24-Hour Lock Mass Protection
The positive role and application of highly accurate mass measurements in proteomics is well documented. The new generation of hybrid FTMS and Q-TOF instruments, including the LTQ-Orbitrap (OT), is remarkable in their ability to routinely produce single-digit to subppm statistical mass accuracy whil...
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Veröffentlicht in: | Journal of proteome research 2011-02, Vol.10 (2), p.880-885 |
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creator | Lee, Kimberly A Farnsworth, Chris Yu, Wen Bonilla, Leo E |
description | The positive role and application of highly accurate mass measurements in proteomics is well documented. The new generation of hybrid FTMS and Q-TOF instruments, including the LTQ-Orbitrap (OT), is remarkable in their ability to routinely produce single-digit to subppm statistical mass accuracy while maintaining high analytical sensitivity. The use of mass calibrants (lock masses) to reduce the systematic error of mass-to-charge measurements has also been reported and, in some cases, incorporated in the instrument control software by the instrument manufacturers. We evaluated the use of one such calibrant in the OT (e.g., polydimethylcyclosiloxane, PCM) to study its impact on the rate of phosphopeptide annotation and found it to lack robustness under normal laboratory conditions. Therefore, we devised a strategy to improve its performance by increasing the external abundance of calibrant molecules in laboratory air. This resulted in a more robust performance of the preprogrammed lock mass recalibration feature as evidenced by improvements in both statistical mass accuracy and peptide annotation rates. |
doi_str_mv | 10.1021/pr100780b |
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This resulted in a more robust performance of the preprogrammed lock mass recalibration feature as evidenced by improvements in both statistical mass accuracy and peptide annotation rates.</description><identifier>ISSN: 1535-3893</identifier><identifier>EISSN: 1535-3907</identifier><identifier>DOI: 10.1021/pr100780b</identifier><identifier>PMID: 21133379</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Calibration ; Deodorants - chemistry ; Dimethylpolysiloxanes - chemistry ; Humans ; Jurkat Cells ; Mass Spectrometry - methods ; Mass Spectrometry - standards ; Molecular Weight ; Peptide Fragments - chemistry ; Phosphopeptides - chemistry ; Proteomics - methods ; Proteomics - standards</subject><ispartof>Journal of proteome research, 2011-02, Vol.10 (2), p.880-885</ispartof><rights>Copyright © 2010 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a314t-c8e4d2e15b69891aa7496f7a457b8758a08397c33c4816a570dae3fcdb3ba03c3</citedby><cites>FETCH-LOGICAL-a314t-c8e4d2e15b69891aa7496f7a457b8758a08397c33c4816a570dae3fcdb3ba03c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/pr100780b$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/pr100780b$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,777,781,2752,27057,27905,27906,56719,56769</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21133379$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Kimberly A</creatorcontrib><creatorcontrib>Farnsworth, Chris</creatorcontrib><creatorcontrib>Yu, Wen</creatorcontrib><creatorcontrib>Bonilla, Leo E</creatorcontrib><title>24-Hour Lock Mass Protection</title><title>Journal of proteome research</title><addtitle>J. Proteome Res</addtitle><description>The positive role and application of highly accurate mass measurements in proteomics is well documented. The new generation of hybrid FTMS and Q-TOF instruments, including the LTQ-Orbitrap (OT), is remarkable in their ability to routinely produce single-digit to subppm statistical mass accuracy while maintaining high analytical sensitivity. The use of mass calibrants (lock masses) to reduce the systematic error of mass-to-charge measurements has also been reported and, in some cases, incorporated in the instrument control software by the instrument manufacturers. We evaluated the use of one such calibrant in the OT (e.g., polydimethylcyclosiloxane, PCM) to study its impact on the rate of phosphopeptide annotation and found it to lack robustness under normal laboratory conditions. Therefore, we devised a strategy to improve its performance by increasing the external abundance of calibrant molecules in laboratory air. This resulted in a more robust performance of the preprogrammed lock mass recalibration feature as evidenced by improvements in both statistical mass accuracy and peptide annotation rates.