Reliable detection of milk allergens in food using a high-resolution, stand-alone mass spectrometer
Reliable methods are needed for detection of allergenic milk proteins in complex food matrixes. The feasibility of an LC/high-resolution MS method for the analysis of milk proteins in a thermally processed model food (incurred cookies) and in white wine spiked, respectively, with milk powder and cas...
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Veröffentlicht in: | Journal of AOAC International 2011-07, Vol.94 (4), p.1034-1042 |
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description | Reliable methods are needed for detection of allergenic milk proteins in complex food matrixes. The feasibility of an LC/high-resolution MS method for the analysis of milk proteins in a thermally processed model food (incurred cookies) and in white wine spiked, respectively, with milk powder and caseinate is described. Detection of milk proteins was based on the identification of unique peptides in the tryptic digests of cookie/wine extracts using an RP-HPLC separation coupled to an Exactive nonhybrid mass spectrometer using Orbitrap technology. The extremely high mass accuracy and resolution provided by the Orbitrap analyzer allowed a fast preliminary identification of four previously proposed peptide markers of caseins using only accurate values of the m/z of their ions. No interference was observed, despite the complexity of the analyzed matrixes. Moreover, the availability of a high- energy, collisionally activated dissociation cell integrated in the mass spectrometer enabled acquisition of peptide MS/MS-like spectra through post-source fragmentation. Confirmation of peptide marker identity could then be achieved by a comparison between experimental and predicted product ions. The described method shows the great potential of Orbitrap MS as a reliable technique in the field of protein allergen detection once the peptide markers are identified. |
doi_str_mv | 10.1093/jaoac/94.4.1034 |
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The feasibility of an LC/high-resolution MS method for the analysis of milk proteins in a thermally processed model food (incurred cookies) and in white wine spiked, respectively, with milk powder and caseinate is described. Detection of milk proteins was based on the identification of unique peptides in the tryptic digests of cookie/wine extracts using an RP-HPLC separation coupled to an Exactive nonhybrid mass spectrometer using Orbitrap technology. The extremely high mass accuracy and resolution provided by the Orbitrap analyzer allowed a fast preliminary identification of four previously proposed peptide markers of caseins using only accurate values of the m/z of their ions. No interference was observed, despite the complexity of the analyzed matrixes. Moreover, the availability of a high- energy, collisionally activated dissociation cell integrated in the mass spectrometer enabled acquisition of peptide MS/MS-like spectra through post-source fragmentation. Confirmation of peptide marker identity could then be achieved by a comparison between experimental and predicted product ions. The described method shows the great potential of Orbitrap MS as a reliable technique in the field of protein allergen detection once the peptide markers are identified.</description><identifier>ISSN: 1060-3271</identifier><identifier>EISSN: 1944-7922</identifier><identifier>DOI: 10.1093/jaoac/94.4.1034</identifier><identifier>PMID: 21919336</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Allergens ; Allergens - analysis ; Animals ; Chemical properties ; Composition ; Food Analysis - instrumentation ; Food Analysis - methods ; Identification and classification ; Liquid chromatography ; Mass spectrometry ; Mass Spectrometry - instrumentation ; Mass Spectrometry - methods ; Methods ; Milk ; Milk - chemistry ; Physiological aspects ; Reproducibility of Results</subject><ispartof>Journal of AOAC International, 2011-07, Vol.94 (4), p.1034-1042</ispartof><rights>COPYRIGHT 2011 Oxford University Press</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-e23f10c025ae407ec196503b6b6b59d2d9e629ed9054bf942e4ca68a33824b303</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21919336$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Monaci, Linda</creatorcontrib><creatorcontrib>Losito, Ilario</creatorcontrib><creatorcontrib>Palmisano, Francesco</creatorcontrib><creatorcontrib>Visconti, Angelo</creatorcontrib><title>Reliable detection of milk allergens in food using a high-resolution, stand-alone mass spectrometer</title><title>Journal of AOAC International</title><addtitle>J AOAC Int</addtitle><description>Reliable methods are needed for detection of allergenic milk proteins in complex food matrixes. The feasibility of an LC/high-resolution MS method for the analysis of milk proteins in a thermally processed model food (incurred cookies) and in white wine spiked, respectively, with milk powder and caseinate is described. Detection of milk proteins was based on the identification of unique peptides in the tryptic digests of cookie/wine extracts using an RP-HPLC separation coupled to an Exactive nonhybrid mass spectrometer using Orbitrap technology. The extremely high mass accuracy and resolution provided by the Orbitrap analyzer allowed a fast preliminary identification of four previously proposed peptide markers of caseins using only accurate values of the m/z of their ions. No interference was observed, despite the complexity of the analyzed matrixes. Moreover, the availability of a high- energy, collisionally activated dissociation cell integrated in the mass spectrometer enabled acquisition of peptide MS/MS-like spectra through post-source fragmentation. Confirmation of peptide marker identity could then be achieved by a comparison between experimental and predicted product ions. The described method shows the great potential of Orbitrap MS as a reliable technique in the field of protein allergen detection once the peptide markers are identified.