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 |
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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. 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.</description><identifier>ISSN: 0003-2700</identifier><identifier>EISSN: 1520-6882</identifier><identifier>DOI: 10.1021/ac501853d</identifier><identifier>PMID: 25058331</identifier><identifier>CODEN: ANCHAM</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>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</subject><ispartof>Analytical chemistry (Washington), 2014-08, Vol.86 (16), p.8245-8252</ispartof><rights>Copyright American Chemical Society Aug 19, 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a411t-340ed997610b1c5d5b0de1240d11ab333033356fe56ba7fc5401dc43a38ba1db3</citedby><cites>FETCH-LOGICAL-a411t-340ed997610b1c5d5b0de1240d11ab333033356fe56ba7fc5401dc43a38ba1db3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ac501853d$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ac501853d$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25058331$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Villaseñor, Alma</creatorcontrib><creatorcontrib>Garcia-Perez, Isabel</creatorcontrib><creatorcontrib>Garcia, Antonia</creatorcontrib><creatorcontrib>Posma, Joram M</creatorcontrib><creatorcontrib>Fernández-López, Mariano</creatorcontrib><creatorcontrib>Nicholas, Andreas J</creatorcontrib><creatorcontrib>Modi, Neena</creatorcontrib><creatorcontrib>Holmes, Elaine</creatorcontrib><creatorcontrib>Barbas, Coral</creatorcontrib><title>Breast Milk Metabolome Characterization in a Single-Phase Extraction, Multiplatform Analytical Approach</title><title>Analytical chemistry (Washington)</title><addtitle>Anal. Chem</addtitle><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.</description><subject>Biochemistry</subject><subject>Biological</subject><subject>Breast</subject><subject>Chemical Fractionation - methods</subject><subject>Chromatography, Liquid - methods</subject><subject>Extraction</subject><subject>Extraction processes</subject><subject>Female</subject><subject>Gas Chromatography-Mass Spectrometry - methods</subject><subject>Humans</subject><subject>Mass Spectrometry - methods</subject><subject>Mathematical analysis</subject><subject>Metabolites</subject><subject>Metabolome</subject><subject>Metabolomics - methods</subject><subject>Methyl Ethers - chemistry</subject><subject>Milk</subject><subject>Milk, Human - chemistry</subject><subject>Milk, Human - metabolism</subject><subject>Networks</subject><subject>Platforms</subject><subject>Solvents</subject><subject>Solvents - chemistry</subject><issn>0003-2700</issn><issn>1520-6882</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpl0FFLHDEQB_AglXrVPvgFJFAKLXTbmWSzt_t4PawVPCpUn5fZbNaLze6eSRZ6fvpGTkXqQ5iH_PjP8GfsGOErgsBvpBVgqWS7x2aoBGRFWYo3bAYAMhNzgAP2LoRbAETA4i07EApUKSXO2M13byhEvrLuD1-ZSM3oxt7w5Zo86Wi8vadox4HbgRP_bYcbZ7LLNQXDT__GB5I-v_DV5KLdOIrd6Hu-GMhto9Xk-GKz8SPp9RHb78gF8_5xHrLrH6dXy5_Zxa-z8-XiIqMcMWYyB9NW1bxAaFCrVjXQGhQ5tIjUSCkhPVV0RhUNzTutcsBW55Jk2RC2jTxkn3a5ae3dZEKsexu0cY4GM06hxqISsgRRFYl--I_ejpNPpyelVAFQlUIl9XmntB9D8KarN9725Lc1Qv3Qfv3cfrInj4lT05v2WT7VncDHHSAdXmx7FfQP-SWKgQ</recordid><startdate>20140819</startdate><enddate>20140819</enddate><creator>Villaseñor, Alma</creator><creator>Garcia-Perez, Isabel</creator><creator>Garcia, Antonia</creator><creator>Posma, Joram M</creator><creator>Fernández-López, Mariano</creator><creator>Nicholas, Andreas J</creator><creator>Modi, Neena</creator><creator>Holmes, Elaine</creator><creator>Barbas, Coral</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7TM</scope><scope>7U5</scope><scope>7U7</scope><scope>7U9</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope></search><sort><creationdate>20140819</creationdate><title>Breast Milk Metabolome Characterization in a Single-Phase Extraction, Multiplatform Analytical Approach</title><author>Villaseñor, Alma ; Garcia-Perez, Isabel ; Garcia, Antonia ; Posma, Joram M ; Fernández-López, Mariano ; Nicholas, Andreas J ; Modi, Neena ; Holmes, Elaine ; Barbas, Coral</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a411t-340ed997610b1c5d5b0de1240d11ab333033356fe56ba7fc5401dc43a38ba1db3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Biochemistry</topic><topic>Biological</topic><topic>Breast</topic><topic>Chemical Fractionation - methods</topic><topic>Chromatography, Liquid - methods</topic><topic>Extraction</topic><topic>Extraction processes</topic><topic>Female</topic><topic>Gas Chromatography-Mass Spectrometry - methods</topic><topic>Humans</topic><topic>Mass Spectrometry - methods</topic><topic>Mathematical analysis</topic><topic>Metabolites</topic><topic>Metabolome</topic><topic>Metabolomics - methods</topic><topic>Methyl Ethers - chemistry</topic><topic>Milk</topic><topic>Milk, Human - chemistry</topic><topic>Milk, Human - metabolism</topic><topic>Networks</topic><topic>Platforms</topic><topic>Solvents</topic><topic>Solvents - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Villaseñor, Alma</creatorcontrib><creatorcontrib>Garcia-Perez, Isabel</creatorcontrib><creatorcontrib>Garcia, Antonia</creatorcontrib><creatorcontrib>Posma, Joram M</creatorcontrib><creatorcontrib>Fernández-López, Mariano</creatorcontrib><creatorcontrib>Nicholas, Andreas J</creatorcontrib><creatorcontrib>Modi, Neena</creatorcontrib><creatorcontrib>Holmes, Elaine</creatorcontrib><creatorcontrib>Barbas, Coral</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Analytical chemistry (Washington)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Villaseñor, Alma</au><au>Garcia-Perez, Isabel</au><au>Garcia, Antonia</au><au>Posma, Joram M</au><au>Fernández-López, Mariano</au><au>Nicholas, Andreas J</au><au>Modi, Neena</au><au>Holmes, Elaine</au><au>Barbas, Coral</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Breast Milk Metabolome Characterization in a Single-Phase Extraction, Multiplatform Analytical Approach</atitle><jtitle>Analytical chemistry (Washington)</jtitle><addtitle>Anal. Chem</addtitle><date>2014-08-19</date><risdate>2014</risdate><volume>86</volume><issue>16</issue><spage>8245</spage><epage>8252</epage><pages>8245-8252</pages><issn>0003-2700</issn><eissn>1520-6882</eissn><coden>ANCHAM</coden><abstract>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.</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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