Secondary ion-molecule reactions in matrix-assisted laser desorption/ionization
Ion‐molecule charge‐ and proton‐transfer reactions in the desorption plume are considered for the case of matrix‐assisted laser desorption/ionization (MALDI) with ultraviolet laser excitation, and it is proposed that they are major determinants of the observed mass spectrum. Specific MALDI phenomena...
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Veröffentlicht in: | Journal of mass spectrometry. 2000-11, Vol.35 (11), p.1237-1245 |
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creator | Knochenmuss, R. Stortelder, A. Breuker, K. Zenobi, R. |
description | Ion‐molecule charge‐ and proton‐transfer reactions in the desorption plume are considered for the case of matrix‐assisted laser desorption/ionization (MALDI) with ultraviolet laser excitation, and it is proposed that they are major determinants of the observed mass spectrum. Specific MALDI phenomena which are discussed include the dominance of singly charged ions and analyte–matrix or analyte–analyte signal suppression. Should any be formed, highly charged products can be reduced by reaction with neutral matrix, yet singly charged ions cannot generally be neutralized in the same manner. Ion suppression effects can also be explained by similar reactions, which in some cases involve interconversion of dissimilar ion types. The plume is proposed often to be more under thermodynamic rather than kinetic control owing to these secondary reactions. UV/MALDI mass spectra should therefore be largely predictable, given sufficient thermodynamic information, and appropriate experimental conditions of sufficient analyte and plume density. Copyright © 2000 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/1096-9888(200011)35:11<1237::AID-JMS74>3.0.CO;2-O |
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Specific MALDI phenomena which are discussed include the dominance of singly charged ions and analyte–matrix or analyte–analyte signal suppression. Should any be formed, highly charged products can be reduced by reaction with neutral matrix, yet singly charged ions cannot generally be neutralized in the same manner. Ion suppression effects can also be explained by similar reactions, which in some cases involve interconversion of dissimilar ion types. The plume is proposed often to be more under thermodynamic rather than kinetic control owing to these secondary reactions. UV/MALDI mass spectra should therefore be largely predictable, given sufficient thermodynamic information, and appropriate experimental conditions of sufficient analyte and plume density. Copyright © 2000 John Wiley & Sons, Ltd.</description><identifier>ISSN: 1076-5174</identifier><identifier>EISSN: 1096-9888</identifier><identifier>DOI: 10.1002/1096-9888(200011)35:11<1237::AID-JMS74>3.0.CO;2-O</identifier><identifier>PMID: 11114080</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Chemistry ; electron transfer ; Exact sciences and technology ; ion-molecule reactions ; Mass spectrometry ; matrix-assisted laser desorption/ionization ; Organic chemistry ; proton transfer ; Reactivity and mechanisms</subject><ispartof>Journal of mass spectrometry., 2000-11, Vol.35 (11), p.1237-1245</ispartof><rights>Copyright © 2000 John Wiley & Sons, Ltd.</rights><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4914-69b95535740e3a293c33f2040c5afe9f49c5c872b0b4ee32e8e64de39ac4b33a3</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%2F1096-9888%28200011%2935%3A11%3C1237%3A%3AAID-JMS74%3E3.0.CO%3B2-O$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F1096-9888%28200011%2935%3A11%3C1237%3A%3AAID-JMS74%3E3.0.CO%3B2-O$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=825899$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11114080$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Knochenmuss, R.</creatorcontrib><creatorcontrib>Stortelder, A.</creatorcontrib><creatorcontrib>Breuker, K.</creatorcontrib><creatorcontrib>Zenobi, R.</creatorcontrib><title>Secondary ion-molecule reactions in matrix-assisted laser desorption/ionization</title><title>Journal of mass spectrometry.</title><addtitle>J. Mass Spectrom</addtitle><description>Ion‐molecule charge‐ and proton‐transfer reactions in the desorption plume are considered for the case of matrix‐assisted laser desorption/ionization (MALDI) with ultraviolet laser excitation, and it is proposed that they are major determinants of the observed mass spectrum. Specific MALDI phenomena which are discussed include the dominance of singly charged ions and analyte–matrix or analyte–analyte signal suppression. Should any be formed, highly charged products can be reduced by reaction with neutral matrix, yet singly charged ions cannot generally be neutralized in the same manner. Ion suppression effects can also be explained by similar reactions, which in some cases involve interconversion of dissimilar ion types. The plume is proposed often to be more under thermodynamic rather than kinetic control owing to these secondary reactions. UV/MALDI mass spectra should therefore be largely predictable, given sufficient thermodynamic information, and appropriate experimental conditions of sufficient analyte and plume density. Copyright © 2000 John Wiley & Sons, Ltd.