Structural resolution of carbohydrate positional and structural isomers based on gas-phase ion mobility-mass spectrometry
This report describes the rapid characterization of positional and structural carbohydrate isomers based on structural separations provided by ion mobility-mass spectrometry (IM-MS). Many of the diseases associated with glycoprotein variation can be more effectively treated with earlier detection su...
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Veröffentlicht in: | Physical chemistry chemical physics : PCCP 2011-02, Vol.13 (6), p.2196-2205 |
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description | This report describes the rapid characterization of positional and structural carbohydrate isomers based on structural separations provided by ion mobility-mass spectrometry (IM-MS). Many of the diseases associated with glycoprotein variation can be more effectively treated with earlier detection substantiating the need for high-throughput methodologies for glycan characterization. This remains particularly difficult due to heterogeneity, branching, and large size of carbohydrate moieties which creates the potential for numerous isobaric positional and structural isomers that are difficult to characterize using conventional MS methods. IM-MS provides rapid (μs to ms) structural separations by IM and subsequent identification by MS which presents a means for characterization of positional and structural carbohydrate isomers. To chart the structural variation observed in IM-MS, the ion-neutral collision cross sections for over 300 carbohydrates are reported. This diversity can also be varied through the utility of using different alkali metals to tune separation selectivity via alkali metal-carbohydrate coordination. Furthermore, the advantages of combining either pre- and/or post-IM fragmentation prior to MS analysis is demonstrated for enhanced confidence in carbohydrate identification. |
doi_str_mv | 10.1039/c0cp01414a |
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Many of the diseases associated with glycoprotein variation can be more effectively treated with earlier detection substantiating the need for high-throughput methodologies for glycan characterization. This remains particularly difficult due to heterogeneity, branching, and large size of carbohydrate moieties which creates the potential for numerous isobaric positional and structural isomers that are difficult to characterize using conventional MS methods. IM-MS provides rapid (μs to ms) structural separations by IM and subsequent identification by MS which presents a means for characterization of positional and structural carbohydrate isomers. To chart the structural variation observed in IM-MS, the ion-neutral collision cross sections for over 300 carbohydrates are reported. This diversity can also be varied through the utility of using different alkali metals to tune separation selectivity via alkali metal-carbohydrate coordination. Furthermore, the advantages of combining either pre- and/or post-IM fragmentation prior to MS analysis is demonstrated for enhanced confidence in carbohydrate identification.</description><identifier>ISSN: 1463-9076</identifier><identifier>EISSN: 1463-9084</identifier><identifier>DOI: 10.1039/c0cp01414a</identifier><identifier>PMID: 21113554</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Alkali metals ; Carbohydrates ; Carbohydrates - chemistry ; Chemistry ; Cross sections ; Exact sciences and technology ; General and physical chemistry ; Heterogeneity ; Ions - chemistry ; Isomers ; Separation ; Spectrometry ; Spectrometry, Mass, Electrospray Ionization ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ; Spectroscopy</subject><ispartof>Physical chemistry chemical physics : PCCP, 2011-02, Vol.13 (6), p.2196-2205</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c348t-ff319d04cde463774959f99b6a9c8a709b3a6d9fbfb153a80a2473b44424957b3</citedby><cites>FETCH-LOGICAL-c348t-ff319d04cde463774959f99b6a9c8a709b3a6d9fbfb153a80a2473b44424957b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23849648$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21113554$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>FENN, Larissa S</creatorcontrib><creatorcontrib>MCLEAN, John A</creatorcontrib><title>Structural resolution of carbohydrate positional and structural isomers based on gas-phase ion mobility-mass spectrometry</title><title>Physical chemistry chemical physics : PCCP</title><addtitle>Phys Chem Chem Phys</addtitle><description>This report describes the rapid characterization of positional and structural carbohydrate isomers based on structural separations provided by ion mobility-mass spectrometry (IM-MS). Many of the diseases associated with glycoprotein variation can be more effectively treated with earlier detection substantiating the need for high-throughput methodologies for glycan characterization. This remains particularly difficult due to heterogeneity, branching, and large size of carbohydrate moieties which creates the potential for numerous isobaric positional and structural isomers that are difficult to characterize using conventional MS methods. IM-MS provides rapid (μs to ms) structural separations by IM and subsequent identification by MS which presents a means for characterization of positional and structural carbohydrate isomers. To chart the structural variation observed in IM-MS, the ion-neutral collision cross sections for over 300 carbohydrates are reported. This diversity can also be varied through the utility of using different alkali metals to tune separation selectivity via alkali metal-carbohydrate coordination. Furthermore, the advantages of combining either pre- and/or post-IM fragmentation prior to MS analysis is demonstrated for enhanced confidence in carbohydrate identification.