Lipidomics by ultrahigh performance liquid chromatography-high resolution mass spectrometry and its application to complex biological samples

被引:89
|
作者
Triebl, Alexander [1 ]
Troetzmueller, Martin [1 ]
Hartler, Juergen [2 ]
Stojakovic, Tatjana [3 ]
Koefeler, Harald C. [1 ,4 ]
机构
[1] Med Univ Graz, Ctr Med Res, Core Facil Mass Spectrometry, Stiftingtalstr 24, A-8010 Graz, Austria
[2] Graz Univ Technol, Inst Computat Biotechnol, Petersgasse 14, A-8010 Graz, Austria
[3] Med Univ Graz, Clin Inst Med & Chem Lab Diagnost, Auenbruggetpl 15, A-8036 Graz, Austria
[4] Omics Ctr Graz, Stiftingtalstr 24, A-8010 Graz, Austria
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2017年 / 1053卷
基金
奥地利科学基金会;
关键词
High-resolution mass spectrometry; High performance liquid chromatography; Quantitative lipidomics; Lipid structural isomers; LINEAR DYNAMIC-RANGE; ELECTROSPRAY-IONIZATION; SHOTGUN LIPIDOMICS; HIGH-THROUGHPUT; HUMAN PLASMA; STRUCTURAL-CHARACTERIZATION; FRAGMENTATION PROCESSES; MOBILITY SPECTROMETRY; QUANTITATIVE-ANALYSIS; PHOSPHATE-COMPOUNDS;
D O I
10.1016/j.jchromb.2017.03.027
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An improved approach for selective and sensitive identification and quantitation of lipid molecular species using reversed phase chromatography coupled to high resolution mass spectrometry was developed. The method is applicable to a wide variety of biological matrices using a simple liquid-liquid extraction procedure. Together, this approach combines multiple selectivity criteria: Reversed phase chromatography separates lipids according to their acyl chain length and degree of unsaturation and is capable of resolving positional isomers of lysophospholipids, as well as structural isomers of diacyl phospholipids and glycerolipids. Orbitrap mass spectrometry delivers the elemental composition of both positive and negative ions with high mass accuracy. Finally, automatically generated tandem mass spectra provide structural insight into numerous glycerolipids, phospholipids, and sphingolipids within a single run. Calibration showed linearity ranges of more than four orders of magnitude, good values for accuracy and precision at biologically relevant concentration levels, and limits of quantitation of a few femtomoles on column. Hundreds of lipid molecular species were detected and quantified in three different biological matrices, which cover well the wide variety and complexity of various model organisms in lipidomic research. Together with a software package, this method is a prime choice for global lipidomic analysis of even the most complex biological samples. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:72 / 80
页数:9
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