Targeted Phosphoinositides Analysis Using High-Performance Ion Chromatography-Coupled Selected Reaction Monitoring Mass Spectrometry

被引:11
|
作者
Cheung, Hilaire Yam Fung [1 ,2 ,3 ]
Coman, Cristina [1 ,4 ]
Westhoff, Philipp [1 ]
Manke, Mailin [5 ]
Sickmann, Albert [1 ]
Borst, Oliver [5 ]
Gawaz, Meinrad [5 ]
Watson, Steve P. [2 ]
Heemskerk, Johan W. M. [3 ]
Ahrends, Robert [1 ,4 ]
机构
[1] Leibniz Inst Analyt Wissensch ISAS eV, D-44227 Dortmund, Germany
[2] Univ Birmingham, Inst Cardiovasc Sci, Inst Biomed Res, Coll Med & Dent Sci, Birmingham B15 2TT, W Midlands, England
[3] Maastricht Univ, Cardiovasc Res Inst Maastricht CARIM, Dept Biochem, NL-6229 ER Maastricht, Netherlands
[4] Univ Vienna, Dept Analyt Chem, Fac Chem, A-1090 Vienna, Austria
[5] Univ Tubingen, Dept Cardiol & Cardiovasc Med, D-72076 Tubingen, Germany
关键词
phosphoinositides; targeted lipidomics; ion chromatography; NECK-CANCER CELLS; RAT-BRAIN; INSULIN; QUANTIFICATION; LIPIDS; METABOLITES; 3-KINASE; HEAD;
D O I
10.1021/acs.jproteome.1c00017
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Phosphoinositides are minor components of cell membranes, but play crucial roles in numerous signal transduction pathways. To obtain quantitative measures of phosphoinositides, sensitive, accurate, and comprehensive methods are needed. Here, we present a quantitative targeted ion chromatography-mass spectrometry-based workflow that separates phosphoinositide isomers and increases the quantitative accuracy of measured phosphoinositides. Besides testing different analytical characteristics such as extraction and separation efficiency, the reproducibility of the developed workflow was also investigated. The workflow was verified in resting and stimulated human platelets, fat cells, and rat hippocampal brain tissue, where the LOD and LOQ for phosphoinositides were at 312.5 and 625 fmol, respectively. The robustness of the workflow is shown with different applications that confirms its suitability to analyze multiple less-abundant phosphoinositides.
引用
收藏
页码:3114 / 3123
页数:10
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