Sample normalization methods in quantitative metabolomics

被引:205
作者
Wu, Yiman [1 ]
Li, Liang [1 ]
机构
[1] Univ Alberta, Dept Chem, Edmonton, AB T6G 2G2, Canada
关键词
Metabolomics; Quantitative metabolomic profiling; Metabolite quantification; Sample normalization; Liquid chromatography; Mass spectrometry; EXHALED BREATH CONDENSATE; LIQUID CHROMATOGRAPHY/MASS SPECTROMETRY; TANDEM MASS-SPECTROMETRY; ION SUPPRESSION METHOD; LABELING LC-MS; URINARY CREATININE; RELATIVE QUANTIFICATION; GAS-CHROMATOGRAPHY; LARGE-SCALE; EXPERIMENTAL-DESIGN;
D O I
10.1016/j.chroma.2015.12.007
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
To reveal metabolomic changes caused by a biological event in quantitative metabolomics, it is critical to use an analytical tool that can perform accurate and precise quantification to examine the true concentration differences of individual metabolites found in different samples. A number of steps are involved in metabolomic analysis including pre-analytical work (e.g., sample collection and storage), analytical work (e.g., sample analysis) and data analysis (e.g., feature extraction and quantification). Each one of them can influence the quantitative results significantly and thus should be performed with great care. Among them, the total sample amount or concentration of metabolites can be significantly different from one sample to another. Thus, it is critical to reduce or eliminate the effect of total sample amount variation on quantification of individual metabolites. In this review, we describe the importance of sample normalization in the analytical workflow with a focus on mass spectrometry (MS)-based platforms, discuss a number of methods recently reported in the literature and comment on their applicability in real world metabolomics applications. Sample normalization has been sometimes ignored in metabolomics, partially due to the lack of a convenient means of performing sample normalization. We show that several methods are now available and sample normalization should be performed in quantitative metabolomics where the analyzed samples have significant variations in total sample amounts. (c) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:80 / 95
页数:16
相关论文
共 101 条
[1]
Development of a new method for improved identification and relative quantification of unknown metabolites in complex samples: Determination of a triterpenoid metabolic fingerprint for the in situ characterization of Ganoderma bioactive compounds [J].
Adamec, Jiri ;
Jannasch, Amber ;
Dudhgaonkar, Shailesh ;
Jedinak, Andrej ;
Sedlak, Miroslav ;
Sliva, Daniel .
JOURNAL OF SEPARATION SCIENCE, 2009, 32 (23-24) :4052-4058
[2]
RELIABILITY OF URINARY CREATININE AS A PARAMETER USED TO ADJUST VALUES OF URINARY BIOLOGICAL INDICATORS [J].
ALESSIO, L ;
BERLIN, A ;
DELLORTO, A ;
TOFFOLETTO, F ;
GHEZZI, I .
INTERNATIONAL ARCHIVES OF OCCUPATIONAL AND ENVIRONMENTAL HEALTH, 1985, 55 (02) :99-106
[3]
Metabolomics analysis I. Selection of biological samples and practical aspects preceding sample preparation [J].
Alvarez-Sanchez, B. ;
Priego-Capote, F. ;
Luque de Castro, M. D. .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2010, 29 (02) :111-119
[4]
Pre-Analytical Sample Quality: Metabolite Ratios as an Intrinsic Marker for Prolonged Room Temperature Exposure of Serum Samples [J].
Anton, Gabriele ;
Wilson, Rory ;
Yu, Zhong-hao ;
Prehn, Cornelia ;
Zukunft, Sven ;
Adamski, Jerzy ;
Heier, Margit ;
Meisinger, Christa ;
Roemisch-Margl, Werner ;
Wang-Sattler, Rui ;
Hveem, Kristian ;
Wolffenbuttel, Bruce ;
Peters, Annette ;
Kastenmueller, Gabi ;
Waldenberger, Melanie .
PLOS ONE, 2015, 10 (03)
[5]
Determination of the volume of sweat accumulated in a sweat-patch using sodium and potassium as internal reference [J].
Appenzeller, Brice M. R. ;
Schummer, Claude ;
Rodrigues, Sophie Boura ;
Wennig, Robert .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2007, 852 (1-2) :333-337
[6]
The Human Urine Metabolome [J].
Bouatra, Souhaila ;
Aziat, Farid ;
Mandal, Rupasri ;
Guo, An Chi ;
Wilson, Michael R. ;
Knox, Craig ;
Bjorndahl, Trent C. ;
Krishnamurthy, Ramanarayan ;
Saleem, Fozia ;
Liu, Philip ;
Dame, Zerihun T. ;
Poelzer, Jenna ;
Huynh, Jessica ;
Yallou, Faizath S. ;
Psychogios, Nick ;
Dong, Edison ;
Bogumil, Ralf ;
Roehring, Cornelia ;
Wishart, David S. .
PLOS ONE, 2013, 8 (09)
[7]
Isotopic labeling-assisted metabolomics using LC-MS [J].
Bueschl, C. ;
Krska, R. ;
Kluger, B. ;
Schuhmacher, R. .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2013, 405 (01) :27-33
[8]
Normalization of urinary pteridines by urine specific gravity for early cancer detection [J].
Burton, Casey ;
Shi, Honglan ;
Ma, Yinfa .
CLINICA CHIMICA ACTA, 2014, 435 :42-47
[9]
Simultaneous Detection of Six Urinary Pteridines and Creatinine by High-Performance Liquid Chromatography-Tandem Mass Spectrometry for Clinical Breast Cancer Detection [J].
Burton, Casey ;
Shi, Honglan ;
Ma, Yinfa .
ANALYTICAL CHEMISTRY, 2013, 85 (22) :11137-11145
[10]
GC-TOFMS analysis of metabolites in adherent MDCK cells and a novel strategy for identifying intracellular metabolic markers for use as cell amount indicators in data normalization [J].
Cao, Bei ;
Aa, Jiye ;
Wang, Guangji ;
Wu, Xiaolan ;
Liu, Linsheng ;
Li, Mengjie ;
Shi, Jian ;
Wang, Xinwen ;
Zhao, Chunyan ;
Zheng, Tian ;
Guo, Sheng ;
Duan, Jinao .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2011, 400 (09) :2983-2993