食品科学 ›› 2020, Vol. 41 ›› Issue (24): 316-324.doi: 10.7506/spkx1002-6630-20190923-278

• 安全检测 • 上一篇    下一篇

超高效液相色谱-串联质谱法检测大豆主要过敏原蛋白

李丽芳,黄文胜,张九凯,王彦波,傅玲琳,韩晓祥,陈颖   

  1. (1.浙江工商大学食品与生物工程学院,浙江 杭州 310018;2.中国检验检疫科学研究院,北京 100176)
  • 出版日期:2020-12-25 发布日期:2020-12-28
  • 基金资助:
    国家科技重大专项(2018ZX08012-001)

Determination of Major Soybean Allergens by Ultra-high Performance Liquid Chromatography-Tandem Mass Spectrometry

LI Lifang, HUANG Wensheng, ZHANG Jiukai, WANG Yanbo, FU Linglin, HAN Xiaoxiang, CHEN Ying   

  1. (1. School of Food Science and Biotechnology, Zhejiang Gongshang University, Hangzhou 310018, China; 2. Chinese Academy of Inspection and Quarantine, Beijing 100176, China)
  • Online:2020-12-25 Published:2020-12-28

摘要: 为准确检测大豆过敏原,筛查验证表征5 类主要大豆过敏原蛋白的特征肽段,建立基于超高效液相色谱-串联质谱技术的大豆主要过敏原检测方法。优化样品总蛋白提取方法,将大豆蛋白经测序级胰蛋白酶酶解后,利用超高效液相色谱-四极杆-飞行时间质谱对酶解产物进行分析,结合Uniprot数据库完成计算机检索,针对性地鉴定24 种大豆样品的11 种主要过敏原(大豆球蛋白的G1、G2、G3、G4和G5亚基、β-伴大豆球蛋白的α’、α和β亚基、Gly m Bd 30K、Gly m Bd 28K及Kunitz型胰蛋白酶抑制剂)的多肽片段,并从中挖掘用以表征各过敏原的肽段,最终得到29 条响应值高、重复性好的适于质谱检测的特征肽段;进一步利用高效液相色谱-三重四极杆质谱多反应监测模式对这些特征肽段进行验证,发现这些肽段的特异性、灵敏度和稳定性均符合质谱检测要求,可为食品中大豆过敏原的全面、准确检测提供一定的理论基础和技术支持。

关键词: 大豆;过敏原;特征肽段;超高效液相色谱-四极杆-飞行时间质谱;高效液相色谱-三重四极杆质谱

Abstract: In order to develop an accurate method to detect the major soybean allergens using ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS), the signature peptides of the five main soybean allergen proteins were selected and verified. Total protein was extracted from samples under optimized conditions, and it was hydrolyzed by sequencing-grade trypsin. The resulting hydrolysate was analyzed by ultra-high performance liquid chromatography-quadrupole-time of flight-mass spectrometry (UPLC-Q-TOF-MS) combined with computer search of the Uniprot database. Targeted identification of peptide fragments of the five major allergens (Glycinin subunits G1, G2, G3, G4 and G5, β-conglycinin α’, α and β subunits, Gly m Bd 30K, Gly m Bd 28K, and Kunitz trypsin inhibitors) in 24 soybean cultivars was performed. Finally a total of 29 signature peptides with high response value and good reproducibility were obtained, and they were verified by high performance liquid chromatography-triple quadrupole mass spectrometry (HPLC-QQQ-MS) in the multiple reaction monitoring (MRM) mode. The results showed that the specificity, sensitivity and stability of these peptides were in line with the requirements of mass spectrometry detection. In conclusion, this study provide a theoretical basis and technical support for the comprehensive and accurate detection of soybean allergens in foods.

Key words: soybean; allergen; signature peptide; ultra-high performance liquid chromatography-quadrupole time of flight-mass spectrometry; high performance liquid chromatography-triple quadrupole mass spectrometry

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