Amplified fluorescent aptasensor through catalytic recycling for highly sensitive detection of ochratoxin A

• Published in: Biosensors & bioelectronics 2015-03, Vol.65, p.16-22
• Main Authors: Wei, Yin, Zhang, Ji, Wang, Xu, Duan, Yixiang
• Format: Article
• Language: English
• Subjects: Amplification; Amplified detection; Aptamers, Nucleotide - chemistry; Assaying; Biomolecules; Biosensing Techniques - methods; Catalysis; Deoxyribonuclease I - chemistry; DNA aptamer; Dyes; Fluoresceins - chemistry; Fluorescence; Fluorescent Dyes - chemistry; Graphite - chemistry; Limit of Detection; Mycotoxins - analysis; Nano-graphite; Nanostructure; Nanostructures - chemistry; Ochratoxin A; Ochratoxins - analysis; Recycling; Spectrometry, Fluorescence - methods; Vitaceae; Wine - analysis; Wines
• ISSN: 0956-5663; 1873-4235
• DOI: 10.1016/j.bios.2014.09.100

This paper describes a novel approach utilizing nano-graphite–aptamer hybrid and DNase I for the amplified detection of ochratoxin A (OTA) for the first time. Nano-graphite can effectively quench the fluorescence of carboxyfluorescein (FAM) labeled OTA specific aptamer due to their strong π–π; stacking interactions; while upon OTA addition, it will bind with aptamer to fold into an OTA–aptamerG-quadruplex structure, which does not adsorb on the surface of nano-graphite and thus retains the dye fluorescence. Meanwhile, the G-quadruplex structure can be cleaved by DNase I, and in such case OTA is delivered from the complex. The released OTA then binds other FAM-labeled aptamers on the nano-graphite surface, and touches off another target recycling, resulting in the successive release of dye-labeled aptamers from the nano-graphite, which leads to significant amplification of the signal. Under the optimized conditions, the present amplified sensing system exhibits high sensitivity toward OTA with a limit of detection of 20nM (practical measurement), which is about 100-fold higher than that of traditional unamplified homogeneous assay. Our developed method also showed high selectivity against other interference molecules and can be applied for the detection of OTA in real red wine samples. The proposed assay is simple, cost-effective, and might open a door for the development of new assays for other biomolecules. This aptasensor is of great practical importance in food safety and could be widely extended to the detection of other toxins by replacing the sequence of the recognition aptamer. •Using nano-graphite–aptamer and DNase I for highly sensitive detection of OTA for the first time.•The sensitivity of proposed assay is 100-fold higher than homogeneous assay.•The cost of using nano-graphite is much lower than homogeneous assay using traditional nanomaterials.•The proposed assay can be expanded to detect other biomolecules.