Zhang Fagen, Bartels Michael J, Stott William T
Toxicology and Environmental Research & Consulting, The Dow Chemical Company, 1803 Building, Midland, MI 48674, USA.
Rapid Commun Mass Spectrom. 2004;18(4):491-8. doi: 10.1002/rcm.1364.
Direct quantitation of glutathione S-transferase (GST) isoforms [alpha (GST-A) and micro (GST-M)] in human liver cytosol was achieved by liquid chromatography/tandem mass spectrometry (LC/ESI-MS/MS) analysis of signature peptides of GST-A and GST-M and their corresponding stable isotopic peptide internal standards via multiple reaction monitoring (MRM). The selection of signature peptides was performed via trypsin digestion of commercially available cDNA-expressed GST-A1 and GST-M1, followed by LC/ESI-MS/MS with an ion trap mass spectrometer and sequencing with the TurboSEQUEST application. Quantitative analysis of the selected signature peptides in the multi-reaction monitoring (MRM) mode was performed using a triple-quadruple mass spectrometer. A series of human cytosol samples was quantitatively analyzed for levels of GST-A and GST-M. The total level of GST-A and GST-M obtained from this LC/ESI-MS/MS method was well correlated with the total level of GST determined by the 1-chloro-2,4-dinitrobenzene (CDNB) method.
通过液相色谱/串联质谱(LC/ESI-MS/MS)对谷胱甘肽S-转移酶(GST)同工型[α(GST-A)和μ(GST-M)]的特征肽及其相应的稳定同位素肽内标进行多反应监测(MRM)分析,实现了对人肝细胞溶质中GST同工型的直接定量。特征肽的选择是通过对市售cDNA表达的GST-A1和GST-M1进行胰蛋白酶消化,然后用离子阱质谱仪进行LC/ESI-MS/MS分析,并使用TurboSEQUEST软件进行测序。使用三重四极杆质谱仪在多反应监测(MRM)模式下对选定的特征肽进行定量分析。对一系列人肝细胞溶质样品进行了GST-A和GST-M水平的定量分析。通过这种LC/ESI-MS/MS方法获得的GST-A和GST-M的总水平与通过1-氯-2,4-二硝基苯(CDNB)方法测定的GST总水平高度相关。