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In Situ Structural Characterization of Glycerophospholipids and Sulfatides in Brain Tissue Using MALDI-MS/MS
Lipids are major structural components of biomembranes. Negatively charged species such as phosphatidylinositol, phosphatidylserine, sulfatides, and the zwitterionic phosphatidylethanolamines are major components of the cytoplasmic surface of the cellular membrane lipid bilayer and play a key role i...
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Published in: | Journal of the American Society for Mass Spectrometry 2007, Vol.18 (1), p.17-26 |
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description | Lipids are major structural components of biomembranes. Negatively charged species such as phosphatidylinositol, phosphatidylserine, sulfatides, and the zwitterionic phosphatidylethanolamines are major components of the cytoplasmic surface of the cellular membrane lipid bilayer and play a key role in several receptors signaling functions. Lipids are not just involved in metabolic and neurological diseases; negatively charged lipids in particular play crucial roles in physiological events such as signal transduction, receptors, and enzymatic activation, as well as storage and release of therapeutic drugs and toxic chemicals in the body. Due to the importance of their role in signaling, the field of lipidomics has rapidly expanded in recent years. In the present study, direct probing of tissue slices with negative ion mode matrix assisted laser desorption/ionization mass spectrometry was employed to profile the distribution of lipids in the brain. In total, 32 lipid species consisting of phosphatidylethanolamines, phosphatidylglycerol, phosphatidylinositols, phosphatidylserines, and sulfatides were assigned. To confirm the structure of lipid species, MALDI-MS/MS analysis was conducted. Product-ion spectra obtained in negative ion mode allow for the assignment of the head groups and the fatty acid chains for the lipid species. |
doi_str_mv | 10.1016/j.jasms.2006.08.015 |
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Negatively charged species such as phosphatidylinositol, phosphatidylserine, sulfatides, and the zwitterionic phosphatidylethanolamines are major components of the cytoplasmic surface of the cellular membrane lipid bilayer and play a key role in several receptors signaling functions. Lipids are not just involved in metabolic and neurological diseases; negatively charged lipids in particular play crucial roles in physiological events such as signal transduction, receptors, and enzymatic activation, as well as storage and release of therapeutic drugs and toxic chemicals in the body. Due to the importance of their role in signaling, the field of lipidomics has rapidly expanded in recent years. In the present study, direct probing of tissue slices with negative ion mode matrix assisted laser desorption/ionization mass spectrometry was employed to profile the distribution of lipids in the brain. In total, 32 lipid species consisting of phosphatidylethanolamines, phosphatidylglycerol, phosphatidylinositols, phosphatidylserines, and sulfatides were assigned. To confirm the structure of lipid species, MALDI-MS/MS analysis was conducted. Product-ion spectra obtained in negative ion mode allow for the assignment of the head groups and the fatty acid chains for the lipid species.</description><identifier>ISSN: 1044-0305</identifier><identifier>EISSN: 1879-1123</identifier><identifier>DOI: 10.1016/j.jasms.2006.08.015</identifier><identifier>PMID: 17005416</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Analytical, structural and metabolic biochemistry ; Animals ; Biological and medical sciences ; Brain ; Brain Chemistry ; Cerebellum - chemistry ; Fundamental and applied biological sciences. Psychology ; Glycerolipids, phospholipids ; Glycerophospholipids - chemistry ; Head ; Ionization ; Ions ; Lipids ; Male ; Mass spectrometry ; Neurological diseases ; Other biological molecules ; Rats ; Rats, Sprague-Dawley ; Receptors ; Signal transduction ; Signaling ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods ; Sphingolipids ; Structural analysis ; Sulfoglycosphingolipids - chemistry</subject><ispartof>Journal of the American Society for Mass Spectrometry, 2007, Vol.18 (1), p.17-26</ispartof><rights>2007 American Society for Mass Spectrometry</rights><rights>2007 INIST-CNRS</rights><rights>American Society for Mass Spectrometry 2007</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-5c1b7b95b0ad4a667c186e6fe052c7a769100fe4040339278355e423101754c03</citedby><cites>FETCH-LOGICAL-c526t-5c1b7b95b0ad4a667c186e6fe052c7a769100fe4040339278355e423101754c03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18457622$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17005416$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jackson, Shelley N.