Simultaneous extraction of metabolome and lipidome with methyl tert-butyl ether from a single small tissue sample for ultra-high performance liquid chromatography/mass spectrometry
•A strategy for the simultaneous extraction of lipidome and metabolome from a small tissue sample.•Even a small mouse muscle of 2.5mg dry weight is sufficient.•Equal volumes from the polar and lipophilic phases of an MTBE extraction are mixed for metabolomics.•An aliquot of the lipophilic phase of a...
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creator | Chen, Shili Hoene, Miriam Li, Jia Li, Yanjie Zhao, Xinjie Häring, Hans-Ulrich Schleicher, Erwin D. Weigert, Cora Xu, Guowang Lehmann, Rainer |
description | •A strategy for the simultaneous extraction of lipidome and metabolome from a small tissue sample.•Even a small mouse muscle of 2.5mg dry weight is sufficient.•Equal volumes from the polar and lipophilic phases of an MTBE extraction are mixed for metabolomics.•An aliquot of the lipophilic phase of an MTBE extraction is used for lipidomics.•Valuable tissue can be saved for complementary analyses when only a limited amount of sample is available.
A common challenge for scientists working with animal tissue or human biopsy samples is the limitation of material and consequently, the difficulty to perform comprehensive metabolic profiling within one experiment. Here, we present a novel approach to simultaneously perform targeted and non-targeted metabolomics as well as lipidomics from one small piece of liver or muscle tissue by ultra-high performance liquid chromatography/mass spectrometry (UHPLC/MS) following a methyl tert-butyl ether (MTBE)-based extraction. Equal relative amounts of the resulting polar and non-polar fractions were pooled, evaporated and reconstituted in the appropriate solvent for UHPLC/MS analysis. This mix was comparable or superior in yield and reproducibility to a standard 80% methanol extraction for the profiling of polar and lipophilic metabolites (free carnitine, acylcarnitines and FFA). The mix was also suitable for non-targeted metabolomics, an easy measure to increase the metabolite coverage by 30% relative to using the polar fraction alone. Lipidomics was performed from an aliquot of the non-polar fraction. This novel strategy could successfully be applied to one mouse soleus muscle with a dry weight of merely 2.5mg. By enabling a simultaneous profiling of lipids and metabolites with mixed polarity while saving material for molecular, biochemical or histological analyses, our approach may open up new perspectives toward a comprehensive investigation of small, valuable tissue samples. |
doi_str_mv | 10.1016/j.chroma.2013.05.019 |
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A common challenge for scientists working with animal tissue or human biopsy samples is the limitation of material and consequently, the difficulty to perform comprehensive metabolic profiling within one experiment. Here, we present a novel approach to simultaneously perform targeted and non-targeted metabolomics as well as lipidomics from one small piece of liver or muscle tissue by ultra-high performance liquid chromatography/mass spectrometry (UHPLC/MS) following a methyl tert-butyl ether (MTBE)-based extraction. Equal relative amounts of the resulting polar and non-polar fractions were pooled, evaporated and reconstituted in the appropriate solvent for UHPLC/MS analysis. This mix was comparable or superior in yield and reproducibility to a standard 80% methanol extraction for the profiling of polar and lipophilic metabolites (free carnitine, acylcarnitines and FFA). The mix was also suitable for non-targeted metabolomics, an easy measure to increase the metabolite coverage by 30% relative to using the polar fraction alone. Lipidomics was performed from an aliquot of the non-polar fraction. This novel strategy could successfully be applied to one mouse soleus muscle with a dry weight of merely 2.5mg. By enabling a simultaneous profiling of lipids and metabolites with mixed polarity while saving material for molecular, biochemical or histological analyses, our approach may open up new perspectives toward a comprehensive investigation of small, valuable tissue samples.