Toward fingerprinting cellular lipidomes directly from biological samples by two-dimensional electrospray ionization mass spectrometry

被引:164
作者
Han, XL [1 ]
Yang, JY
Cheng, H
Ye, HP
Gross, RW
机构
[1] Washington Univ, Sch Med, Div Bioorgan Chem & Mol Pharmacol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
[4] Washington Univ, Dept Chem, St Louis, MO 63130 USA
[5] US FDA, St Louis, MO 63101 USA
关键词
electrospray ionization mass spectrometry; lipidome; lipidomics; two-dimensional mass spectrometry;
D O I
10.1016/j.ab.2004.04.004
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cellular lipids are composed of linear combinations of aliphatic chains covalently attached to backbones and/or head groups that collectively represent the cellular lipidome. Herein we present a novel two-dimensional electrospray ionization mass spectrometric approach to fingerprint most of the major and many of the minor lipid classes in the hepatic cellular lipidome, which collectively represent > 80% of the total lipid mass, directly from their chloroform extracts. Through lipid class-selective intrasource ionization and subsequent analysis of two-dimensional cross-peak intensities, the chemical identity and mass composition of individual molecular species of most mouse hepatic lipid classes were determined from its chloroform extract. This new integrated platform provides a robust foundation for the automated analysis of multidimensional mass spectra to advance the level of analytical scripting in lipidomics to a new plateau. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:317 / 331
页数:15
相关论文
共 36 条
[1]   Mice lacking phosphatidylinositol transfer protein-α exhibit spinocerebellar degeneration, intestinal and hepatic steatosis, and hypoglycemia [J].
Alb, JG ;
Cortese, JD ;
Phillips, SE ;
Albin, RL ;
Nagy, TR ;
Hamilton, BA ;
Bankaitis, VA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (35) :33501-33518
[2]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[3]   Mass spectrometric analysis reveals an increase in plasma membrane polyunsaturated phospholipid species upon cellular cholesterol loading [J].
Blom, TS ;
Koivusalo, M ;
Kuismanen, E ;
Kostiainen, R ;
Somerharju, P ;
Ikonen, E .
BIOCHEMISTRY, 2001, 40 (48) :14635-14644
[4]   Quantitative analysis of biological membrane lipids at the low picomole level by nano-electrospray ionization tandem mass spectrometry [J].
Brugger, B ;
Erben, G ;
Sandhoff, R ;
Wieland, FT ;
Lehmann, WD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) :2339-2344
[5]   Hyperlipidaemia and cardiovascular disease [J].
Cozma, LS .
CURRENT OPINION IN LIPIDOLOGY, 2002, 13 (02) :227-229
[6]  
DeLong CJ, 2001, J LIPID RES, V42, P1959
[7]   Quantitative profiling of phospholipids by multiple precursor ion scanning on a hybrid quadrupole time-of-flight mass spectrometer [J].
Ekroos, K ;
Chernushevich, IV ;
Simons, K ;
Shevchenko, A .
ANALYTICAL CHEMISTRY, 2002, 74 (05) :941-949
[8]   Liver peroxisome proliferator-activated receptor γ contributes to hepatic steatosis, triglyceride clearance, and regulation of body fat mass [J].
Gavrilova, O ;
Haluzik, M ;
Matsusue, K ;
Cutson, JJ ;
Johnson, L ;
Dietz, KR ;
Nicol, CJ ;
Vinson, C ;
Gonzalez, FJ ;
Reitman, ML .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (36) :34268-34276
[9]   Tandem mass spectrometry in the study of fatty acids, bile acids, and steroids [J].
Griffiths, WJ .
MASS SPECTROMETRY REVIEWS, 2003, 22 (02) :81-152
[10]  
HAN X, 2004, IN PRESS MASS SPECTR