</description><subject>Calibration</subject><subject>Deodorants - chemistry</subject><subject>Dimethylpolysiloxanes - chemistry</subject><subject>Humans</subject><subject>Jurkat Cells</subject><subject>Mass Spectrometry - methods</subject><subject>Mass Spectrometry - standards</subject><subject>Molecular Weight</subject><subject>Peptide Fragments - chemistry</subject><subject>Phosphopeptides - chemistry</subject><subject>Proteomics - methods</subject><subject>Proteomics - standards</subject><issn>1535-3893</issn><issn>1535-3907</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkL9PwzAQhS0EoqUwsCPUBSGGwF3Oqe2xqoAiFcEAs3VxHKmlrYudDPz3BPXHxHQ3fPr03hPiEuEeIceHTUQApaE8En0sqMjIgDre_9pQT5yltADAQgGdil6OSETK9MVVLrNpaONwFtzX8JVTGr7H0HjXzMP6XJzUvEz-YncH4vPp8WMyzWZvzy-T8SxjQtlkTntZ5R6LcmS0QWYlzahWLAtValVoBk1GOSInNY64y1Cxp9pVJZUM5GggbrfeTQzfrU-NXc2T88slr31ok9XSSMpzgo6825IuhpSir-0mzlccfyyC_dvCHrbo2OudtS1XvjqQ-_IdcLMF2CW76EZYdyX_Ef0Cm-9iYg</recordid><startdate>20110204</startdate><enddate>20110204</enddate><creator>Lee, Kimberly A</creator><creator>Farnsworth, Chris</creator><creator>Yu, Wen</creator><creator>Bonilla, Leo E</creator><general>American Chemical Society</general><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>20110204</creationdate><title>24-Hour Lock Mass Protection</title><author>Lee, Kimberly A ; Farnsworth, Chris ; Yu, Wen ; Bonilla, Leo E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a314t-c8e4d2e15b69891aa7496f7a457b8758a08397c33c4816a570dae3fcdb3ba03c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Calibration</topic><topic>Deodorants - chemistry</topic><topic>Dimethylpolysiloxanes - chemistry</topic><topic>Humans</topic><topic>Jurkat Cells</topic><topic>Mass Spectrometry - methods</topic><topic>Mass Spectrometry - standards</topic><topic>Molecular Weight</topic><topic>Peptide Fragments - chemistry</topic><topic>Phosphopeptides - chemistry</topic><topic>Proteomics - methods</topic><topic>Proteomics - standards</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Kimberly A</creatorcontrib><creatorcontrib>Farnsworth, Chris</creatorcontrib><creatorcontrib>Yu, Wen</creatorcontrib><creatorcontrib>Bonilla, Leo E</creatorcontrib><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>Journal of proteome research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Kimberly A</au><au>Farnsworth, Chris</au><au>Yu, Wen</au><au>Bonilla, Leo E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>24-Hour Lock Mass Protection</atitle><jtitle>Journal of proteome research</jtitle><addtitle>J. Proteome Res</addtitle><date>2011-02-04</date><risdate>2011</risdate><volume>10</volume><issue>2</issue><spage>880</spage><epage>885</epage><pages>880-885</pages><issn>1535-3893</issn><eissn>1535-3907</eissn><abstract>The positive role and application of highly accurate mass measurements in proteomics is well documented. The new generation of hybrid FTMS and Q-TOF instruments, including the LTQ-Orbitrap (OT), is remarkable in their ability to routinely produce single-digit to subppm statistical mass accuracy while maintaining high analytical sensitivity. The use of mass calibrants (lock masses) to reduce the systematic error of mass-to-charge measurements has also been reported and, in some cases, incorporated in the instrument control software by the instrument manufacturers. We evaluated the use of one such calibrant in the OT (e.g., polydimethylcyclosiloxane, PCM) to study its impact on the rate of phosphopeptide annotation and found it to lack robustness under normal laboratory conditions. Therefore, we devised a strategy to improve its performance by increasing the external abundance of calibrant molecules in laboratory air. This resulted in a more robust performance of the preprogrammed lock mass recalibration feature as evidenced by improvements in both statistical mass accuracy and peptide annotation rates.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>21133379</pmid><doi>10.1021/pr100780b</doi><tpages>6</tpages></addata></record> |
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subjects | Calibration Deodorants - chemistry Dimethylpolysiloxanes - chemistry Humans Jurkat Cells Mass Spectrometry - methods Mass Spectrometry - standards Molecular Weight Peptide Fragments - chemistry Phosphopeptides - chemistry Proteomics - methods Proteomics - standards |
title | 24-Hour Lock Mass Protection |
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