Downs Melanie L, Johnson Philip
University of Nebraska-Lincoln, Department of Food Science and Technology, Food Allergy Research and Resource Program, 1901 North 21st St, Lincoln, NE 68588-6205.
J AOAC Int. 2018 Jan 1;101(1):146-151. doi: 10.5740/jaoacint.17-0404. Epub 2017 Dec 5.
The detection and quantitation of allergens as contaminants in foods using MS is challenging largely due to the requirement to detect proteins in complex, mixed, and often processed matrixes. Such methods necessarily rely on the use of proteotypic peptides as indicators of the presence and amount of allergenic foods. These peptides should represent the allergenic food in question in such a way that their use is both sensitive (no false-negatives) and specific (no false-positives). Choosing such peptides to represent food allergens is beset with issues, including, but not limited to, separated ingredients (e.g., casein and whey), extraction difficulties (particularly from thermally processed foods), and incomplete sequence information, as well as the more common issues associated with protein quantitation in biological samples. Here, we review the workflows that have been used to select peptide targets for food allergen detection. We describe the use and limitations of both in silico-based analyses and experimental methods relying on high-resolution MS. The variation in the way in which target selection is performed highlights a lack of standardization, even around the principles describing what the detection method should achieve. A lack of focus on the food matrixes to which the method will be applied is also apparent during the peptide target selection process. It is hoped that highlighting some of these issues will assist in the generation of MS-based allergen detection methods that will encourage uptake and use by the analytical community at large.
使用质谱法检测和定量食品中作为污染物的过敏原具有挑战性,这主要是因为需要在复杂、混合且通常经过加工的基质中检测蛋白质。此类方法必然依赖于使用蛋白型肽作为致敏性食品存在和含量的指标。这些肽应以既灵敏(无假阴性)又特异(无假阳性)的方式代表所讨论的致敏性食品。选择此类肽来代表食品过敏原存在诸多问题,包括但不限于成分分离(如酪蛋白和乳清)、提取困难(特别是从热处理食品中提取)、序列信息不完整,以及与生物样品中蛋白质定量相关的更常见问题。在此,我们回顾了用于选择食品过敏原检测肽靶标的工作流程。我们描述了基于计算机分析和依赖高分辨率质谱的实验方法的使用及局限性。靶标选择方式的差异凸显了缺乏标准化,甚至在描述检测方法应达到何种目标的原则方面也是如此。在肽靶标选择过程中,对该方法将应用的食品基质缺乏关注也很明显。希望突出这些问题将有助于生成基于质谱的过敏原检测方法,从而促使广大分析界采用和使用这些方法。