Development of a competitive ELISA based on estrogen receptor and weak competitive molecule for the screening of potential estrogens in foods

被引:18
作者
Wang, Ying [1 ,2 ]
Wang, Minglu [1 ]
Zhou, Li [3 ]
Geng, Xiangye [1 ]
Xu, Zhixiang [2 ]
Zhang, Hongyan [1 ]
机构
[1] Shandong Normal Univ, Coll Life Sci, Shandong Prov Key Lab Anim Resistance Biol, Key Lab Food Nutr & Safety, Jinan 250014, Peoples R China
[2] Shandong Agr Univ, Coll Food Sci & Engn, Tai An 271018, Peoples R China
[3] Shandong Prov Inst Control Agrochem, Jinan 250131, Peoples R China
基金
中国国家自然科学基金;
关键词
Competitive ELISA; Weak competitive molecule; Estrogen receptor; Estrogen disrupting chemicals; Molecular docking; IN-VITRO; AFFINITY; MILK;
D O I
10.1016/j.foodchem.2022.134084
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Enzyme labeled competitive molecules are generally homologous with competitors in competitive broad-spectrum enzyme-linked immunosorbent assays (ELISA). It is speculated that the detectability will be improved when the competitiveness of competitive molecule is weak. Herein, common small molecule food hazard-estrogen disrupting chemicals (EDCs) were used as target model for verification. The dual-estrogen receptor (ER) and three estrogen-enzyme conjugates with various responses were used as recognizers and competitive molecules in ELISA. ELISA based on bisphenol (BPA)-horseradish peroxidase (HRP) has the highest detectability and can screen all six EDCs, in which BPA-HRP showed the weakest ER excitatory activity (Ka = 1.39 x 10(-2) nmol center dot L-1) among three conjugates. The proposal showed good practicability with spiked recovery of 80.0-110 % for estrogens (17 beta-estradiol, 17 alpha-estradiol, BPA) in foodstuffs, and revealed biomarkers with weak competitiveness may be applied to other competitive procedures to improve detectability, and it provides sen-sitive pre-screening strategy for follow-up screening tool.
引用
收藏
页数:8
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