</description><subject>Allergens</subject><subject>Allergens - analysis</subject><subject>Animals</subject><subject>Chemical properties</subject><subject>Composition</subject><subject>Food Analysis - instrumentation</subject><subject>Food Analysis - methods</subject><subject>Identification and classification</subject><subject>Liquid chromatography</subject><subject>Mass spectrometry</subject><subject>Mass Spectrometry - instrumentation</subject><subject>Mass Spectrometry - methods</subject><subject>Methods</subject><subject>Milk</subject><subject>Milk - chemistry</subject><subject>Physiological aspects</subject><subject>Reproducibility of Results</subject><issn>1060-3271</issn><issn>1944-7922</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkUtLxDAUhYMozvhYu5OACzd2Jq-2k-Uw-AJBEF2HNL0dM6bNmLQL_72po4Igd5Hk8p3DzT0InVEyo0Ty-UZ7beZSzER6c7GHplQKkZWSsf10JwXJOCvpBB3FuCFE0IKwQzRhVFLJeTFF5gmc1ZUDXEMPpre-w77BrXVvWDsHYQ1dxLbDjfc1HqLt1ljjV7t-zQJE74ZRcYVjr7s60853gFsdI47bZBZ8m0zDCTpotItw-n0eo5eb6-fVXfbweHu_Wj5kRpSkz4DxhhJDWK5BkBIMlUVOeFWkymXNagkFk1BLkouqkYKBMLpYaM4XTFSc8GN0ufPdBv8-QOxVa6MB53QHfohqIUlR5rmUibzYkWvtQNmu8X3QZqTVkiUmrScf_Wb_UKlqaK1JX21s6v8RzHcCE3yMARq1DbbV4UNRosa81FdeSgol1JhXUpx_jzxULdS__E9A_BMEypC7</recordid><startdate>20110701</startdate><enddate>20110701</enddate><creator>Monaci, Linda</creator><creator>Losito, Ilario</creator><creator>Palmisano, Francesco</creator><creator>Visconti, Angelo</creator><general>Oxford University Press</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>20110701</creationdate><title>Reliable detection of milk allergens in food using a high-resolution, stand-alone mass spectrometer</title><author>Monaci, Linda ; Losito, Ilario ; Palmisano, Francesco ; Visconti, Angelo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-e23f10c025ae407ec196503b6b6b59d2d9e629ed9054bf942e4ca68a33824b303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Allergens</topic><topic>Allergens - analysis</topic><topic>Animals</topic><topic>Chemical properties</topic><topic>Composition</topic><topic>Food Analysis - instrumentation</topic><topic>Food Analysis - methods</topic><topic>Identification and classification</topic><topic>Liquid chromatography</topic><topic>Mass spectrometry</topic><topic>Mass Spectrometry - instrumentation</topic><topic>Mass Spectrometry - methods</topic><topic>Methods</topic><topic>Milk</topic><topic>Milk - chemistry</topic><topic>Physiological aspects</topic><topic>Reproducibility of Results</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Monaci, Linda</creatorcontrib><creatorcontrib>Losito, Ilario</creatorcontrib><creatorcontrib>Palmisano, Francesco</creatorcontrib><creatorcontrib>Visconti, Angelo</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 AOAC International</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Monaci, Linda</au><au>Losito, Ilario</au><au>Palmisano, Francesco</au><au>Visconti, Angelo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reliable detection of milk allergens in food using a high-resolution, stand-alone mass spectrometer</atitle><jtitle>Journal of AOAC International</jtitle><addtitle>J AOAC Int</addtitle><date>2011-07-01</date><risdate>2011</risdate><volume>94</volume><issue>4</issue><spage>1034</spage><epage>1042</epage><pages>1034-1042</pages><issn>1060-3271</issn><eissn>1944-7922</eissn><abstract>Reliable methods are needed for detection of allergenic milk proteins in complex food matrixes. The feasibility of an LC/high-resolution MS method for the analysis of milk proteins in a thermally processed model food (incurred cookies) and in white wine spiked, respectively, with milk powder and caseinate is described. Detection of milk proteins was based on the identification of unique peptides in the tryptic digests of cookie/wine extracts using an RP-HPLC separation coupled to an Exactive nonhybrid mass spectrometer using Orbitrap technology. The extremely high mass accuracy and resolution provided by the Orbitrap analyzer allowed a fast preliminary identification of four previously proposed peptide markers of caseins using only accurate values of the m/z of their ions. No interference was observed, despite the complexity of the analyzed matrixes. Moreover, the availability of a high- energy, collisionally activated dissociation cell integrated in the mass spectrometer enabled acquisition of peptide MS/MS-like spectra through post-source fragmentation. Confirmation of peptide marker identity could then be achieved by a comparison between experimental and predicted product ions. The described method shows the great potential of Orbitrap MS as a reliable technique in the field of protein allergen detection once the peptide markers are identified.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>21919336</pmid><doi>10.1093/jaoac/94.4.1034</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE |
subjects | Allergens Allergens - analysis Animals Chemical properties Composition Food Analysis - instrumentation Food Analysis - methods Identification and classification Liquid chromatography Mass spectrometry Mass Spectrometry - instrumentation Mass Spectrometry - methods Methods Milk Milk - chemistry Physiological aspects Reproducibility of Results |
title | Reliable detection of milk allergens in food using a high-resolution, stand-alone mass spectrometer |
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