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中国生物工程杂志

CHINA BIOTECHNOLOGY
中国生物工程杂志  2016, Vol. 36 Issue (7): 21-26    DOI: 10.13523/j.cb.20160704
研究报告     
基于CDR2和CDR3区随机突变筛选抗黄曲霉毒素B1单域重链抗体的研究
庞倩1, 马榆1, 李诚1, 刘韫滔1, 刘书亮1, 王小红2, 刘爱平
1 四川农业大学食品学院 雅安 625014;
2 华中农业大学食品科学技术学院 武汉 430070
Screening of Anti-aflatoxin B1 Single Domain Heavy Chain Antibody Based on Random Mutation of CDR2 and CDR3 Regions
PANG Qian1, MA Yu1, LI Cheng1, LIU Yun-tao1, LIU Shu-liang1, WANG Xiao-hong2, LIU Ai-ping
1 College of Food Science, Sichuan Agricultural University, Yaan 625014, China;
2 College of Food Science and technology, Huazhong Agricultural University, Wuhan 430070, China
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摘要:

基于抗原-抗体特异性反应的免疫学方法是黄曲霉毒素B1的常用检测方法。为制备针对AFB1的抗体,综合参考已报道的噬菌体文库筛选的抗AFB1单域重链抗体(variable domain of heavy chain of heavy chain antibody,VHH)序列,合成一条经密码子优化[适于大肠杆菌(Escherichia coli,E. coli)表达]的高同源性序列。在抗AFB1 VHH的CDR2和CDR3区引入部分随机突变,构建噬菌体抗体库。采用phage-ELISA技术,以AFB1O-OVA为包被抗原,淘选单域重链抗体库,经过4轮筛选,获得15株能与AFB1特异性结合的阳性克隆。以结合力最高的1株克隆为材料,扩增相应的VHH基因,构建表达质粒pET-22b-VHH。在E. coli BL21(DE3)中表达VHH,经间接竞争ELISA分析,获得的抗AFB1 VHH的灵敏度约为10μg/mL。

关键词: Phage-ELISA单域重链抗体随机突变黄曲霉毒素B1    
Abstract:

Immunoassay, based on antigen-antibody reaction, was one of the common methods employed to detect AFB1. In order to prepare antibody against AFB1, A codon-optimized DNA sequence (suitable for expression in Escherichia coli (E. coli)) of high homology was synthesized according to comprehensive screening of a large number of anti-AFB1 VHH sequences obtained through phage display library. A phage antibody library was constructed by introducing random mutations in part of CDR2 and CDR3 regions of the synthesized anti-AFB1 VHH. Anti-AFB1 VHH of high affinity was screened through phage-ELISA, using AFB1-OVA as coating antigen. After four rounds of screening, 15 clones capable of binding to AFB1 were obtained. VHH gene of the clone with highest binding ability was amplified, and applied to construct expression plasmid pET-22b-VHH. The corresponding VHH protein was expressed in E. coli BL21(DE3). According to indirect competitive ELISA, the sensitivity of anti-AFB1 VHH obtained was about 10μg/ml.

Key words: VHH    Phage-ELISA    AFB1    Random mutation
收稿日期: 2016-01-29 出版日期: 2016-07-25
ZTFLH:  Q511  
通讯作者: 刘爱平     E-mail: aipliu@outlook.com
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引用本文:

庞倩, 马榆, 李诚, 刘韫滔, 刘书亮, 王小红, 刘爱平. 基于CDR2和CDR3区随机突变筛选抗黄曲霉毒素B1单域重链抗体的研究[J]. 中国生物工程杂志, 2016, 36(7): 21-26.

PANG Qian, MA Yu, LI Cheng, LIU Yun-tao, LIU Shu-liang, WANG Xiao-hong, LIU Ai-ping. Screening of Anti-aflatoxin B1 Single Domain Heavy Chain Antibody Based on Random Mutation of CDR2 and CDR3 Regions. China Biotechnology, 2016, 36(7): 21-26.

