In silico maturation of affinity and selectivity of DNA aptamers against aflatoxin B1 for biosensor development

被引:39
作者
Mousivand, Maryam [1 ,2 ]
Anfossi, Laura [3 ,4 ,7 ]
Bagherzadeh, Kowsar [5 ,6 ]
Barbero, Nadia [3 ,4 ,7 ]
Mirzadi-Gohari, Amir [1 ]
Javan-Nikkhah, Mohammad [1 ]
机构
[1] Univ Tehran, Coll Agr Sci & Engn, Dept Plant Protect, Karaj 3158777871, Iran
[2] Agr Res Educ & Extens Org, Agr Biotechnol Res Inst Iran, Microbial Biotechnol Dept, Karaj 3135933151, Iran
[3] Univ Turin, Dept Chem, Via Pietro Giuria 5,7, I-10125 Turin, Italy
[4] Univ Turin, NIS Interdept Ctr, Via Pietro Giuria 5,7, I-10125 Turin, Italy
[5] Iran Univ Med Sci, Rassoul Akram Hosp, Eye Res Ctr, Five Senses Inst, Tehran, Iran
[6] Iran Univ Med Sci, Razi Drug Res Ctr, Tehran, Iran
[7] Univ Turin, Dept Chem, Via Giuria 5, I-10125 Turin, Italy
关键词
Aflatoxin B-1; Aptamer; Molecular docking; Fluorescent anisotropy; Genetic algorithm; Gold nanoparticles; APTASENSOR; VITRO;
D O I
10.1016/j.aca.2020.01.045
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A high affinity and selectivity DNA aptamer for aflatoxin B-1 (AFB(1)) was designed through Genetic Algorithm (GA) based in silico maturation (ISM) strategy. The sequence of a known AFB(1) aptamer (Patent: PCT/CA2010/001292, Apt1) applied as a probe in many aptasensors was modified using seven GA rounds to generate an initial library and three different generations of ss DNA oligonucleotides as new candidate aptamers. Molecular docking methodology was used to screen and analyze the best aptamere-AFB(1) complexes. Also, a new pipeline was proposed to faithfully predict the tertiary structure of all single stranded DNA sequences. By the second generation, aptamer Apt1 sequence was optimized in the local search space and five aptamers including F20, g12, C52, C32 and H1 were identified as the best aptamers for AFB(1). The selected aptamers were applied as probes in an unmodified gold nanoparticles-based aptasensor to evaluate their binding affinity to AFB(1) and their selectivity against other mycotoxins (aflatoxins B-2, G(1), G(2), M-1, ochratoxin A and zearalenone). In addition, a novel direct fluorescent anisotropy aptamer assay was developed to confirm the binding interaction of the selected aptamers over AFB(1). The ISM allowed the identification of an aptamer, F20, with up to 9.4 and 2 fold improvement in affinity and selectivity compared to the parent aptamer, respectively. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:178 / 186
页数:9
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