A sensitive and selective fluorescent probe for acetylcholinesterase: Synthesis, performance, mechanism and application

The detection of acetylcholinesterase (AChE) activity is of great significance for studying the physiological functions of AChE and clinical diagnosis of pesticide poisoning. Herein, a small-molecule fluorescent probe BDFA was rationally designed and readily synthesized via a one-step reaction, whic...

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Main Authors: Meng Yao, Hailiang Nie, Wenxue Yao, Xueping Yang, Guowei Zhang
Format: Article
Language:English
Published: Elsevier 2022-07-01
Series:Arabian Journal of Chemistry
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1878535222002453
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author Meng Yao
Hailiang Nie
Wenxue Yao
Xueping Yang
Guowei Zhang
author_facet Meng Yao
Hailiang Nie
Wenxue Yao
Xueping Yang
Guowei Zhang
author_sort Meng Yao
collection DOAJ
description The detection of acetylcholinesterase (AChE) activity is of great significance for studying the physiological functions of AChE and clinical diagnosis of pesticide poisoning. Herein, a small-molecule fluorescent probe BDFA was rationally designed and readily synthesized via a one-step reaction, which enables qualitative and quantitative detection of AChE. BDFA emits a slight fluorescence in an aqueous medium, while the fluorescence is significantly enhanced under the catalysis of AChE. Mechanism studies reveal that BDFA eliminates the N, N-dimethyl carbamate protective group in the presence of AChE and then spontaneously undergoes intramolecular cyclization conversion to generate an intense fluorescent product. Based on the above mechanism, BDFA exhibits a sensitive, selective, rapid and stable “turn-on” fluorescence response to AChE, without interference from pH, ions, thiols, amino acids and other enzymes. The fluorescence intensity of BDFA at 525 nm has a linear relationship with the AChE concentration in the range of 0.0045–1.0 U/mL, and the detection limit is 4.5 mU/mL. Moreover, BDFA is suitable for rapidly diagnosing AChE activity in blood samples, thus providing an efficient and convenient tool for diagnosing organophosphorus and carbamate pesticide poisoning. Compared with the reported AChE fluorescent probes, BDFA exhibits apparent advantages including simple synthesis, low detection limit and fast response speed.
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spelling doaj.art-fc1f652df98e46e181c2714fb81b79752022-12-22T03:23:09ZengElsevierArabian Journal of Chemistry1878-53522022-07-01157103929A sensitive and selective fluorescent probe for acetylcholinesterase: Synthesis, performance, mechanism and applicationMeng Yao0Hailiang Nie1Wenxue Yao2Xueping Yang3Guowei Zhang4Key Laboratory of Public Health Safety of Hebei Province, College of Public Health, Hebei University, Baoding 071002, Hebei, ChinaKey Laboratory of Public Health Safety of Hebei Province, College of Public Health, Hebei University, Baoding 071002, Hebei, China; Corresponding authors.Key Laboratory of Public Health Safety of Hebei Province, College of Public Health, Hebei University, Baoding 071002, Hebei, ChinaKey Laboratory of Public Health Safety of Hebei Province, College of Public Health, Hebei University, Baoding 071002, Hebei, ChinaHebei Collaborative Innovation Center of Tumor Microecological Metabolism Regulation, College of Traditional Chinese Medicine, Hebei University, Baoding 071002, Hebei, China; Corresponding authors.The detection of acetylcholinesterase (AChE) activity is of great significance for studying the physiological functions of AChE and clinical diagnosis of pesticide poisoning. Herein, a small-molecule fluorescent probe BDFA was rationally designed and readily synthesized via a one-step reaction, which enables qualitative and quantitative detection of AChE. BDFA emits a slight fluorescence in an aqueous medium, while the fluorescence is significantly enhanced under the catalysis of AChE. Mechanism studies reveal that BDFA eliminates the N, N-dimethyl carbamate protective group in the presence of AChE and then spontaneously undergoes intramolecular cyclization conversion to generate an intense fluorescent product. Based on the above mechanism, BDFA exhibits a sensitive, selective, rapid and stable “turn-on” fluorescence response to AChE, without interference from pH, ions, thiols, amino acids and other enzymes. The fluorescence intensity of BDFA at 525 nm has a linear relationship with the AChE concentration in the range of 0.0045–1.0 U/mL, and the detection limit is 4.5 mU/mL. Moreover, BDFA is suitable for rapidly diagnosing AChE activity in blood samples, thus providing an efficient and convenient tool for diagnosing organophosphorus and carbamate pesticide poisoning. Compared with the reported AChE fluorescent probes, BDFA exhibits apparent advantages including simple synthesis, low detection limit and fast response speed.http://www.sciencedirect.com/science/article/pii/S1878535222002453AcetylcholinesteraseFluorescent probeRapid detectionPesticide poisoning
spellingShingle Meng Yao
Hailiang Nie
Wenxue Yao
Xueping Yang
Guowei Zhang
A sensitive and selective fluorescent probe for acetylcholinesterase: Synthesis, performance, mechanism and application
Arabian Journal of Chemistry
Acetylcholinesterase
Fluorescent probe
Rapid detection
Pesticide poisoning
title A sensitive and selective fluorescent probe for acetylcholinesterase: Synthesis, performance, mechanism and application
title_full A sensitive and selective fluorescent probe for acetylcholinesterase: Synthesis, performance, mechanism and application
title_fullStr A sensitive and selective fluorescent probe for acetylcholinesterase: Synthesis, performance, mechanism and application
title_full_unstemmed A sensitive and selective fluorescent probe for acetylcholinesterase: Synthesis, performance, mechanism and application
title_short A sensitive and selective fluorescent probe for acetylcholinesterase: Synthesis, performance, mechanism and application
title_sort sensitive and selective fluorescent probe for acetylcholinesterase synthesis performance mechanism and application
topic Acetylcholinesterase
Fluorescent probe
Rapid detection
Pesticide poisoning
url http://www.sciencedirect.com/science/article/pii/S1878535222002453
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