色谱法
化学
过敏原
假阳性悖论
食品科学
食物过敏原
食品加工
样品制备
牛乳
基质(化学分析)
消化(炼金术)
食品
定量蛋白质组学
定量分析(化学)
葡萄酒
残留物(化学)
食品污染物
蛋白质测序
作者
Yige Wu,Qibin Liang,Rui Chang,Yizhu Chen,Chuncai Liang,Wenkai Cao,Xuan Wu,Sai Fan,Bing Shao,Hui Li
标识
DOI:10.1021/acs.jafc.6c09713
摘要
Abstract Accurate quantification of cow’s milk allergens in processed foods by UPLC-MS/MS is challenged by enzymatic digestion variability and complex matrix effects. β-Casein, a major milk allergen, requires reliable quantification. Herein, we developed a novel method for quantifying bovine β-casein using a recombinant, isotope-labeled, full-length protein (β-casein-I) as an internal standard. With a high isotopic labeling rate and sequence homology to the native analyte, β-casein-I corrects errors from digestion, sample preparation, and MS analysis. The validated method showed excellent linearity from 0.1 to 50 ng/mL. In three processed food matrices, mean recoveries were 89–116% with RSD < 13% at three spiking levels, and LODs were 0.2–0.5 μg/g. Specificity was ensured by simultaneous monitoring of two signature peptides, minimizing false positives from cross-reactivity with goat milk. β-Casein was detected in all 11 commercial samples analyzed. This study provides an accurate, reliable approach for milk allergen quantification, significantly advancing traditional peptide-based methods.
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