Development of a mass spectrometry immunoassay for unambiguous detection of egg allergen traces in wines
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  • 作者:Rosa Pilolli ; Ravindra Chaudhari…
  • 关键词:Egg allergen ; Wine ; MSIA ; Immunoassay ; Mass spectrometry ; Ovalbumin
  • 刊名:Analytical and Bioanalytical Chemistry
  • 出版年:2017
  • 出版时间:February 2017
  • 年:2017
  • 卷:409
  • 期:6
  • 页码:1581-1589
  • 全文大小:
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Analytical Chemistry; Biochemistry, general; Laboratory Medicine; Characterization and Evaluation of Materials; Food Science; Monitoring/Environmental Analysis;
  • 出版者:Springer Berlin Heidelberg
  • ISSN:1618-2650
  • 卷排序:409
文摘
A mass spectrometry immunoassay (MSIA) specifically designed for the detection of egg allergens in wines is described. MSIA is based on an immunoaffinity enrichment procedure combined with targeted MS/MS detection of selected egg peptide markers. Polyclonal antibodies raised against native ovalbumin, chosen as the target protein tracing for egg powder, were immobilized onto low backpressure monolithic MSIA customized disposable tips. Ovalbumin-free wine samples were fortified with standard protein at different concentrations in the low microgram-per-milliliter range. A simple protocol was devised consisting of a 1:4 dilution of the wine sample with a basic solution for pH adjustment, followed by a semi-automated purification/enrichment step on MSIA customized disposable tips fitted on a multichannel electronic pipette. Among the main figures of merit, LOD and LOQ values as low as 0.01 and 0.03 μg/mL, respectively, and within-day precision of 18% should be noticed. Noteworthy, the developed assay outperformed current MS-based methods for the detection of allergenic protein in wine matrices, thanks to the immunoaffinity enrichment. In addition, compared to other immunoassays, the present approach boasts the unquestionable advantage of providing an unambiguous identification of the target protein by simultaneous detection of three unique peptide markers each giving three specific MS/MS transitions.

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