</description><identifier>ISSN: 0021-9673</identifier><identifier>EISSN: 1873-3778</identifier><identifier>DOI: 10.1016/j.chroma.2013.05.019</identifier><identifier>PMID: 23743007</identifier><identifier>CODEN: JOCRAM</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Analytical chemistry ; Analytical, structural and metabolic biochemistry ; Animals ; Biological and medical sciences ; Biopsy ; Chemistry ; Chromatographic methods and physical methods associated with chromatography ; Chromatography, High Pressure Liquid - methods ; Exact sciences and technology ; Fundamental and applied biological sciences. Psychology ; Lipids ; Liquid chromatography/mass spectrometry ; Liver - metabolism ; Male ; Mass Spectrometry ; Metabolic profiling ; Metabolomics ; Metabolomics - methods ; Methyl Ethers - metabolism ; Methyl tert-butyl ether (MTBE) ; Mice ; Mice, Inbred C57BL ; Muscles - metabolism ; Other biological molecules ; Other chromatographic methods ; Sample pretreatment</subject><ispartof>Journal of Chromatography A, 2013-07, Vol.1298, p.9-16</ispartof><rights>2013 Elsevier B.V.</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2013 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c425t-fd282294f05546f1712541b738568a0cb5767d6fc6ffbff170373ac65b278eac3</citedby><cites>FETCH-LOGICAL-c425t-fd282294f05546f1712541b738568a0cb5767d6fc6ffbff170373ac65b278eac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0021967313007693$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27499241$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23743007$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Shili</creatorcontrib><creatorcontrib>Hoene, Miriam</creatorcontrib><creatorcontrib>Li, Jia</creatorcontrib><creatorcontrib>Li, Yanjie</creatorcontrib><creatorcontrib>Zhao, Xinjie</creatorcontrib><creatorcontrib>Häring, Hans-Ulrich</creatorcontrib><creatorcontrib>Schleicher, Erwin D.</creatorcontrib><creatorcontrib>Weigert, Cora</creatorcontrib><creatorcontrib>Xu, Guowang</creatorcontrib><creatorcontrib>Lehmann, Rainer</creatorcontrib><title>Simultaneous extraction of metabolome and lipidome with methyl tert-butyl ether from a single small tissue sample for ultra-high performance liquid chromatography/mass spectrometry</title><title>Journal of Chromatography A</title><addtitle>J Chromatogr A</addtitle><description>•A strategy for the simultaneous extraction of lipidome and metabolome from a small tissue sample.•Even a small mouse muscle of 2.5mg dry weight is sufficient.•Equal volumes from the polar and lipophilic phases of an MTBE extraction are mixed for metabolomics.•An aliquot of the lipophilic phase of an MTBE extraction is used for lipidomics.•Valuable tissue can be saved for complementary analyses when only a limited amount of sample is available.
A common challenge for scientists working with animal tissue or human biopsy samples is the limitation of material and consequently, the difficulty to perform comprehensive metabolic profiling within one experiment. Here, we present a novel approach to simultaneously perform targeted and non-targeted metabolomics as well as lipidomics from one small piece of liver or muscle tissue by ultra-high performance liquid chromatography/mass spectrometry (UHPLC/MS) following a methyl tert-butyl ether (MTBE)-based extraction. Equal relative amounts of the resulting polar and non-polar fractions were pooled, evaporated and reconstituted in the appropriate solvent for UHPLC/MS analysis. This mix was comparable or superior in yield and reproducibility to a standard 80% methanol extraction for the profiling of polar and lipophilic metabolites (free carnitine, acylcarnitines and FFA). The mix was also suitable for non-targeted metabolomics, an easy measure to increase the metabolite coverage by 30% relative to using the polar fraction alone. Lipidomics was performed from an aliquot of the non-polar fraction. This novel strategy could successfully be applied to one mouse soleus muscle with a dry weight of merely 2.5mg. By enabling a simultaneous profiling of lipids and metabolites with mixed polarity while saving material for molecular, biochemical or histological analyses, our approach may open up new perspectives toward a comprehensive investigation of small, valuable tissue samples.