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

适体 化学 生物信息学 寡核苷酸 DNA 选择性 黄曲霉毒素 生物化学 计算生物学 组合化学 色谱法 分子生物学 基因 生物 食品科学 催化作用
作者
Maryam Mousivand,Laura Anfossi,Kowsar Bagherzadeh,Nadia Barbero,Amir Mirzadi-Gohari,M. Javan‐Nikkhah
出处
期刊:Analytica Chimica Acta [Elsevier BV]
卷期号:1105: 178-186 被引量:38
标识
DOI:10.1016/j.aca.2020.01.045
摘要

A high affinity and selectivity DNA aptamer for aflatoxin B1 (AFB1) was designed through Genetic Algorithm (GA) based in silico maturation (ISM) strategy. The sequence of a known AFB1 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 aptamer-AFB1 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 AFB1. The selected aptamers were applied as probes in an unmodified gold nanoparticles-based aptasensor to evaluate their binding affinity to AFB1 and their selectivity against other mycotoxins (aflatoxins B2, G1, G2, M1, 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 AFB1. 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.

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