Quantitative measurement of different ceramide species from crude cellular extracts by normal-phase high-performance liquid chromatography coupled to atmospheric pressure ionization mass spectrometry
Normal‐phase high‐performance liquid chromatography (NP‐HPLC) coupled to atmospheric pressure ionization mass spectrometry (APCI‐MS) allows quantitative analysis of endogenous ceramide and dihydroceramide species from crude lipid extracts. Qualitative information for the species comes from observati...
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description | Normal‐phase high‐performance liquid chromatography (NP‐HPLC) coupled to atmospheric pressure ionization mass spectrometry (APCI‐MS) allows quantitative analysis of endogenous ceramide and dihydroceramide species from crude lipid extracts. Qualitative information for the species comes from observation of differences in chromatographic and mass spectrometric behavior between species (Pettus et al. Rapid Commun. Mass Spectrom. 2003; 17: 1017–1026). Quantitative analysis is achieved by (1) use of a synthetic internal standard as an extraction and injection control, (2) lack of salt adduction, ion suppression, or other matrix effects in APCI mode, and (3) consistent fragmentation and ionization of external standards across the physiologically relevant concentration range found in endogenous lipid samples. Application to the analysis and quantitation of ceramide and dihydroceramide from various cell lines is demonstrated. The results from APCI‐MS analysis corroborate and enhance information acquired from use of the diacylglycerol kinase assay for total ceramide measurement. This technique readily allows simultaneous quantitation of ceramide and dihydroceramide species. Copyright © 2004 John Wiley & Sons, Ltd. |
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Qualitative information for the species comes from observation of differences in chromatographic and mass spectrometric behavior between species (Pettus et al. Rapid Commun. Mass Spectrom. 2003; 17: 1017–1026). Quantitative analysis is achieved by (1) use of a synthetic internal standard as an extraction and injection control, (2) lack of salt adduction, ion suppression, or other matrix effects in APCI mode, and (3) consistent fragmentation and ionization of external standards across the physiologically relevant concentration range found in endogenous lipid samples. Application to the analysis and quantitation of ceramide and dihydroceramide from various cell lines is demonstrated. The results from APCI‐MS analysis corroborate and enhance information acquired from use of the diacylglycerol kinase assay for total ceramide measurement. This technique readily allows simultaneous quantitation of ceramide and dihydroceramide species. Copyright © 2004 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0951-4198</identifier><identifier>EISSN: 1097-0231</identifier><identifier>DOI: 10.1002/rcm.1373</identifier><identifier>PMID: 14978803</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Animals ; Cell Extracts - chemistry ; Ceramides - analysis ; Chromatography, High Pressure Liquid - methods ; Female ; HL-60 Cells - chemistry ; Humans ; Spectrometry, Mass, Electrospray Ionization - methods</subject><ispartof>Rapid communications in mass spectrometry, 2004-01, Vol.18 (5), p.577-583</ispartof><rights>Copyright © 2004 John Wiley & Sons, Ltd.</rights><rights>Copyright 2004 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4213-c2eae951b87c5135f3ee9e046302f33fb6bb63690bffcec52fef801fc467047e3</citedby><cites>FETCH-LOGICAL-c4213-c2eae951b87c5135f3ee9e046302f33fb6bb63690bffcec52fef801fc467047e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Frcm.1373$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Frcm.1373$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14978803$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pettus, Benjamin J.</creatorcontrib><creatorcontrib>Kroesen, Bart-Jan</creatorcontrib><creatorcontrib>Szulc, Zdizslaw M.</creatorcontrib><creatorcontrib>Bielawska, Alicia</creatorcontrib><creatorcontrib>Bielawski, Jacek</creatorcontrib><creatorcontrib>Hannun, Yusuf A.</creatorcontrib><creatorcontrib>Busman, Mark</creatorcontrib><title>Quantitative measurement of different ceramide species from crude cellular extracts by normal-phase high-performance liquid chromatography coupled to atmospheric pressure ionization mass spectrometry</title><title>Rapid communications in mass spectrometry</title><addtitle>Rapid Commun. Mass Spectrom</addtitle><description>Normal‐phase high‐performance liquid chromatography (NP‐HPLC) coupled to atmospheric pressure ionization mass spectrometry (APCI‐MS) allows quantitative analysis of endogenous ceramide and dihydroceramide species from crude lipid extracts. Qualitative information for the species comes from observation of differences in chromatographic and mass spectrometric behavior between species (Pettus et al. Rapid Commun. Mass Spectrom. 2003; 17: 1017–1026). Quantitative analysis is achieved by (1) use of a synthetic internal standard as an extraction and injection control, (2) lack of salt adduction, ion suppression, or other matrix effects in APCI mode, and (3) consistent fragmentation and ionization of external standards across the physiologically relevant concentration range found in endogenous lipid samples. Application to the analysis and quantitation of ceramide and dihydroceramide from various cell lines is demonstrated. The results from APCI‐MS analysis corroborate and enhance information acquired from use of the diacylglycerol kinase assay for total ceramide measurement. This technique readily allows simultaneous quantitation of ceramide and dihydroceramide species. Copyright © 2004 John Wiley & Sons, Ltd.