425 Jülich, Germany.
J Chromatogr A. 2007 Apr 20;1147(2):153-64. doi: 10.1016/j.chroma.2007.02.034. Epub 2007 Feb 16.
A highly selective and sensitive method for identification and quantification of intracellular metabolites involved in central carbon metabolism (including glycolysis, pentose phosphate pathway and tricarboxylic acid cycle) by means of liquid chromatography-tandem quadrupole mass spectrometry (LC-MS/MS) was developed. The volatile ion pair modifier tributylammonium acetate (TBAA) was employed in the mobile phase for simultaneously separation of 29 negatively charged compounds including sugar phosphates, nucleotides, and carboxylic acids on a common C18 reversed-phase column. Method validation results displayed that limits of detection (LODs) calculated according to DIN (German Institute for Standardization) 32645 are mostly below 60 nM, only with the exception of pyruvate and malate. The calibration curves showed excellent linearity mainly over three orders of magnitude with correlation coefficients R(2)>0.9982. This LC-MS/MS method was successfully applied to determine these metabolites in cell extracts of Escherichia coli. Most of the intracellular metabolites were found within the detection range and the relative standard deviations of the measurements were smaller than 5.65% (n=5) for a cell extract sample.
开发了一种高选择性和灵敏的方法,通过液相色谱 - 串联四极杆质谱(LC-MS/MS)来鉴定和定量参与中心碳代谢(包括糖酵解、磷酸戊糖途径和三羧酸循环)的细胞内代谢物。在流动相中使用挥发性离子对改性剂乙酸三丁铵(TBAA),以便在普通的C18反相柱上同时分离29种带负电荷的化合物,包括磷酸糖、核苷酸和羧酸。方法验证结果表明,根据德国标准化协会(DIN)32645计算的检测限(LOD)大多低于60 nM,只有丙酮酸和苹果酸除外。校准曲线主要在三个数量级上显示出优异的线性,相关系数R(2)>0.9982。这种LC-MS/MS方法成功应用于测定大肠杆菌细胞提取物中的这些代谢物。大多数细胞内代谢物都在检测范围内,对于细胞提取物样品,测量的相对标准偏差小于5.65%(n = 5)。