Metabolic profiling, metabolomic and metabonomic procedures for NMR spectroscopy of urine, plasma, serum and tissue extracts

被引:1605
作者
Beckonert, Olaf [1 ]
Keun, Hector C. [1 ]
Ebbels, Timothy M. D. [1 ]
Bundy, Jacob G. [1 ]
Holmes, Elaine [1 ]
Lindon, John C. [1 ]
Nicholson, Jeremy K. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Fac Med, Dept Biomol Med, London, England
关键词
D O I
10.1038/nprot.2007.376
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Metabolic profiling, metabolomic and metabonomic studies mainly involve the multicomponent analysis of biological fluids, tissue and cell extracts using NMR spectroscopy and/or mass spectrometry (MS). We summarize the main NMR spectroscopic applications in modern metabolic research, and provide detailed protocols for biofluid (urine, serum/plasma) and tissue sample collection and preparation, including the extraction of polar and lipophilic metabolites from tissues. H-1 NMR spectroscopic techniques such as standard 1D spectroscopy, relaxation-edited, diffusion-edited and 2D J-resolved pulse sequences are widely used at the analysis stage to monitor different groups of metabolites and are described here. They are often followed by more detailed statistical analysis or additional 2D NMR analysis for biomarker discovery. The standard acquisition time per sample is 4-5 min for a simple 1D spectrum, and both preparation and analysis can be automated to allow application to high-throughput screening for clinical diagnostic and toxicological studies, as well as molecular phenotyping and functional genomics.
引用
收藏
页码:2692 / 2703
页数:12
相关论文
共 80 条
[1]   Concentration measurement by proton NMR using the ERETIC method [J].
Akoka, S ;
Barantin, L ;
Trierweiler, M .
ANALYTICAL CHEMISTRY, 1999, 71 (13) :2554-2557
[2]   Statistical experimental design and partial least squares regression analysis of biofluid metabonomic NMR and clinical chemistry data for screening of adverse drug effects [J].
Antti, H ;
Ebbels, TMD ;
Keun, HC ;
Bollard, ME ;
Beckonert, O ;
Lindon, JC ;
Nicholson, JK ;
Holmes, E .
CHEMOMETRICS AND INTELLIGENT LABORATORY SYSTEMS, 2004, 73 (01) :139-149
[3]   Metabolomic analysis using optimized NMR and statistical methods [J].
Aranibar, Nelly ;
Ott, Karl-Heinz ;
Roongta, Vikram ;
Mueller, Luciano .
ANALYTICAL BIOCHEMISTRY, 2006, 355 (01) :62-70
[4]   2-DIMENSIONAL SPECTROSCOPY - APPLICATION TO NUCLEAR MAGNETIC-RESONANCE [J].
AUE, WP ;
BARTHOLDI, E ;
ERNST, RR .
JOURNAL OF CHEMICAL PHYSICS, 1976, 64 (05) :2229-2246
[5]   HOMONUCLEAR BROAD-BAND DECOUPLING AND 2-DIMENSIONAL J-RESOLVED NMR-SPECTROSCOPY [J].
AUE, WP ;
KARHAN, J ;
ERNST, RR .
JOURNAL OF CHEMICAL PHYSICS, 1976, 64 (10) :4226-4227
[6]  
BALES JR, 1984, CLIN CHEM, V30, P1631
[7]   Visualizing metabolic changes in breast-cancer tissue using 1H-NMR spectroscopy and self-organizing maps [J].
Beckonert, O ;
Monnerjahn, K ;
Bonk, U ;
Leibfritz, D .
NMR IN BIOMEDICINE, 2003, 16 (01) :1-11
[8]   Nuclear magnetic resonance spectroscopic and principal components analysis investigations into biochemical effects of three model hepatotoxins [J].
Beckwith-Hall, BM ;
Nicholson, JK ;
Nicholls, AW ;
Foxall, PJD ;
Lindon, JC ;
Connor, SC ;
Abdi, M ;
Connelly, J ;
Holmes, E .
CHEMICAL RESEARCH IN TOXICOLOGY, 1998, 11 (04) :260-272
[9]   EFFECT OF AGING AND DIET ON PROTON NMR-SPECTRA OF RAT URINE [J].
BELL, JD ;
SADLER, PJ ;
MORRIS, VC ;
LEVANDER, OA .
MAGNETIC RESONANCE IN MEDICINE, 1991, 17 (02) :414-422
[10]   Potential of metabolomics as a functional genomics tool [J].
Bino, RJ ;
Hall, RD ;
Fiehn, O ;
Kopka, J ;
Saito, K ;
Draper, J ;
Nikolau, BJ ;
Mendes, P ;
Roessner-Tunali, U ;
Beale, MH ;
Trethewey, RN ;
Lange, BM ;
Wurtele, ES ;
Sumner, LW .
TRENDS IN PLANT SCIENCE, 2004, 9 (09) :418-425