A reversed-phase capillary ultra-performance liquid chromatography-mass spectrometry (UPLC-MS) method for comprehensive top-down/bottom-up lipid profiling

被引:82
作者
Gao, Xiaoli [1 ]
Zhang, Qibin [1 ]
Meng, Da [1 ]
Isaac, Giorgis [1 ]
Zhao, Rui [2 ]
Fillmore, Thomas L. [2 ]
Chu, Rosey K. [2 ]
Zhou, Jianying [1 ]
Tang, Keqi [1 ]
Hu, Zeping [1 ]
Moore, Ronald J. [1 ]
Smith, Richard D. [1 ]
Katze, Michael G. [3 ,4 ]
Metz, Thomas O. [1 ]
机构
[1] Pacific NW Natl Lab, Div Biol Sci, Richland, WA 99352 USA
[2] Pacific NW Natl Lab, Environm Mol Sci Lab, Richland, WA 99352 USA
[3] Univ Washington, Sch Med, Dept Microbiol, Seattle, WA 98195 USA
[4] Univ Washington, Washington Natl Primate Res Ctr, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
Ultra-performance liquid chromatography (UPLC); Tandem mass spectrometry (MS/MS); Electrospray ionization (ESI); Top-down/bottom-up lipid profiling; HUMAN PLASMA PROTEOME; NANOELECTROSPRAY IONIZATION; QUANTITATIVE-ANALYSIS; SHOTGUN LIPIDOMICS; DYNAMIC-RANGE; ACCURATE MASS; BLOOD-PLASMA; ELECTROSPRAY; IDENTIFICATION; PHOSPHOLIPIDS;
D O I
10.1007/s00216-012-5773-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Lipidomics is a critical part of metabolomics and aims to study all the lipids within a living system. We present here the development and evaluation of a sensitive capillary UPLC-MS method for comprehensive top-down/bottom-up lipid profiling. Three different stationary phases were evaluated in terms of peak capacity, linearity, reproducibility, and limit of quantification (LOQ) using a mixture of lipid standards representative of the lipidome. The relative standard deviations of the retention times and peak abundances of the lipid standards were 0.29% and 7.7%, respectively, when using the optimized method. The linearity was acceptable at > 0.99 over 3 orders of magnitude, and the LOQs were sub-fmol. To demonstrate the performance of the method in the analysis of complex samples, we analyzed lipids extracted from a human cell line, rat plasma, and a model human skin tissue, identifying 446, 444, and 370 unique lipids, respectively. Overall, the method provided either higher coverage of the lipidome, greater measurement sensitivity, or both, when compared to other approaches of global, untargeted lipid profiling based on chromatography coupled with MS.
引用
收藏
页码:2923 / 2933
页数:11
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