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Quantitative Proteomic Profiling of Peanut Allergens in Food Ingredients Used for Oral Food Challenges

机译:用于口服食品挑战的食品成分中花生过敏原的定量蛋白质组分析

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Profiling allergens in complex food ingredients used in oral food challenges and immunotherapy is crucial for regulatory acceptance. Mass spectrometry based analysis employing data-independent acquisition coupled with ion mobility mass spectrometry mass spectrometry (DIA-IM-MS) was used to investigate the allergen composition of raw peanuts and roasted peanut flour ingredients used in challenge meals. This comprehensive qualitative and quantitative analysis using label free approaches identified and quantified 123 unique protein accessions. Semiquantitative analysis indicated that allergens Ara h 1 and Ara h 3 were the most abundant proteins and present in approximately equal amounts and were extracted in reduced amounts from roasted peanut flours. The clinically significant allergens Am h 2 and 6 were less abundant, but relative quantification was unaffected by roasting. Ara h 5 was undetectable in any peanut sample, while the Bet v 1 homologue Ara h 8 and the lipid transfer protein allergen, Ara h 9, were detected in low abundance. The oleosin allergens, Ara h 10 and 11, were moderately abundant in the raw peanuts but were 100-fold less abundant in the defatted roasted peanut flour than the major allergens Ara h 1, 3, 2, and 6. Certain isoforms of the major allergens dominated the profile. The relative quantitation of the major peanut allergens showed little variation between different batches of roasted peanut flour. These data will support future development of targeted approaches for absolute quantification of peanut allergens which can be applied to both food ingredients used in clinical studies and extracts used for skin testing and to identify trace levels of allergens in foods.
机译:对用于口服食品挑战和免疫疗法的复杂食品成分中的过敏原进行分析对于法规接受至关重要。基于质谱的分析采用与数据无关的采集结合离子迁移质谱法(DIA-IM-MS),用于研究用于挑战餐的生花生和烤花生粉成分的过敏原成分。使用无标记方法进行的全面定性和定量分析,鉴定并定量了123种独特的蛋白质。半定量分析表明,过敏原Ara h 1和Ara h 3是最丰富的蛋白质,并且以大约相等的量存在,并且从烤花生粉中以减少的量提取。临床上重要的过敏原Am h 2和6含量较低,但相对定量不受焙烧的影响。在任何花生样品中均未检测到Ara h 5,而以低丰度检测到Bet v 1同源Ara h 8和脂质转移蛋白过敏原Ara h 9。生花生中的油质蛋白过敏原Ara h 10和11适度丰富,但脱脂烤花生粉中的油质蛋白过敏原含量比主要变应原Ara h 1、3、2和6低100倍。过敏原占主导地位。主要花生过敏原的相对定量显示,不同批次的烤花生粉之间变化不大。这些数据将支持未来对花生过敏原进行绝对定量的靶向方法的开发,该方法既可应用于临床研究中使用的食品成分,也可用于皮肤测试的提取物,并用于识别食品中的痕量过敏原。

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