A Targeted, Bioinert LC-MS/MS Method for Sensitive, Comprehensive Analysis of Signaling Lipids

被引:1
|
作者
Rubenzucker, Stefanie [1 ,2 ]
Manke, Mailin-Christin [3 ,4 ]
Lehmann, Rainer [5 ]
Assinger, Alice [6 ]
Borst, Oliver [3 ,4 ]
Ahrends, Robert [1 ]
机构
[1] Univ Vienna, Dept Analyt Chem, A-1090 Vienna, Austria
[2] Univ Vienna, Vienna Doctoral Sch Chem, A-1090 Vienna, Austria
[3] Univ Tubingen, DFG Heisenberg Grp Cardiovasc Thromboinflammat & T, D-72076 Tubingen, Germany
[4] Univ Tubingen, Dept Cardiol & Angiol, D-72076 Tubingen, Germany
[5] Univ Hosp Tubingen, Inst Clin Chem & Pathobiochem, Dept Diagnost Lab Med, D-72076 Tubingen, Germany
[6] Med Univ Vienna, Ctr Physiol & Pharmacol, Dept Vasc Biol & Thrombosis Res, A-1090 Vienna, Austria
基金
奥地利科学基金会;
关键词
SPHINGOSINE; 1-PHOSPHATE; LYSOPHOSPHATIDIC ACID; PLATELET; SPHINGOSINE-1-PHOSPHATE; QUANTIFICATION; REGULATOR; PLASMA; SERUM;
D O I
10.1021/acs.analchem.4c01388
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Signaling lipids are key players in cellular processes. Despite their importance, no method currently allows their comprehensive monitoring in one analytical run. Challenges include a wide dynamic range, isomeric and isobaric species, and unwanted interaction along the separation path. Herein, we present a sensitive and robust targeted liquid chromatography-mass spectrometry (LC-MS/MS) approach to overcome these challenges, covering a broad panel of 17 different signaling lipid classes. It involves a simple one-phase sample extraction and lipid analysis using bioinert reversed-phase liquid chromatography coupled to targeted mass spectrometry. The workflow shows excellent sensitivity and repeatability in different biological matrices, enabling the sensitive and robust monitoring of 388 lipids in a single run of only 20 min. To benchmark our workflow, we characterized the human plasma signaling lipidome, quantifying 307 endogenous molecular lipid species. Furthermore, we investigated the signaling lipidome during platelet activation, identifying numerous regulations along important lipid signaling pathways. This highlights the potential of the presented method to investigate signaling lipids in complex biological systems, enabling unprecedentedly comprehensive analysis and direct insight into signaling pathways.
引用
收藏
页码:9643 / 9652
页数:10
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