Establishment of a sensitive time-resolved fluoroimmunoassay for detection of Bacillus thuringiensis Cry1Ie toxin based nanobody from a phage display library
文献类型: 外文期刊
作者: Xu, Chongxin 1 ; Liu, Xiaoqin; Zhang, Cunzheng 1 ; Zhang, Xiao 1 ; Zhong, Jianfeng 1 ; Liu, Yuan 1 ; Hu, Xiaodan 1 ; L 1 ;
作者机构: 1.Jiangsu Acad Agr Sci, Inst Food Qual Safety & Detect, Key Lab Food Qual & Safety Jiangsu, Prov State Key Lab Breeding Base, Nanjing 210014, Jiangsu, Peoples R China
2.Jiangsu Acad Agr Sci, Inst F
关键词: Cry1Ie toxin;Phage display library;Nanobody;Time-resolved fluoroimmunoassay (TRFIA)
期刊名称:ANALYTICAL BIOCHEMISTRY ( 影响因子:3.365; 五年影响因子:3.049 )
ISSN: 0003-2697
年卷期: 2017 年 518 卷
页码:
收录情况: SCI
摘要: Cry1Ie toxin was an insect-resistant protein used in genetically modified crops (GMC). In this study, a large human VH gene nanobodies phage displayed library was employed to select anti-Cry1Ie toxin antibody by affinity panning. After 5 rounds of panning, total 12 positive monoclonal phage particles were obtained. One of the identified positive phage nanobody was expressed in E.coli BL21 and the purified protein was indicated as a molecular mass of approximately 20 kDa by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). Then a sensitive indirect competitive time-resolved fluoroimmunoassay (IC-TRFIA) was established for detection of Cry1Ie toxin by the purified protein. The working range of detection for Cry1Ie toxin standards in the IC-TRFIA were 0.08-6.44 ng mL(-1) and the medium inhibition of control (IC50) was 0.73 ng mL(-1). It showed a weak cross-reactivity with Cry1Ab toxin (at 5.6%), but did not recognize Cry1B, Cry1C, Cry1F, and Cry2A toxins (were <0.1%). The average recoveries of Cry1Ie toxin from respectively spiked in rice, corn and soil samples were in the range of 83.5%-96.6% and with a coefficient of variation (CV) among 2.0%-8.6%. These results showed the IC-TRFIA was promising for detection of Cry1Ie toxin in agricultural and environmental samples. (C) 2016 Elsevier Inc. All rights reserved.
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