Promises and pitfalls of untargeted metabolomics

被引:170
作者
Gertsman, Ilya [1 ]
Barshop, Bruce A. [1 ]
机构
[1] Univ Calif San Diego, Dept Pediat, Biochem Genet & Metabol Lab, 9500 Gilman Dr, La Jolla, CA 92093 USA
关键词
MASS-SPECTROMETRY DATA; FALSE DISCOVERY RATE; METABOLITE IDENTIFICATION; QUANTITATIVE METABOLOMICS; REPORTING STANDARDS; BIOLOGICAL SAMPLES; MAMMALIAN-CELLS; EXTRACTION; CHROMATOGRAPHY; STRATEGIES;
D O I
10.1007/s10545-017-0130-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Metabolomics is one of the newer omics fields, and has enabled researchers to complement genomic and protein level analysis of disease with both semi-quantitative and quantitative metabolite levels, which are the chemical mediators that constitute a given phenotype. Over more than a decade, methodologies have advanced for both targeted (quantification of specific analytes) as well as untargeted metabolomics (biomarker discovery and global metabolite profiling). Untargeted metabolomics is especially useful when there is no a priori metabolic hypothesis. Liquid chromatography coupled to mass spectrometry (LC-MS) has been the preferred choice for untargeted metabolomics, given the versatility in metabolite coverage and sensitivity of these instruments. Resolving and profiling many hundreds to thousands of metabolites with varying chemical properties in a biological sample presents unique challenges, or pitfalls. In this review, we address the various obstacles and corrective measures available in four major aspects associated with an untargeted metabolomics experiment: (1) experimental design. (2) pre-analytical (sample collection and preparation), (3) analytical (chromatography and detection), and (4) post-analytical (data processing).
引用
收藏
页码:355 / 366
页数:12
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