Downs Melanie L, Baumert Joseph L, Taylor Steve L, Mills E N C
Food Allergy Research and Resource Program, Department of Food Science and Technology, University of Nebraska-Lincoln, Lincoln, NE, USA; Centre for Respiratory Medicine and Allergy, Respiratory Institute of Inflammation and Repair, Manchester Academic Health Sciences Centre and Manchester Institute of Biotechnology, University of Manchester, Manchester, UK.
Food Allergy Research and Resource Program, Department of Food Science and Technology, University of Nebraska-Lincoln, Lincoln, NE, USA.
J Proteomics. 2016 Jun 16;142:62-9. doi: 10.1016/j.jprot.2016.04.045. Epub 2016 May 3.
Thermal processing of allergenic foods can induce changes in the foods' constituent allergens, but the effects of heat treatment are poorly defined. Like other commonly allergenic tree nuts, walnuts often undergo heat treatment (e.g. roasting or baking) prior to consumption. This study evaluated the changes in solubility and detectability of allergens from roasted walnuts using tandem mass spectrometry methods. Walnuts were roasted (132°C or 180°C for 5, 10, or 20min) and prepared for LC-MS/MS using sequential or simultaneous extraction and tryptic digestion protocols. The LC-MS/MS data analysis incorporated label-free quantification of relevant allergens and Maillard adduct screening. In some proteins (2S albumin, LTP, and the 7S globulin N-terminal region) minor changes in relative abundance were observed following roasting. The mature 7S and 11S globulins, however, showed significantly increased detection following roasting at 180°C for 20min when using the simultaneous extraction/digestion protocol, possibly due to increased digestibility of the proteins. The results of this study indicate that individual walnut allergens respond differently to thermal processing, and the detection of these proteins by LC-MS/MS is dependent on the protein in question, its susceptibility to proteolytic digestion, the degree of thermal processing, and the sample preparation methodology.
Understanding the behavior of food allergens in the context of relevant food matrices is critical for both food allergen management and for elucidating matrix and processing-associated factors influencing protein allergenicity. The use of mass spectrometry to identify food allergens and detect allergenic food residues has been increasingly developed due to the advantages associated with the direct, sequence-level analysis possible with MS. To date, however, few studies have implemented MS technology to analyze the effects of thermal processing on allergenic food proteins. The MS analysis results presented in this study revealed not only information about the molecular-level effects of roasting on walnut allergens but also data pertinent to the development of MS-based detection methods for walnut residues in food products.
对致敏性食品进行热处理会导致食品中的致敏原成分发生变化,但热处理的效果尚不明确。与其他常见的致敏性坚果一样,核桃在食用前通常会经过热处理(如烘烤)。本研究使用串联质谱法评估了烤核桃中过敏原的溶解度和可检测性变化。将核桃进行烘烤(132°C或180°C,持续5、10或20分钟),并采用顺序或同时提取及胰蛋白酶消化方案制备用于液相色谱-串联质谱分析的样品。液相色谱-串联质谱数据分析包括对相关过敏原的无标记定量和美拉德加合物筛选。在一些蛋白质(2S白蛋白、脂质转移蛋白和7S球蛋白N端区域)中,烘烤后相对丰度有微小变化。然而,当使用同时提取/消化方案时,成熟的7S和11S球蛋白在180°C烘烤20分钟后检测到的量显著增加,这可能是由于蛋白质的消化率提高。本研究结果表明,核桃中的各个过敏原对热处理的反应不同,通过液相色谱-串联质谱法检测这些蛋白质取决于所讨论的蛋白质、其对蛋白水解消化的敏感性、热处理程度以及样品制备方法。
了解食品过敏原在相关食品基质中的行为对于食品过敏原管理以及阐明影响蛋白质致敏性的基质和加工相关因素至关重要。由于质谱具有直接进行序列水平分析的优势,利用质谱识别食品过敏原和检测致敏性食品残留的技术得到了越来越多的发展。然而,迄今为止,很少有研究采用质谱技术分析热处理对致敏性食品蛋白质的影响。本研究中的质谱分析结果不仅揭示了烘烤对核桃过敏原的分子水平影响信息,还提供了与开发基于质谱的食品中核桃残留检测方法相关的数据。