链接本文:

https://manu60.magtech.com.cn/biotech/CN/10.13523/j.cb.20160704        https://manu60.magtech.com.cn/biotech/CN/Y2016/V36/I7/21

[1] 郭婷,张宇昊,马良.纳米抗体的特性及其应用研究进展.食品科学,2013,34(3):294-297.Guo T,Zhang Y H,Ma L.Properties and application prospects of nano-antibody in food industry.Food Science,2013,34(3):294-297.
[2] 冯敬敬.盐酸克伦特罗ELISA检测方法的建立及其纳米抗体的筛选.天津:天津大学,化工学院,2012,173.Feng G G.Establishment of ELISA for Clenbuterol and Screening of Nanoantibody.Tianjian:Tianjian University,School of Chemical Engineering and Technology,2012,173.
[3] 吴石金,孙培龙.简明免疫学原理.北京:化学工业出版社,2008:11-12.Wu J S,Sun J L.Concise Immunology Principle.Beijing:Chemical Industry Press,2008:11-12.
[4] 冯仁青,郭振泉.现代抗体技术及其应用.北京:北京大学出版社,2006:55-76.Feng R Q,Guo Z Q.Modern Antibody Technique and Its Application.Beijing:Beijing University Press,2006:55-76.
[5] Marla D,Swain a,George P,et al.Immunodiagnostic reagents using llama single domain antibody-alkaline phosphatase fusion proteins.Analytical Biochemistry,2011,417(2):188-194.
[6] 朱莉莉,李建东,梁米芳.基因工程抗体分泌影响因素研究进展.中国医药生物技术,2008,3(3):229-231.Zhu L L,Li J D,Liang M F.Advances in factors that affect engineered antibody secretion.Chin Med Biotechnol,2008,3(3):229-231.
[7] 姜忍忍,许超,周小理,等.纳米抗体的应用及其研究新进展.生命的化学,2013,33(3):307-315.Jiang R R,Xu C,Zhou X L,et al.Application and the research progress of nanobodies.Chemistry of Life,2013,33(3):307-315.
[8] Yau K Y F,Lee H,Hall J C,et al.Emerging trends in the synthesis and improvement of hapten-specific recombinant antibodies.Biothechnology Advances,2003,21(7):599-637.
[9] 秦海艳,毛晓燕,乔玉玲,等.单链抗体的研究进展.现代生物医学进展,2011,11(4):795-797.Qin H Y,Mao X Y,Qiao Y L,et al.Progress in single-chain antibody.Progress in Modern Biomedicine,2011,11(4):795-797.
[10] 朱磊,张大鹏.天然小分子抗体研究进展.药学学报,2012,47(10):1281-1286.Zhu L,Zhang D P.Advances in the study of natural small molecular antibody.Acta Pharmaceutica Sinica,2012,47(10):1281-1286.
[11] 刘微,张敏,郭春燕,等.骆驼纳米抗体在医疗领域研究进展.动物医学进展,2013,34(3):101-105.Liu W,Zhang M,Guo C Y,et al.Progress on camel nanobodies in medical field.Progress in Veterinary Medicine,2013,34(3):101-105.
[12] 杨珂,王冬.纳米抗体及其应用.细胞与分子免疫学杂志,2008,24(4):425-427.Yang K,Wang D.Introduction and application of nano-antibody.Chinese Journal of Cellular and Molecular Immunology,2008,24(4):425-427.
[13] 蔡家麟,夏立亮,潘欣,等.重链抗体的结构特点及其应用前景分析.生命科学,2013,25(9):853-857.Cai J L,Xia L L,Pan X,et al.Structure properties of heavy chain antibody and its future application.Chinese Bulletin of Life Sciences,2013,25(9):853-857.
