A complete workflow for high-resolution spectral-stitching nanoelectrospray direct-infusion mass-spectrometry-based metabolomics and lipidomics

被引:123
作者
Southam, Andrew D. [1 ]
Weber, Ralf J. M. [1 ]
Engel, Jasper [2 ]
Jones, Martin R. [1 ]
Viant, Mark R. [1 ,2 ]
机构
[1] Univ Birmingham, Sch Biosci, Birmingham, W Midlands, England
[2] Univ Birmingham, NERC Biomol Anal Facil Metabol Node NBAF B, Birmingham, W Midlands, England
基金
英国生物技术与生命科学研究理事会; 英国自然环境研究理事会;
关键词
HIGH-THROUGHPUT; FT-ICR; METABOLITE EXTRACTION; SHOTGUN LIPIDOMICS; DAPHNIA-MAGNA; SAMPLES; CELLS; NMR; MS; QUANTIFICATION;
D O I
10.1038/nprot.2016.156
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Metabolomic and lipidomic studies measure and discover metabolic and lipid profiles in biological samples, enabling a better understanding of the metabolism of specific biological phenotypes. Accurate biological interpretations require high analytical reproducibility and sensitivity, and standardized and transparent data processing. Here we describe a complete workflow for nanoelectrospray ionization (nESI) direct-infusion mass spectrometry (DIMS) metabolomics and lipidomics. After metabolite and lipid extraction from tissues and biofluids, samples are directly infused into a high-resolution mass spectrometer (e.g., Orbitrap) using a chip-based nESESI sample delivery system. nESESI functions to minimize ionization suppression or enhancement effects as compared with standard electrospray ionization (ESI). Our analytical technique-named spectral stitching-measures data as several overlapping mass-to-charge (m/z) windows that are subsequently 'stitched' together, creating a complete mass spectrum. This considerably increases the dynamic range and detection sensitivity-about a fivefold increase in peak detection-as compared with the collection of DIMS data as a single wide mass-to-charge (m/z ratio) window. Data processing, statistical analysis and metabolite annotation are executed as a workflow within the user-friendly, transparent and freely available Galaxy platform (galaxyproject.org). Generated data have high mass accuracy that enables molecular formulae peak annotations. The workflow is compatible with any sample-extraction method; in this protocol, the examples are extracted using a biphasic method, with methanol, chloroform and water as the solvents. The complete workflow is reproducible, rapid and automated, which enables cost-effective analysis of > 10,000 samples per year, making it ideal for high-throughput metabolomics and lipidomics screening-e.g., for clinical phenotyping, drug screening and toxicity testing.
引用
收藏
页码:310 / 328
页数:19
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