Construction of an immunized rabbit phage display antibody library for screening microcystin-LR high sensitive single-chain antibody

被引:25
|
作者
Xu, Chongxin [1 ,2 ]
Miao, Wenjie [1 ]
He, Yan [3 ]
Zu, Yao [1 ]
Liu, Xiaoqin [4 ]
Li, Jianhong [1 ]
Liu, Xianjin [2 ]
机构
[1] Nanjing Normal Univ, Coll Life Sci, Nanjing 210023, Jiangsu, Peoples R China
[2] Jiangsu Acad Agr Sci, Inst Food Safety & Nutr, Minist Sci & Technol, Lab Food Qual,Safety State Key Lab Cultivat Base, Nanjing 210014, Jiangsu, Peoples R China
[3] Chinese Acad Agr Sci, Inst Food Sci & Technol, Beijing 100081, Peoples R China
[4] Huaihua Vocat & Tech Coll, Huaihua 418007, Peoples R China
基金
中国国家自然科学基金;
关键词
Microcystin; Polyclonal antibodies; Phage display antibody library; ScFv; Immunoassay; TIME-RESOLVED FLUOROIMMUNOASSAY; RECOMBINANT PROTEIN EXPRESSION; VARIABLE FRAGMENT SCFV; SELECTION-STRATEGIES; AFFINITY MATURATION; ESCHERICHIA-COLI; NANOBODY LIBRARY; IMMUNOASSAY; TOXIN; TOXICITY;
D O I
10.1016/j.ijbiomac.2018.11.122
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Microcystin-LR (MC-LR) is one of the most common biotoxin that pollutes water and agricultural products. The study aims to obtain the high sensitive anti-MC-LR single-chain antibody (scFv) for detecting MC-LR. Here, a MC-LR-immunized rabbit phage display scFv library with its capacity of 3.26 x 10(9) CFU/mL was constructed and used for anti-MC-LR phage scFv particles screening. After four rounds of biopanning, 18 positives were isolated and identified successfully. The most positive scFv (RscFv3) was expressed in Escherichia coli HB2151 and purified with a concentration of 796.7 mu g/mL, and the purified anti-MC-LR polyclonal antibodies (PAbs) were 3.6 mg/mL. The PAbs and scFv based indirect competitive enzyme linked immunosorbent assay (IC-ELISAs) were established for MC-LR and its analogues, and the results showed they all had high sensitive for MC-LR with detection limits of 0.03 and 0.05 mu g/L, and had strong cross-reactivity for MC-RR, MC-WR and MC-YR, respectively. The average recovery rate was 91.9% with coefficient of variation <6.8% for scFv-based IC-ELISA to detect MC-LR spiked in water samples, which met the requirement of indoor testing. The present results indicate that we have obtained a high sensitive anti-MC-LR scFv by the MC-LR-immunized phage library construction and screening, and the scFv-based IC-ELISA can be used for monitoring MC-LR in water samples. (C) 2018 Published by Elsevier B.V.
引用
收藏
页码:369 / 378
页数:10
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