Caratelli Veronica, Fillo Silvia, D'Amore Nino, Rossetto Ornella, Pirazzini Marco, Moccia Maria, Avitabile Concetta, Moscone Danila, Lista Florigio, Arduini Fabiana
Tor Vergata University, Department of Chemical Science and Technologies, Via Della Ricerca Scientifica, 00133, Rome, Italy.
Scientific Department, Army Medical Center, Via Santo Stefano Rotondo, 4-00184, Rome, Italy.
Biosens Bioelectron. 2021 Jul 1;183:113210. doi: 10.1016/j.bios.2021.113210. Epub 2021 Apr 1.
Botulinum neurotoxins (BoNTs) produced by soil bacterium Clostridium botulinum are cause of botulism and listed as biohazard agents, thus rapid screening assays are needed for taking the correct countermeasures in a timely fashion. The gold standard method relies on the mouse lethality assay with a lengthy analysis time, i.e., 2-5 days, hindering the prompt management of food safety and medical diagnosis. Herein, we propose the first paper-based antibody-free sensor for reliable and rapid detection of BoNT/A and BoNT/C, exploiting their cleavage capability toward a synthetic peptide able to mimic the natural substrate SNAP-25. The peptide is labelled with the electroactive molecule methylene blue and immobilized on the paper-based electrode modified with gold nanoparticles. Because BoNT/A and BoNT/C can cleave the peptide with the removal of methylene blue from electrode surface, the presence of these neurotoxins in the sample leads to a signal decrease proportional to BoNT amount. The biosensor developed with the selected peptide and combined with smartphone assisted potentiostat is able to detect both BoNT/A and BoNT/C with a linearity up to 1 nM and a detection limit equal to 10 pM. The applicability of this biosensor was evaluated with spiked samples of orange juice, obtaining recovery values equal to 104 ± 6% and 98 ± 9% for 1 nM and 0.5 nM of BoNT/A, respectively.
由土壤细菌肉毒杆菌产生的肉毒杆菌神经毒素(BoNTs)是肉毒中毒的病因,被列为生物危害剂,因此需要快速筛选检测方法以便及时采取正确的应对措施。金标准方法依赖于小鼠致死性试验,分析时间较长,即2至5天,这阻碍了食品安全和医学诊断的及时管理。在此,我们提出了第一种基于纸的无抗体传感器,用于可靠、快速地检测BoNT/A和BoNT/C,利用它们对能够模拟天然底物SNAP-25的合成肽的切割能力。该肽用具有电活性的分子亚甲蓝标记,并固定在修饰有金纳米颗粒的纸基电极上。由于BoNT/A和BoNT/C可以切割该肽,使亚甲蓝从电极表面去除,样品中这些神经毒素的存在会导致信号下降,下降幅度与BoNT的量成正比。用所选肽开发并与智能手机辅助恒电位仪相结合的生物传感器能够检测BoNT/A和BoNT/C,线性范围高达1 nM,检测限等于10 pM。用橙汁加标样品评估了该生物传感器的适用性,对于1 nM和0.5 nM的BoNT/A,回收率分别为104±6%和98±9%。