</creatorcontrib><creatorcontrib>Wang, Hay-Yan J.</creatorcontrib><creatorcontrib>Woods, Amina S.</creatorcontrib><title>In Situ Structural Characterization of Glycerophospholipids and Sulfatides in Brain Tissue Using MALDI-MS/MS</title><title>Journal of the American Society for Mass Spectrometry</title><addtitle>J Am Soc Mass Spectrom</addtitle><description>Lipids are major structural components of biomembranes. Negatively charged species such as phosphatidylinositol, phosphatidylserine, sulfatides, and the zwitterionic phosphatidylethanolamines are major components of the cytoplasmic surface of the cellular membrane lipid bilayer and play a key role in several receptors signaling functions. Lipids are not just involved in metabolic and neurological diseases; negatively charged lipids in particular play crucial roles in physiological events such as signal transduction, receptors, and enzymatic activation, as well as storage and release of therapeutic drugs and toxic chemicals in the body. Due to the importance of their role in signaling, the field of lipidomics has rapidly expanded in recent years. In the present study, direct probing of tissue slices with negative ion mode matrix assisted laser desorption/ionization mass spectrometry was employed to profile the distribution of lipids in the brain. In total, 32 lipid species consisting of phosphatidylethanolamines, phosphatidylglycerol, phosphatidylinositols, phosphatidylserines, and sulfatides were assigned. To confirm the structure of lipid species, MALDI-MS/MS analysis was conducted. Product-ion spectra obtained in negative ion mode allow for the assignment of the head groups and the fatty acid chains for the lipid species.</description><subject>Analytical, structural and metabolic biochemistry</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Brain</subject><subject>Brain Chemistry</subject><subject>Cerebellum - chemistry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glycerolipids, phospholipids</subject><subject>Glycerophospholipids - chemistry</subject><subject>Head</subject><subject>Ionization</subject><subject>Ions</subject><subject>Lipids</subject><subject>Male</subject><subject>Mass spectrometry</subject><subject>Neurological diseases</subject><subject>Other biological molecules</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors</subject><subject>Signal transduction</subject><subject>Signaling</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods</subject><subject>Sphingolipids</subject><subject>Structural analysis</subject><subject>Sulfoglycosphingolipids - chemistry</subject><issn>1044-0305</issn><issn>1879-1123</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNp9kMtu1DAUQC0EoqXwBUjIEmKZ9Dp-ZsGiHUoZaUYs0q4tj3NDHWWSwU6QytfXZUbqjsV9LM596BDykUHJgKnLvuxd2qeyAlAlmBKYfEXOmdF1wVjFX-cehCiAgzwj71LqAZiGWr8lZ7mCFEydk2E90ibMC23muPh5iW6gqwcXnZ8xhr9uDtNIp47eDo8e43R4mFKOIRxCm6gbW9osQ5epFhMNI72OLue7kNKC9D6F8RfdXm2-rYttc7lt3pM3nRsSfjjVC3L__eZu9aPY_Lxdr642hZeVmgvp2U7varkD1wqnlPbMKFQdgqy8dlrVDKBDAQI4ryttuJQoKp6taCk88Avy-bj3EKffC6bZ9tMSx3zSslpyw5kwJlP8SPk4pRSxs4cY9i4-Wgb22bDt7T_D9tmwBWOz4Tz16bR72e2xfZk5Kc3AlxPgkndDF93oQ3rhjJBaVVXmvh45zCb-BIw2-YCjxzZE9LNtp_DfR54AtCSY0A</recordid><startdate>2007</startdate><enddate>2007</enddate><creator>Jackson, Shelley N.</creator><creator>Wang, Hay-Yan J.</creator><creator>Woods, Amina S.</creator><general>Elsevier Inc</general><general>Elsevier Science</general><general>Springer Nature B.V</general><scope>6I.