[14] International Agency for Research Cancer (IARC).Aflatoxins.In:Some Naturally Occurring Substances:Food Items and Constituents,Heterocyclic Aromatic Amines and Mycotoxins.Lyon,France:IARC,1993:245-395.
[15] 韩春卉,江涛,李燕俊,等.黄曲霉毒素B1酶联免疫试剂盒稳定性研究.食品科学,2013,34(14):315-318.Han C H,Jiang T,Li Y J,et al.Stability of Aflatoxin B1 ELISA kit.Food Science,2013,34(14):315-318.
[16] 郑海燕,魏帅,郭波莉,等.挤压膨化降解糙米中黄曲霉毒素B1.食品科学,2014,35(14):35-39.Zheng H Y,Wei S,Guo B L,et al.Reduction of Aflatoxin B1 in brown rice by extrusion cooking.Food Science,2014,35(14):35-39.
[17] 涂追.基于单域重链抗体的天然噬菌体文库的构建及抗DON适配体的淘选.江西:南昌大学,食品学院,2010.Tu Z.Construction of Natural Phage Display Library of VHH and Screening of Aptamer Against DON.Jiangxi:Nanchang University,School of Food Science&Technology,2010.
[18] Osborne J,Jermutus L,Duncan A.Current methods for the generation of human antibodies for the treatment of autoimmune diseases.Drug Discov Today,2003,8(18):845.
[19] 阎岩,白文涛,徐志凯,等.重链可变区基因随机CDR3 ScFv噬菌体抗体库的构建及筛选.细胞与分子免疫学杂志,2000,16(2):171-173.Yan Y,Bai W T,Xu Z K,et al.Construction and screening of ScFv phage repertoire with random CDR3 of VH gene.Chinese Journal of Cellular and Molecular Immunology,2000,16(2):171-173.
[20] Hoogenboom H R,de Bruine A P,Hufton S E,et al.Antibody phage display technology and its applications.Immunotechnology,1998,4(1):1-20.
[21] 涂追,许杨,刘夏,等.驼源天然单域重链抗体库的构建与鉴定.中国生物工程杂志,2011,31(4):31-36.Tu Z,Xu Y,Liu X,et al.Construction and biopanning of camelid Naǐve Single-domain antibody phage display library.China Biotechnology,2011,31(4):31-36.
[22] Lloyd C,Lowe D,Edwards B,et al.Modelling the human immune response:performance of a 1011 human antibody repertoire against a broad panel of therapeutically relevant antigens.Protein Engineering Design and Selection,2009,22(3):159-168.
[23] He T,Wang Y,Li P,et al.Nanobody-based enzyme immunoassay for aflatoxin in agro-products with high tolerance to cosolvent methanol.Analytical chemistry,2014,86(17):8873-8880.

[1] 庞倩,陈晶,王小红,王佳. 基于噬菌体展示技术抗黄曲霉毒素B1单链抗体的筛选及其蛋白结构分析 *[J]. 中国生物工程杂志, 2018, 38(12): 41-48.
[2] 涂追, 许杨, 刘夏, 何庆华, 陶勇. 驼源天然单域重链抗体库的构建与鉴定[J]. 中国生物工程杂志, 2011, 31(04): 31-36.
[3] 刘大岭,沈奕,*,姚冬生. 一种新的检测黄曲霉毒素B1的酶生物传感器的制作[J]. 中国生物工程杂志, 2008, 28(3): 44-52.
[4] 耿旭, 李骏, 左翼, 吴自荣. 亚硝酸钠体外随机突变枯草杆菌纤溶酶基因及其产物性质研究[J]. 中国生物工程杂志, 2005, 25(6): 61-64.
[5] 贾向东, 陈德富, 陈喜文, 郭少影. 几种定向进化技术的比较及文库构建策略[J]. 中国生物工程杂志, 2003, 23(12): 68-72.
[6] 吴小平, 阎锡蕴. 噬菌体抗体库技术制备高亲和力人抗体[J]. 中国生物工程杂志, 2002, 22(3): 29-32.