</description><subject>Animals</subject><subject>Cell Extracts - chemistry</subject><subject>Ceramides - analysis</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Female</subject><subject>HL-60 Cells - chemistry</subject><subject>Humans</subject><subject>Spectrometry, Mass, Electrospray Ionization - methods</subject><issn>0951-4198</issn><issn>1097-0231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1u1TAQRi0EopeCxBMgrxCbFDvO7xJdaEG6gEAXsbQcZ9wY4jgdO7ThBXktEm4EK1ajGR0dfZqPkKecXXDG0peo3QUXpbhHdpzVZcJSwe-THatznmS8rs7IoxC-McZ5nrKH5IxndVlVTOzIr0-TGqKNKtofQB2oMCE4GCL1hrbWGMB10YDK2RZoGEFbCNSgd1TjtJw09P3UK6RwF1HpGGgz08GjU30ydioA7ex1l4yAZj0OGmhvbybbUt0tFhX9Naqxm6n209hDS6OnKjofxg7QajoihDUVtX6wP5egfqBOhfAnS1wMEHF-TB4Y1Qd4ss1z8uXyzXH_Njl8vHq3f3VIdJZykegUFCxfaapS51zkRgDUwLJCsNQIYZqiaQpR1KwxRoPOUwOmYtzorChZVoI4J89P3hH9zQQhSmfD-gE1gJ-CXOAyZyxbwBcnUKMPAcHIEa1TOEvO5FqaXEqTa2kL-mxzTo2D9h-4tbQAyQm4tT3M_xXJz_v3m3DjbYhw95dX-F0WpShz-fXDlTxUR3E8VIV8LX4DWAK3qQ</recordid><startdate>20040101</startdate><enddate>20040101</enddate><creator>Pettus, Benjamin J.</creator><creator>Kroesen, Bart-Jan</creator><creator>Szulc, Zdizslaw M.</creator><creator>Bielawska, Alicia</creator><creator>Bielawski, Jacek</creator><creator>Hannun, Yusuf A.</creator><creator>Busman, Mark</creator><general>John Wiley & Sons, Ltd</general><scope>BSCLL</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>7X8</scope></search><sort><creationdate>20040101</creationdate><title>Quantitative measurement of different ceramide species from crude cellular extracts by normal-phase high-performance liquid chromatography coupled to atmospheric pressure ionization mass spectrometry</title><author>Pettus, Benjamin J. ; Kroesen, Bart-Jan ; Szulc, Zdizslaw M. ; Bielawska, Alicia ; Bielawski, Jacek ; Hannun, Yusuf A. ; Busman, Mark</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4213-c2eae951b87c5135f3ee9e046302f33fb6bb63690bffcec52fef801fc467047e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Cell Extracts - chemistry</topic><topic>Ceramides - analysis</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Female</topic><topic>HL-60 Cells - chemistry</topic><topic>Humans</topic><topic>Spectrometry, Mass, Electrospray Ionization - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pettus, Benjamin J.</creatorcontrib><creatorcontrib>Kroesen, Bart-Jan</creatorcontrib><creatorcontrib>Szulc, Zdizslaw M.</creatorcontrib><creatorcontrib>Bielawska, Alicia</creatorcontrib><creatorcontrib>Bielawski, Jacek</creatorcontrib><creatorcontrib>Hannun, Yusuf A.</creatorcontrib><creatorcontrib>Busman, Mark</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Rapid communications in mass spectrometry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pettus, Benjamin J.</au><au>Kroesen, Bart-Jan</au><au>Szulc, Zdizslaw M.</au><au>Bielawska, Alicia</au><au>Bielawski, Jacek</au><au>Hannun, Yusuf A.</au><au>Busman, Mark</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantitative measurement of different ceramide species from crude cellular extracts by normal-phase high-performance liquid chromatography coupled to atmospheric pressure ionization mass spectrometry</atitle><jtitle>Rapid communications in mass spectrometry</jtitle><addtitle>Rapid Commun. Mass Spectrom</addtitle><date>2004-01-01</date><risdate>2004</risdate><volume>18</volume><issue>5</issue><spage>577</spage><epage>583</epage><pages>577-583</pages><issn>0951-4198</issn><eissn>1097-0231</eissn><abstract>Normal‐phase high‐performance liquid chromatography (NP‐HPLC) coupled to atmospheric pressure ionization mass spectrometry (APCI‐MS) allows quantitative analysis of endogenous ceramide and dihydroceramide species from crude lipid extracts. Qualitative information for the species comes from observation of differences in chromatographic and mass spectrometric behavior between species (Pettus et al. Rapid Commun. Mass Spectrom. 2003; 17: 1017–1026). Quantitative analysis is achieved by (1) use of a synthetic internal standard as an extraction and injection control, (2) lack of salt adduction, ion suppression, or other matrix effects in APCI mode, and (3) consistent fragmentation and ionization of external standards across the physiologically relevant concentration range found in endogenous lipid samples. Application to the analysis and quantitation of ceramide and dihydroceramide from various cell lines is demonstrated. The results from APCI‐MS analysis corroborate and enhance information acquired from use of the diacylglycerol kinase assay for total ceramide measurement. This technique readily allows simultaneous quantitation of ceramide and dihydroceramide species. Copyright © 2004 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>14978803</pmid><doi>10.1002/rcm.1373</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Cell Extracts - chemistry Ceramides - analysis Chromatography, High Pressure Liquid - methods Female HL-60 Cells - chemistry Humans Spectrometry, Mass, Electrospray Ionization - methods |
title | Quantitative measurement of different ceramide species from crude cellular extracts by normal-phase high-performance liquid chromatography coupled to atmospheric pressure ionization mass spectrometry |
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