Peptide mapping with liquid chromatography using a basic mobile phase
A new peptide mapping with liquid chromatography (LC) using an ammonia-containing basic mobile phase was reported. As compared with a method under a traditional acidic condition with a mobile phase containing trifluoroacetic acid (TFA) or formic acid (FA), the new method exhibited excellent overall...
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Veröffentlicht in: | Journal of Chromatography A 2008-11, Vol.1210 (1), p.76-83 |
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creator | Liu, Hongji Xu, Bi Ray, Manas K. Shahrokh, Zahra |
description | A new peptide mapping with liquid chromatography (LC) using an ammonia-containing basic mobile phase was reported. As compared with a method under a traditional acidic condition with a mobile phase containing trifluoroacetic acid (TFA) or formic acid (FA), the new method exhibited excellent overall performance: it was advantageous over the TFA method in terms of the ultraviolet (UV) and mass spectrometry (MS) sensitivities and the sequence coverage for a tryptic map; it was superior to the FA method in terms of the UV sensitivity, the sequence coverage and the separation capacity. Due to a significant difference in the chromatographic selectivity, several important peptide mapping applications that were sometimes difficult to be conducted previously could now be carried out using the new method. For example, the baseline separation of peptides from the corresponding deamidated products could be achieved with confidence using the new method, a critical pre-requisite for definitive identification and quantification of the deamidation products with LC/MS. No on-column deamidation was observed with the conditions used for the separation. Complementary and confirmative information about a protein could be obtained by running its proteolytic digest under both the basic and acidic conditions. |
doi_str_mv | 10.1016/j.chroma.2008.09.059 |
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As compared with a method under a traditional acidic condition with a mobile phase containing trifluoroacetic acid (TFA) or formic acid (FA), the new method exhibited excellent overall performance: it was advantageous over the TFA method in terms of the ultraviolet (UV) and mass spectrometry (MS) sensitivities and the sequence coverage for a tryptic map; it was superior to the FA method in terms of the UV sensitivity, the sequence coverage and the separation capacity. Due to a significant difference in the chromatographic selectivity, several important peptide mapping applications that were sometimes difficult to be conducted previously could now be carried out using the new method. For example, the baseline separation of peptides from the corresponding deamidated products could be achieved with confidence using the new method, a critical pre-requisite for definitive identification and quantification of the deamidation products with LC/MS. No on-column deamidation was observed with the conditions used for the separation. Complementary and confirmative information about a protein could be obtained by running its proteolytic digest under both the basic and acidic conditions.</description><identifier>ISSN: 0021-9673</identifier><identifier>DOI: 10.1016/j.chroma.2008.09.059</identifier><identifier>PMID: 18838141</identifier><identifier>CODEN: JOCRAM</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Ammonia - chemistry ; Analytical, structural and metabolic biochemistry ; Basic mobile phase ; Biological and medical sciences ; Chromatography, Liquid - methods ; Deamidation analysis ; Formates - chemistry ; Fundamental and applied biological sciences. Psychology ; General aspects, investigation methods ; Mass Spectrometry ; Peptide mapping ; Peptide Mapping - methods ; Proteins ; Reversed phase high-performance liquid chromatography ; Sensitivity and Specificity ; Solvents - chemistry ; Spectrophotometry, Ultraviolet ; Trifluoroacetic Acid - chemistry</subject><ispartof>Journal of Chromatography A, 2008-11, Vol.1210 (1), p.76-83</ispartof><rights>2008 Elsevier B.V.</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c414t-bc2ef0e35ba84b6e75e057cbb63bda3005aee2510d11719667df6956e9984c843</citedby><cites>FETCH-LOGICAL-c414t-bc2ef0e35ba84b6e75e057cbb63bda3005aee2510d11719667df6956e9984c843</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.chroma.2008.09.059$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20813179$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18838141$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Hongji</creatorcontrib><creatorcontrib>Xu, Bi</creatorcontrib><creatorcontrib>Ray, Manas K.</creatorcontrib><creatorcontrib>Shahrokh, Zahra</creatorcontrib><title>Peptide mapping with liquid chromatography using a basic mobile phase</title><title>Journal of Chromatography A</title><addtitle>J Chromatogr A</addtitle><description>A new peptide mapping with liquid chromatography (LC) using an ammonia-containing basic mobile phase was reported. As compared with a method under a traditional acidic condition with a mobile phase containing trifluoroacetic acid (TFA) or formic acid (FA), the new method exhibited excellent overall performance: it was advantageous over the TFA method in terms of the ultraviolet (UV) and mass spectrometry (MS) sensitivities and the sequence coverage for a tryptic map; it was superior to the FA method in terms of the UV sensitivity, the sequence coverage and the separation capacity. Due to a significant difference in the chromatographic selectivity, several important peptide mapping applications that were sometimes difficult to be conducted previously could now be carried out using the new method. For example, the baseline separation of peptides from the corresponding deamidated products could be achieved with confidence using the new method, a critical pre-requisite for definitive identification and quantification of the deamidation products with LC/MS. No on-column deamidation was observed with the conditions used for the separation. Complementary and confirmative information about a protein could be obtained by running its proteolytic digest under both the basic and acidic conditions.