</scope><scope>AAFTH</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FG</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>P5Z</scope><scope>P62</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope></search><sort><creationdate>2007</creationdate><title>In Situ Structural Characterization of Glycerophospholipids and Sulfatides in Brain Tissue Using MALDI-MS/MS</title><author>Jackson, Shelley N. ; Wang, Hay-Yan J. ; Woods, Amina S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-5c1b7b95b0ad4a667c186e6fe052c7a769100fe4040339278355e423101754c03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Analytical, structural and metabolic biochemistry</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Brain</topic><topic>Brain Chemistry</topic><topic>Cerebellum - chemistry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glycerolipids, phospholipids</topic><topic>Glycerophospholipids - chemistry</topic><topic>Head</topic><topic>Ionization</topic><topic>Ions</topic><topic>Lipids</topic><topic>Male</topic><topic>Mass spectrometry</topic><topic>Neurological diseases</topic><topic>Other biological molecules</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors</topic><topic>Signal transduction</topic><topic>Signaling</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods</topic><topic>Sphingolipids</topic><topic>Structural analysis</topic><topic>Sulfoglycosphingolipids - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jackson, Shelley N.</creatorcontrib><creatorcontrib>Wang, Hay-Yan J.</creatorcontrib><creatorcontrib>Woods, Amina S.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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>ProQuest Central (Corporate)</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest advanced technologies & aerospace journals</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><jtitle>Journal of the American Society for Mass Spectrometry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jackson, Shelley N.</au><au>Wang, Hay-Yan J.</au><au>Woods, Amina S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In Situ Structural Characterization of Glycerophospholipids and Sulfatides in Brain Tissue Using MALDI-MS/MS</atitle><jtitle>Journal of the American Society for Mass Spectrometry</jtitle><addtitle>J Am Soc Mass Spectrom</addtitle><date>2007</date><risdate>2007</risdate><volume>18</volume><issue>1</issue><spage>17</spage><epage>26</epage><pages>17-26</pages><issn>1044-0305</issn><eissn>1879-1123</eissn><abstract>Lipids are major structural components of biomembranes. Negatively charged species such as phosphatidylinositol, phosphatidylserine, sulfatides, and the zwitterionic phosphatidylethanolamines are major components of the cytoplasmic surface of the cellular membrane lipid bilayer and play a key role in several receptors signaling functions. Lipids are not just involved in metabolic and neurological diseases; negatively charged lipids in particular play crucial roles in physiological events such as signal transduction, receptors, and enzymatic activation, as well as storage and release of therapeutic drugs and toxic chemicals in the body. Due to the importance of their role in signaling, the field of lipidomics has rapidly expanded in recent years. In the present study, direct probing of tissue slices with negative ion mode matrix assisted laser desorption/ionization mass spectrometry was employed to profile the distribution of lipids in the brain. In total, 32 lipid species consisting of phosphatidylethanolamines, phosphatidylglycerol, phosphatidylinositols, phosphatidylserines, and sulfatides were assigned. To confirm the structure of lipid species, MALDI-MS/MS analysis was conducted. Product-ion spectra obtained in negative ion mode allow for the assignment of the head groups and the fatty acid chains for the lipid species.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>17005416</pmid><doi>10.1016/j.jasms.2006.08.015</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analytical, structural and metabolic biochemistry Animals Biological and medical sciences Brain Brain Chemistry Cerebellum - chemistry Fundamental and applied biological sciences. Psychology Glycerolipids, phospholipids Glycerophospholipids - chemistry Head Ionization Ions Lipids Male Mass spectrometry Neurological diseases Other biological molecules Rats Rats, Sprague-Dawley Receptors Signal transduction Signaling Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods Sphingolipids Structural analysis Sulfoglycosphingolipids - chemistry |
title | In Situ Structural Characterization of Glycerophospholipids and Sulfatides in Brain Tissue Using MALDI-MS/MS |
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