</description><subject>Analytical chemistry</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>Chemistry</subject><subject>Chromatographic methods and physical methods associated with chromatography</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Exact sciences and technology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Lipids</subject><subject>Liquid chromatography/mass spectrometry</subject><subject>Liver - metabolism</subject><subject>Male</subject><subject>Mass Spectrometry</subject><subject>Metabolic profiling</subject><subject>Metabolomics</subject><subject>Metabolomics - methods</subject><subject>Methyl Ethers - metabolism</subject><subject>Methyl tert-butyl ether (MTBE)</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Muscles - metabolism</subject><subject>Other biological molecules</subject><subject>Other chromatographic methods</subject><subject>Sample pretreatment</subject><issn>0021-9673</issn><issn>1873-3778</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UcuO1DAQjBCIHRb-ACFfkLhk1o84Ti5IaMVLWokDcLYcx554ZMdZ21mY_-ID6VEGuHFqd3W1u7uqql4SvCeYtDfHvZ5SDGpPMWF7zPeY9I-qHekEq5kQ3eNqhzEldd8KdlU9y_mIMRFY0KfVFWWiYRiLXfXrqwurL2o2cc3I_CxJ6eLijKJFwRQ1RB-DQWoekXeLG8_JD1emc3E6eVRMKvWwFngCYBKysBNSKLv54A3KQXkguZxXSFRYALMxIRiZVD25w4QWkwAJatYGRtyvbkTbYSUeklqm001QOaO8GF0ANiWdnldPrPLZvLjE6-r7h_ffbj_Vd18-fr59d1frhvJS25F2lPaNxZw3rSWCUN6QQbCOt53CeuCiFWNrdWvtYKGOmWBKt3ygojNKs-vqzfbvkuL9anKRwWVtvN_kkqRlHJMOAlCbjapTzDkZK5fkgkonSbA8-yWPcjtLnv2SmEvwC9peXSasQzDj36Y_BgHh9YWgslbeJtDJ5X880fQ9bQjw3m48A3o8OJNk1s6ApqNLIJwco_v_Jr8BFDO6-A</recordid><startdate>20130712</startdate><enddate>20130712</enddate><creator>Chen, Shili</creator><creator>Hoene, Miriam</creator><creator>Li, Jia</creator><creator>Li, Yanjie</creator><creator>Zhao, Xinjie</creator><creator>Häring, Hans-Ulrich</creator><creator>Schleicher, Erwin D.</creator><creator>Weigert, Cora</creator><creator>Xu, Guowang</creator><creator>Lehmann, Rainer</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><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>7QH</scope><scope>7UA</scope><scope>C1K</scope><scope>F1W</scope><scope>H97</scope><scope>L.G</scope></search><sort><creationdate>20130712</creationdate><title>Simultaneous extraction of metabolome and lipidome with methyl tert-butyl ether from a single small tissue sample for ultra-high performance liquid chromatography/mass spectrometry</title><author>Chen, Shili ; Hoene, Miriam ; Li, Jia ; Li, Yanjie ; Zhao, Xinjie ; Häring, Hans-Ulrich ; Schleicher, Erwin D. ; Weigert, Cora ; Xu, Guowang ; Lehmann, Rainer</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c425t-fd282294f05546f1712541b738568a0cb5767d6fc6ffbff170373ac65b278eac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Analytical chemistry</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biopsy</topic><topic>Chemistry</topic><topic>Chromatographic methods and physical methods associated with chromatography</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Exact sciences and technology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Lipids</topic><topic>Liquid chromatography/mass spectrometry</topic><topic>Liver - metabolism</topic><topic>Male</topic><topic>Mass Spectrometry</topic><topic>Metabolic profiling</topic><topic>Metabolomics</topic><topic>Metabolomics - methods</topic><topic>Methyl Ethers - metabolism</topic><topic>Methyl tert-butyl ether (MTBE)</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Muscles - metabolism</topic><topic>Other biological molecules</topic><topic>Other chromatographic methods</topic><topic>Sample pretreatment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Shili</creatorcontrib><creatorcontrib>Hoene, Miriam</creatorcontrib><creatorcontrib>Li, Jia</creatorcontrib><creatorcontrib>Li, Yanjie</creatorcontrib><creatorcontrib>Zhao, Xinjie</creatorcontrib><creatorcontrib>Häring, Hans-Ulrich</creatorcontrib><creatorcontrib>Schleicher, Erwin D.