Systems-Wide High-Dimensional Data Acquisition and Informatics Using Structural Mass Spectrometry Strategies

被引:24
|
作者
Sherrod, Stacy D. [1 ]
McLean, John A. [1 ]
机构
[1] Vanderbilt Univ, Dept Chem, Ctr Innovat Technol, Vanderbilt Inst Chem Biol,Vanderbilt Inst Integra, Nashville, TN 37235 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
COLLISION CROSS-SECTIONS; ION MOBILITY; METABOLOMICS; IDENTIFICATION; LIPIDOMICS; SEPARATION; SIGNATURES; PHENOTYPE; TOOLS; CELLS;
D O I
10.1373/clinchem.2015.238261
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
BACKGROUND: Untargeted multiomics data sets are obtained for samples in systems, synthetic, and chemical biology by integrating chromatographic separations with ion mobility mass spectrometry (IM-MS) analysis. The data sets are interrogated using bioinformatics strategies to organize the data for identification prioritization. CONTENT: The use of big data approaches for data mining of massive data sets in systems-wide analyses is presented. Untargeted biological data across multiomics dimensions are obtained using a variety of chromatography strategies with structural MS. Separation timescales for different techniques and the resulting data deluge when combined with IM-MS are presented. Data mining self-organizing map strategies are used to rapidly filter the data, highlighting those features describing uniqueness to the query. Examples are provided in longitudinal analyses in synthetic biology and human liver exposure to acetaminophen, and in chemical biology for natural product discovery from bacterial biomes. CONCLUSIONS: Matching the separation timescales of different forms of chromatography with IM-MS provides sufficient multiomics selectivity to perform untargeted systems-wide analyses. New data mining strategies provide a means for rapidly interrogating these data sets for feature prioritization and discovery in a range of applications in systems, synthetic, and chemical biology. (C) 2015 American Association for Clinical Chemistry
引用
收藏
页码:77 / 83
页数:7
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