</description><subject>Ammonia - chemistry</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>Basic mobile phase</subject><subject>Biological and medical sciences</subject><subject>Chromatography, Liquid - methods</subject><subject>Deamidation analysis</subject><subject>Formates - chemistry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General aspects, investigation methods</subject><subject>Mass Spectrometry</subject><subject>Peptide mapping</subject><subject>Peptide Mapping - methods</subject><subject>Proteins</subject><subject>Reversed phase high-performance liquid chromatography</subject><subject>Sensitivity and Specificity</subject><subject>Solvents - chemistry</subject><subject>Spectrophotometry, Ultraviolet</subject><subject>Trifluoroacetic Acid - chemistry</subject><issn>0021-9673</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1P3DAQQH2gAgr8A9TmQm-bziTx16USQvRDQgIJOFu2M9n1KtkEO6Hi33fTrNobp7m8eZp5jF0i5Agovm5zv4l9Z_MCQOWgc-D6iJ0CFLjSQpYn7GNKWwCUIItjdoJKlQorPGW3DzSMoaass8MQduvsdxg3WRteplBni3Ts19EOm7dsSjNgM2dT8FnXu9BSNmxsonP2obFtoovDPGPP32-fbn6u7u5__Lq5vlv5Cqtx5XxBDVDJnVWVEyQ5AZfeOVG62pYA3BIVHKFGlKiFkHUjNBektaq8qsoz9mXxDrF_mSiNpgvJU9vaHfVTMkILXXGu92C1gD72KUVqzBBDZ-ObQTBzMrM1y3dmTmZAG_i79ungn1xH9f-lQ689cHUAbPK2baLd-ZD-cQUoLFHOos8L19je2HXcM8-PBWAJyKUs1Gz6thC07_UaKJrkA-081SGSH03dh_dv_QPXy5bq</recordid><startdate>20081107</startdate><enddate>20081107</enddate><creator>Liu, Hongji</creator><creator>Xu, Bi</creator><creator>Ray, Manas K.</creator><creator>Shahrokh, Zahra</creator><general>Elsevier B.V</general><general>Amsterdam; New York: Elsevier</general><general>Elsevier</general><scope>FBQ</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>7X8</scope></search><sort><creationdate>20081107</creationdate><title>Peptide mapping with liquid chromatography using a basic mobile phase</title><author>Liu, Hongji ; Xu, Bi ; Ray, Manas K. ; Shahrokh, Zahra</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c414t-bc2ef0e35ba84b6e75e057cbb63bda3005aee2510d11719667df6956e9984c843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Ammonia - chemistry</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Basic mobile phase</topic><topic>Biological and medical sciences</topic><topic>Chromatography, Liquid - methods</topic><topic>Deamidation analysis</topic><topic>Formates - chemistry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General aspects, investigation methods</topic><topic>Mass Spectrometry</topic><topic>Peptide mapping</topic><topic>Peptide Mapping - methods</topic><topic>Proteins</topic><topic>Reversed phase high-performance liquid chromatography</topic><topic>Sensitivity and Specificity</topic><topic>Solvents - chemistry</topic><topic>Spectrophotometry, Ultraviolet</topic><topic>Trifluoroacetic Acid - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Hongji</creatorcontrib><creatorcontrib>Xu, Bi</creatorcontrib><creatorcontrib>Ray, Manas K.</creatorcontrib><creatorcontrib>Shahrokh, Zahra</creatorcontrib><collection>AGRIS</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>MEDLINE - Academic</collection><jtitle>Journal of Chromatography A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Hongji</au><au>Xu, Bi</au><au>Ray, Manas K.</au><au>Shahrokh, Zahra</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Peptide mapping with liquid chromatography using a basic mobile phase</atitle><jtitle>Journal of Chromatography A</jtitle><addtitle>J Chromatogr A</addtitle><date>2008-11-07</date><risdate>2008</risdate><volume>1210</volume><issue>1</issue><spage>76</spage><epage>83</epage><pages>76-83</pages><issn>0021-9673</issn><coden>JOCRAM</coden><abstract>A new peptide mapping with liquid chromatography (LC) using an ammonia-containing basic mobile phase was reported. As compared with a method under a traditional acidic condition with a mobile phase containing trifluoroacetic acid (TFA) or formic acid (FA), the new method exhibited excellent overall performance: it was advantageous over the TFA method in terms of the ultraviolet (UV) and mass spectrometry (MS) sensitivities and the sequence coverage for a tryptic map; it was superior to the FA method in terms of the UV sensitivity, the sequence coverage and the separation capacity. Due to a significant difference in the chromatographic selectivity, several important peptide mapping applications that were sometimes difficult to be conducted previously could now be carried out using the new method. For example, the baseline separation of peptides from the corresponding deamidated products could be achieved with confidence using the new method, a critical pre-requisite for definitive identification and quantification of the deamidation products with LC/MS. No on-column deamidation was observed with the conditions used for the separation. Complementary and confirmative information about a protein could be obtained by running its proteolytic digest under both the basic and acidic conditions.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>18838141</pmid><doi>10.1016/j.chroma.2008.09.059</doi><tpages>8</tpages></addata></record> |
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subjects | Ammonia - chemistry Analytical, structural and metabolic biochemistry Basic mobile phase Biological and medical sciences Chromatography, Liquid - methods Deamidation analysis Formates - chemistry Fundamental and applied biological sciences. Psychology General aspects, investigation methods Mass Spectrometry Peptide mapping Peptide Mapping - methods Proteins Reversed phase high-performance liquid chromatography Sensitivity and Specificity Solvents - chemistry Spectrophotometry, Ultraviolet Trifluoroacetic Acid - chemistry |
title | Peptide mapping with liquid chromatography using a basic mobile phase |
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