</description><subject>Chemistry</subject><subject>electron transfer</subject><subject>Exact sciences and technology</subject><subject>ion-molecule reactions</subject><subject>Mass spectrometry</subject><subject>matrix-assisted laser desorption/ionization</subject><subject>Organic chemistry</subject><subject>proton transfer</subject><subject>Reactivity and mechanisms</subject><issn>1076-5174</issn><issn>1096-9888</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqVkUtv1DAURiMEoqXlL6BIbNqFp34m9oAqVVNaWgoRGqDsrhznRgrkMdgzasuvxyGjYcOmlmxfWcef7eMkMYzOGKX8hFGTEaO1PuKUUsaOhZoz9pZxkc_nZ1fn5PrjMpenYkZni-INJ8WTZH-35-lY5xlRLJd7yYsQfsQMY2T2PNljsUmq6X5SLNENfWX9Q9oMPemGFt2mxdSjdeu4EtKmTzu79s09sSE0YY1V2tqAPq0wDH41QiexN7_tWB4mz2rbBny5nQ-Srxfvvizek5vi8mpxdkOcNEySzJRGKaFySVFYboQTouZUUqdsjaaWximnc17SUiIKjhozWaEw1slSCCsOkqMpd-WHXxsMa-ia4LBtbY_DJgDTygiRK8kj-nlCnR9C8FjDyjddfDEwCqNnGJ3B6AwmzyAUxHH0DBA9w1_PIIDCogAORcx8tT1-U3ZY_Uvcio3A6y1gg7Nt7W3vmrDjNFfamEgtJ-quafHhUff637WmhZhKptTxt-53qdb_hCyPTuD20yXcXmTfsmv-HT6IP6iEskM</recordid><startdate>200011</startdate><enddate>200011</enddate><creator>Knochenmuss, R.</creator><creator>Stortelder, A.</creator><creator>Breuker, K.</creator><creator>Zenobi, R.</creator><general>John Wiley & Sons, Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200011</creationdate><title>Secondary ion-molecule reactions in matrix-assisted laser desorption/ionization</title><author>Knochenmuss, R. ; Stortelder, A. ; Breuker, K. ; Zenobi, R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4914-69b95535740e3a293c33f2040c5afe9f49c5c872b0b4ee32e8e64de39ac4b33a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Chemistry</topic><topic>electron transfer</topic><topic>Exact sciences and technology</topic><topic>ion-molecule reactions</topic><topic>Mass spectrometry</topic><topic>matrix-assisted laser desorption/ionization</topic><topic>Organic chemistry</topic><topic>proton transfer</topic><topic>Reactivity and mechanisms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Knochenmuss, R.</creatorcontrib><creatorcontrib>Stortelder, A.</creatorcontrib><creatorcontrib>Breuker, K.</creatorcontrib><creatorcontrib>Zenobi, R.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of mass spectrometry.</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Knochenmuss, R.</au><au>Stortelder, A.</au><au>Breuker, K.</au><au>Zenobi, R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Secondary ion-molecule reactions in matrix-assisted laser desorption/ionization</atitle><jtitle>Journal of mass spectrometry.</jtitle><addtitle>J. Mass Spectrom</addtitle><date>2000-11</date><risdate>2000</risdate><volume>35</volume><issue>11</issue><spage>1237</spage><epage>1245</epage><pages>1237-1245</pages><issn>1076-5174</issn><eissn>1096-9888</eissn><abstract>Ion‐molecule charge‐ and proton‐transfer reactions in the desorption plume are considered for the case of matrix‐assisted laser desorption/ionization (MALDI) with ultraviolet laser excitation, and it is proposed that they are major determinants of the observed mass spectrum. Specific MALDI phenomena which are discussed include the dominance of singly charged ions and analyte–matrix or analyte–analyte signal suppression. Should any be formed, highly charged products can be reduced by reaction with neutral matrix, yet singly charged ions cannot generally be neutralized in the same manner. Ion suppression effects can also be explained by similar reactions, which in some cases involve interconversion of dissimilar ion types. The plume is proposed often to be more under thermodynamic rather than kinetic control owing to these secondary reactions. UV/MALDI mass spectra should therefore be largely predictable, given sufficient thermodynamic information, and appropriate experimental conditions of sufficient analyte and plume density. Copyright © 2000 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>11114080</pmid><doi>10.1002/1096-9888(200011)35:11<1237::AID-JMS74>3.0.CO;2-O</doi><tpages>9</tpages></addata></record> |
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subjects | Chemistry electron transfer Exact sciences and technology ion-molecule reactions Mass spectrometry matrix-assisted laser desorption/ionization Organic chemistry proton transfer Reactivity and mechanisms |
title | Secondary ion-molecule reactions in matrix-assisted laser desorption/ionization |
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