</creatorcontrib><creatorcontrib>Weigert, Cora</creatorcontrib><creatorcontrib>Xu, Guowang</creatorcontrib><creatorcontrib>Lehmann, Rainer</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aqualine</collection><collection>Water Resources Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><jtitle>Journal of Chromatography A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Shili</au><au>Hoene, Miriam</au><au>Li, Jia</au><au>Li, Yanjie</au><au>Zhao, Xinjie</au><au>Häring, Hans-Ulrich</au><au>Schleicher, Erwin D.</au><au>Weigert, Cora</au><au>Xu, Guowang</au><au>Lehmann, Rainer</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Simultaneous extraction of metabolome and lipidome with methyl tert-butyl ether from a single small tissue sample for ultra-high performance liquid chromatography/mass spectrometry</atitle><jtitle>Journal of Chromatography A</jtitle><addtitle>J Chromatogr A</addtitle><date>2013-07-12</date><risdate>2013</risdate><volume>1298</volume><spage>9</spage><epage>16</epage><pages>9-16</pages><issn>0021-9673</issn><eissn>1873-3778</eissn><coden>JOCRAM</coden><abstract>•A strategy for the simultaneous extraction of lipidome and metabolome from a small tissue sample.•Even a small mouse muscle of 2.5mg dry weight is sufficient.•Equal volumes from the polar and lipophilic phases of an MTBE extraction are mixed for metabolomics.•An aliquot of the lipophilic phase of an MTBE extraction is used for lipidomics.•Valuable tissue can be saved for complementary analyses when only a limited amount of sample is available.
A common challenge for scientists working with animal tissue or human biopsy samples is the limitation of material and consequently, the difficulty to perform comprehensive metabolic profiling within one experiment. Here, we present a novel approach to simultaneously perform targeted and non-targeted metabolomics as well as lipidomics from one small piece of liver or muscle tissue by ultra-high performance liquid chromatography/mass spectrometry (UHPLC/MS) following a methyl tert-butyl ether (MTBE)-based extraction. Equal relative amounts of the resulting polar and non-polar fractions were pooled, evaporated and reconstituted in the appropriate solvent for UHPLC/MS analysis. This mix was comparable or superior in yield and reproducibility to a standard 80% methanol extraction for the profiling of polar and lipophilic metabolites (free carnitine, acylcarnitines and FFA). The mix was also suitable for non-targeted metabolomics, an easy measure to increase the metabolite coverage by 30% relative to using the polar fraction alone. Lipidomics was performed from an aliquot of the non-polar fraction. This novel strategy could successfully be applied to one mouse soleus muscle with a dry weight of merely 2.5mg. By enabling a simultaneous profiling of lipids and metabolites with mixed polarity while saving material for molecular, biochemical or histological analyses, our approach may open up new perspectives toward a comprehensive investigation of small, valuable tissue samples.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>23743007</pmid><doi>10.1016/j.chroma.2013.05.019</doi><tpages>8</tpages></addata></record> |
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subjects | Analytical chemistry Analytical, structural and metabolic biochemistry Animals Biological and medical sciences Biopsy Chemistry Chromatographic methods and physical methods associated with chromatography Chromatography, High Pressure Liquid - methods Exact sciences and technology Fundamental and applied biological sciences. Psychology Lipids Liquid chromatography/mass spectrometry Liver - metabolism Male Mass Spectrometry Metabolic profiling Metabolomics Metabolomics - methods Methyl Ethers - metabolism Methyl tert-butyl ether (MTBE) Mice Mice, Inbred C57BL Muscles - metabolism Other biological molecules Other chromatographic methods Sample pretreatment |
title | Simultaneous extraction of metabolome and lipidome with methyl tert-butyl ether from a single small tissue sample for ultra-high performance liquid chromatography/mass spectrometry |
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