Optimized metabolite extraction from blood serum for 1H nuclear magnetic resonance spectroscopy

被引:149
作者
Tiziani, Stefano [1 ]
Einwas, Abdul-Hamid [1 ]
Lodi, Alessia [1 ]
Ludwig, Christian [1 ]
Bunce, Christopher M. [2 ]
Viant, Mark R. [2 ]
Guenther, Ulrich L. [1 ]
机构
[1] Univ Birmingham, CR UK Inst Canc Studies, Henry Bldg Biomol NMR Spectroscopy, Birmingham B15 2TT, W Midlands, England
[2] Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England
基金
英国自然环境研究理事会;
关键词
metabolomics; NMR; extraction; blood; blood serum; metabolite; lipid extraction; ultrafiltration;
D O I
10.1016/j.ab.2008.01.037
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Blood serum is commonly used for clinical diagnostics because its protein composition bears a wealth of information about the health of an organism. More recently the analysis of the small molecule composition, the metabolome, has received increased attention because the metabolite composition is influenced by many diseases, by the administration of drugs and toxins, and by the diet and life style of an individual. When nuclear magnetic resonance spectroscopy is used as an analytical tool it is often preferable to remove catalytically active proteins, in. particular for longer measurements, because metabolite concentrations are otherwise in constant flux. Here we have compared different protocols for the separation of proteins and metabolites, including precipitation methods and ultrafiltration. Whereas most extraction methods involving protein precipitation deplete some metabolites, ultrafiltration is superior in retaining metabolite concentrations and offers excellent reproducibility. We also describe a new method to recover the hydrophobic fraction for ultrafiltration with good reproducibility. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:16 / 23
页数:8
相关论文
共 13 条
[1]   The comparison of plasma deproteinization methods for the detection of low-molecular-weight metabolites by 1H nuclear magnetic resonance spectroscopy [J].
Daykin, CA ;
Foxall, PJD ;
Connor, SC ;
Lindon, JC ;
Nicholson, JK .
ANALYTICAL BIOCHEMISTRY, 2002, 304 (02) :220-230
[2]   Quantitative 1H NMR spectroscopy of blood plasma metabolites [J].
de Graaf, RA ;
Behar, KL .
ANALYTICAL CHEMISTRY, 2003, 75 (09) :2100-2104
[3]   NMRLAB -: Advanced NMR data processing in MATLAB [J].
Günther, UL ;
Ludwig, C ;
Rüterjans, H .
JOURNAL OF MAGNETIC RESONANCE, 2000, 145 (02) :201-208
[4]   WATER SUPPRESSION THAT WORKS - EXCITATION SCULPTING USING ARBITRARY WAVE-FORMS AND PULSED-FIELD GRADIENTS [J].
HWANG, TL ;
SHAKA, AJ .
JOURNAL OF MAGNETIC RESONANCE SERIES A, 1995, 112 (02) :275-279
[5]  
KRIAT M, 1993, J LIPID RES, V34, P1009
[6]   QUANTITATION OF METABOLITES IN HUMAN BLOOD-SERUM BY PROTON MAGNETIC-RESONANCE SPECTROSCOPY - A COMPARATIVE-STUDY OF THE USE OF FORMATE AND TSP AS CONCENTRATION STANDARDS [J].
KRIAT, M ;
CONFORTGOUNY, S ;
VIONDURY, J ;
SCIAKY, M ;
VIOUT, P ;
COZZONE, PJ .
NMR IN BIOMEDICINE, 1992, 5 (04) :179-184
[7]   Measurement of biomolecular diffusion coefficients in blood plasma using two-dimensional H-1-H-1 diffusion-edited total-correlation NMR spectroscopy [J].
Liu, ML ;
Nicholson, JK ;
Parkinson, JA ;
Lindon, JC .
ANALYTICAL CHEMISTRY, 1997, 69 (08) :1504-1509
[8]   750-MHZ H-1 AND H-1-C-13 NMR-SPECTROSCOPY OF HUMAN BLOOD-PLASMA [J].
NICHOLSON, JK ;
FOXALL, PJD ;
SPRAUL, M ;
FARRANT, RD ;
LINDON, JC .
ANALYTICAL CHEMISTRY, 1995, 67 (05) :793-811
[9]   Optimization of protein precipitation based upon effectiveness of protein removal and ionization effect in liquid chromatography-tandem mass spectrometry [J].
Polson, C ;
Sarkar, P ;
Incledon, B ;
Raguvaran, V ;
Grant, R .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2003, 785 (02) :263-275
[10]   ON THE MECHANISM OF THE COLD ETHANOL PRECIPITATION METHOD OF PLASMA-PROTEIN FRACTIONATION [J].
VANOSS, CJ .
JOURNAL OF PROTEIN CHEMISTRY, 1989, 8 (05) :661-668