</description><subject>Alkali metals</subject><subject>Carbohydrates</subject><subject>Carbohydrates - chemistry</subject><subject>Chemistry</subject><subject>Cross sections</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Heterogeneity</subject><subject>Ions - chemistry</subject><subject>Isomers</subject><subject>Separation</subject><subject>Spectrometry</subject><subject>Spectrometry, Mass, Electrospray Ionization</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><subject>Spectroscopy</subject><issn>1463-9076</issn><issn>1463-9084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtLxTAQhYMovjf-AMlGBKGaNOkjS7n4AkFBXZdJmmilvamZdNF_b65edelqZsh3zmQ4hBxxds6ZUBeGmZFxySVskF0uS5EpVsvN374qd8ge4jtjjBdcbJOdnHMuikLukvkphsnEKUBPg0XfT7HzS-odNRC0f5vbANHS0WO3ekgULFuKf6IO_WADUg1oW5qkr4DZ-JYmujIavO76Ls7ZAIgUR2tiSIIY5gOy5aBHe7iu--Tl-up5cZvdP9zcLS7vMyNkHTPnBFctk6a16ZqqkqpQTildgjI1VExpAWWrnHaaFwJqBrmshJZS5gmttNgnp9--Y_Afk8XYDB0a2_ewtH7CRpWiLnOW83_JWtbpL7xkiTz7Jk3wiMG6ZgzdAGFuOGtWmTQLtnj8yuQywcdr20kPtv1Ff0JIwMkaADTQuwBL0-EfJ2qpyrT7EzN3ljc</recordid><startdate>20110214</startdate><enddate>20110214</enddate><creator>FENN, Larissa S</creator><creator>MCLEAN, John A</creator><general>Royal Society of Chemistry</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>7X8</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20110214</creationdate><title>Structural resolution of carbohydrate positional and structural isomers based on gas-phase ion mobility-mass spectrometry</title><author>FENN, Larissa S ; MCLEAN, John A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c348t-ff319d04cde463774959f99b6a9c8a709b3a6d9fbfb153a80a2473b44424957b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Alkali metals</topic><topic>Carbohydrates</topic><topic>Carbohydrates - chemistry</topic><topic>Chemistry</topic><topic>Cross sections</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Heterogeneity</topic><topic>Ions - chemistry</topic><topic>Isomers</topic><topic>Separation</topic><topic>Spectrometry</topic><topic>Spectrometry, Mass, Electrospray Ionization</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</topic><topic>Spectroscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FENN, Larissa S</creatorcontrib><creatorcontrib>MCLEAN, John A</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>MEDLINE - Academic</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Physical chemistry chemical physics : PCCP</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>FENN, Larissa S</au><au>MCLEAN, John A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural resolution of carbohydrate positional and structural isomers based on gas-phase ion mobility-mass spectrometry</atitle><jtitle>Physical chemistry chemical physics : PCCP</jtitle><addtitle>Phys Chem Chem Phys</addtitle><date>2011-02-14</date><risdate>2011</risdate><volume>13</volume><issue>6</issue><spage>2196</spage><epage>2205</epage><pages>2196-2205</pages><issn>1463-9076</issn><eissn>1463-9084</eissn><abstract>This report describes the rapid characterization of positional and structural carbohydrate isomers based on structural separations provided by ion mobility-mass spectrometry (IM-MS). Many of the diseases associated with glycoprotein variation can be more effectively treated with earlier detection substantiating the need for high-throughput methodologies for glycan characterization. This remains particularly difficult due to heterogeneity, branching, and large size of carbohydrate moieties which creates the potential for numerous isobaric positional and structural isomers that are difficult to characterize using conventional MS methods. IM-MS provides rapid (μs to ms) structural separations by IM and subsequent identification by MS which presents a means for characterization of positional and structural carbohydrate isomers. To chart the structural variation observed in IM-MS, the ion-neutral collision cross sections for over 300 carbohydrates are reported. This diversity can also be varied through the utility of using different alkali metals to tune separation selectivity via alkali metal-carbohydrate coordination. Furthermore, the advantages of combining either pre- and/or post-IM fragmentation prior to MS analysis is demonstrated for enhanced confidence in carbohydrate identification.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><pmid>21113554</pmid><doi>10.1039/c0cp01414a</doi><tpages>10</tpages></addata></record> |
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source | MEDLINE; Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Alkali metals Carbohydrates Carbohydrates - chemistry Chemistry Cross sections Exact sciences and technology General and physical chemistry Heterogeneity Ions - chemistry Isomers Separation Spectrometry Spectrometry, Mass, Electrospray Ionization Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization Spectroscopy |
title | Structural resolution of carbohydrate positional and structural isomers based on gas-phase ion mobility-mass spectrometry |
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