Institute of Food Chemistry, Westfälische Wilhelms-Universität Münster, Corrensstraße 45, Münster 48149, Germany.
Institute of Biochemistry and Technical Biochemistry, Department of Food Chemistry, University of Stuttgart, Allmandring 5b, Stuttgart 70569, Germany.
J Proteomics. 2019 Mar 30;196:131-140. doi: 10.1016/j.jprot.2018.11.002. Epub 2018 Nov 5.
Food allergies are a growing worldwide concern and the contamination of products with food allergens represents a significant health risk to allergic consumers. With the introduction of reference doses, quantitative methods are needed for the monitoring of allergen levels, and the potential of LC-MS/MS is of hugely growing interest. In this study, we demonstrate that relevant food matrices (bakery products and chocolates) and thermal food processing substantially influence the quantification of 18 marker peptides from various nut and peanut allergens via targeted proteomics. In addition, we characterize the individual release kinetics of marker peptides and provide examples for metastable marker peptide candidates. Matrix recovery rates overall ranged between 15 and 250% with the observed variation being linked to the individual peptide structure as well as to specific matrix interferences. In contrast, thermal processing considerably influences the detectability of allergens on the protein level as different marker peptides from the identical parent allergen are similarly affected, leading to a loss in signal of up to 83% in extreme cases after a 45-min simulated baking. Provided data are finally used for evaluation of different calibrators as well as the overall potential and challenges of LC-MS for the absolute quantification of food allergens. SIGNIFICANCE: With the scientific discussion moving towards a risk-based management of food allergens, including the establishment of threshold doses, robust methods for the absolute quantification of allergens in food samples are urgently needed. Because the currently used antibody- and DNA-based technologies show severe limitations in terms of specificity and reproducibility, LC-MS has emerged as a promising alternative. Its application to absolute quantification, however, first requires an understanding of the various impacts that affect quantification results, including different food matrices, sample preparation, and thermal processing of foodstuffs. Knowledge of these factors, which are assessed as part of a comprehensive survey in this study, is also an important prerequisite to evaluate means of calibration for an LC-MS-based quantification of food allergens.
食物过敏是一个日益严重的全球性问题,食物过敏原的产品污染对过敏消费者构成了重大健康风险。随着参考剂量的引入,需要定量方法来监测过敏原水平,而 LC-MS/MS 的潜力也引起了极大的关注。在这项研究中,我们证明了相关的食物基质(烘焙产品和巧克力)和热食品加工会极大地影响通过靶向蛋白质组学对来自各种坚果和花生过敏原的 18 个标记肽进行定量。此外,我们还描述了标记肽的个体释放动力学,并提供了亚稳标记肽候选物的示例。总体而言,基质回收率在 15%到 250%之间,观察到的变化与个别肽结构以及特定的基质干扰有关。相比之下,热加工会极大地影响过敏原在蛋白质水平上的可检测性,因为来自相同母体过敏原的不同标记肽会受到类似的影响,导致在极端情况下,经过 45 分钟的模拟烘焙后,信号损失高达 83%。最终提供的数据用于评估不同的校准物以及 LC-MS 用于绝对定量食物过敏原的整体潜力和挑战。意义:随着科学讨论朝着基于风险的食物过敏原管理方向发展,包括建立阈值剂量,因此迫切需要用于食物样品中过敏原绝对定量的稳健方法。由于目前使用的基于抗体和 DNA 的技术在特异性和重现性方面存在严重的局限性,LC-MS 已成为一种很有前途的替代方法。然而,将其应用于绝对定量首先需要了解影响定量结果的各种因素,包括不同的食物基质、样品制备和食物的热加工。本研究作为全面调查的一部分,对这些因素进行了评估,了解这些因素是评估基于 LC-MS 的食物过敏原定量校准手段的重要前提。