Breast Milk Metabolome Characterization in a Single-Phase Extraction, Multiplatform Analytical Approach

Breast milk (BM) is a biofluid that has a fundamental role in early life nutrition and has direct impact on growth, neurodevelopment, and health. Global metabolic profiling is increasingly being utilized to characterize complex metabolic changes in biological samples. However, in order to achieve br...

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Veröffentlicht in:Analytical chemistry (Washington) 2014-08, Vol.86 (16), p.8245-8252
Hauptverfasser: Villaseñor, Alma, Garcia-Perez, Isabel, Garcia, Antonia, Posma, Joram M, Fernández-López, Mariano, Nicholas, Andreas J, Modi, Neena, Holmes, Elaine, Barbas, Coral
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container_issue 16
container_start_page 8245
container_title Analytical chemistry (Washington)
container_volume 86
creator Villaseñor, Alma
Garcia-Perez, Isabel
Garcia, Antonia
Posma, Joram M
Fernández-López, Mariano
Nicholas, Andreas J
Modi, Neena
Holmes, Elaine
Barbas, Coral
description Breast milk (BM) is a biofluid that has a fundamental role in early life nutrition and has direct impact on growth, neurodevelopment, and health. Global metabolic profiling is increasingly being utilized to characterize complex metabolic changes in biological samples. However, in order to achieve broad metabolite coverage, it is necessary to employ more than one analytical platform, typically requiring multiple sample preparation protocols. In an effort to improve analytical efficiency and retain comprehensive coverage of the metabolome, a new extraction methodology was developed that successfully retains metabolites from BM in a single-phase using an optimized methyl-tert-butyl ether solvent system. We conducted this single-phase extraction procedure on a representative pool of BM, and characterized the metabolic composition using LC-QTOF-MS and GC-Q-MS for polar and lipidic metabolites. To ensure that the extraction method was reproducible and fit-for-purpose, the analytical procedure was evaluated on both platforms using 18 metabolites selected to cover a range of chromatographic retention times and biochemical classes. Having validated the method, the metabolic signature of BM composition was mapped as a metabolic reaction network highlighting interconnected biological pathways and showing that the LC-MS and GC-MS platforms targeted largely different domains of the network. Subsequently, the same protocol was applied to ascertain compositional differences between BM at week 1 (n = 10) and 4 weeks (n = 9) post-partum. This single-phase approach is more efficient in terms of time, simplicity, cost, and sample volume than the existing two-phase methods and will be suited to high-throughput metabolic profiling studies of BM.
doi_str_mv 10.1021/ac501853d
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Global metabolic profiling is increasingly being utilized to characterize complex metabolic changes in biological samples. However, in order to achieve broad metabolite coverage, it is necessary to employ more than one analytical platform, typically requiring multiple sample preparation protocols. In an effort to improve analytical efficiency and retain comprehensive coverage of the metabolome, a new extraction methodology was developed that successfully retains metabolites from BM in a single-phase using an optimized methyl-tert-butyl ether solvent system. We conducted this single-phase extraction procedure on a representative pool of BM, and characterized the metabolic composition using LC-QTOF-MS and GC-Q-MS for polar and lipidic metabolites. To ensure that the extraction method was reproducible and fit-for-purpose, the analytical procedure was evaluated on both platforms using 18 metabolites selected to cover a range of chromatographic retention times and biochemical classes. Having validated the method, the metabolic signature of BM composition was mapped as a metabolic reaction network highlighting interconnected biological pathways and showing that the LC-MS and GC-MS platforms targeted largely different domains of the network. Subsequently, the same protocol was applied to ascertain compositional differences between BM at week 1 (n = 10) and 4 weeks (n = 9) post-partum. 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We conducted this single-phase extraction procedure on a representative pool of BM, and characterized the metabolic composition using LC-QTOF-MS and GC-Q-MS for polar and lipidic metabolites. To ensure that the extraction method was reproducible and fit-for-purpose, the analytical procedure was evaluated on both platforms using 18 metabolites selected to cover a range of chromatographic retention times and biochemical classes. Having validated the method, the metabolic signature of BM composition was mapped as a metabolic reaction network highlighting interconnected biological pathways and showing that the LC-MS and GC-MS platforms targeted largely different domains of the network. Subsequently, the same protocol was applied to ascertain compositional differences between BM at week 1 (n = 10) and 4 weeks (n = 9) post-partum. This single-phase approach is more efficient in terms of time, simplicity, cost, and sample volume than the existing two-phase methods and will be suited to high-throughput metabolic profiling studies of BM.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>25058331</pmid><doi>10.1021/ac501853d</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Biochemistry
Biological
Breast
Chemical Fractionation - methods
Chromatography, Liquid - methods
Extraction
Extraction processes
Female
Gas Chromatography-Mass Spectrometry - methods
Humans
Mass Spectrometry - methods
Mathematical analysis
Metabolites
Metabolome
Metabolomics - methods
Methyl Ethers - chemistry
Milk
Milk, Human - chemistry
Milk, Human - metabolism
Networks
Platforms
Solvents
Solvents - chemistry
title Breast Milk Metabolome Characterization in a Single-Phase Extraction, Multiplatform Analytical Approach
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