A thiamine-triggered fluormetric assay for acetylcholinesterase activity and inhibitor screening based on oxidase-like activity of MnO2 nanosheets

Acetylcholinesterase (AChE) plays an essential role in biological signal transmission, the aberrant expression of which could cause diverse neurodegenerative diseases. Herein, based on the oxidase-like activity of manganese dioxide nanosheets (MnO2 NSs), we found that MnO2 NSs could directly oxidize thiamine into intensely fluorescent thiochrome without the need of peroxides. When AChE was introduced, acetylthiocholine could be hydrolyzed to generate thiocholine, which efficiently triggered the reduction of MnO2 NSs into Mn2+, resulting in the decrease of fluorescence. Owing to the inhibiting effect of tacrine to the AChE activity, the decomposition of MnO2 was hindered, thus leading to the fluorescence recovery. According to the above mechanism, we constructed a simple, low-cost, label-free, facile and rapid synthetic fluorescent biosensor for highly sensitive and selective detection of AChE activity and screening of its inhibitor. This biosensor obtained a good linear range from 0.02 to 1 mU/mL and an extremely low detection limit of 15 U/mL for AChE assay, as well as a sensitive screening for tacrine and an excellent applicability in human serum samples. These results suggested that our proposed method would be potentially applied in monitoring the disease progression.

Automated summary

Acetylcholinesterase (AChE) activity can be detected using manganese dioxide nanosheets (MnO2 NSs) to oxidize thiamine into fluorescent thiochrome. This low-cost biosensor offers highly sensitive detection of AChE activity and screening of inhibitors, showing great potential for monitoring disease progression.