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基于酯酶-2突变体的纳米结构安培生物传感器用于对氧磷(神经毒素)的选择性测定。

Esterase-2 mutant-based nanostructured amperometric biosensors for the selective determination of paraoxon (Neurotoxin).

作者信息

Magar Hend Samy, Fayez Muhammad, Febbraio Ferdinando, Hassan Rabeay Y A

机构信息

Applied Organic Chemistry Department, National Research Centre (NRC), Dokki, Giza, 2622, Egypt.

Biosensors Research Lab, Zewail City of Science and Technology, 6th October City, Giza, 12578, Egypt.

出版信息

Anal Biochem. 2025 Mar;698:115751. doi: 10.1016/j.ab.2024.115751. Epub 2024 Dec 15.

Abstract

Organophosphate pesticides (OPs) are causing non-selective inhibition in enzymatic bioreceptors, thus the enzymatic-inhibition-based traditional assays are not suitable for their specific detection in food and environmental samples. Accordingly, a selective nanostructured electrochemical biosensing system was designed using six mutants of the esterase-2 (EST2 protein) enzymes from A. acidocaldarius to be exploited as targeting bio-receptors for the specific detection of OPs. Each of the EST2 mutant enzymes was immobilized on disposable screen-printed electrodes modified with Aluminum oxide (AlO)/Copper (Cu) nanocomposite. Consequently, chronoamperometric assay was fully optimized, and cross-reactivity study was carried out using paraoxon, malathion and chlorpyrifos. The comparative cross-reactivity study was performed on the six mutant proteins in terms of inhibitory percentage over a wide range of pesticide concentrations. Eventually, a wide dynamic inhibition range was achieved while the limit of detection for the paraoxon toxicity was 0.01 nM and the limit of quantification was 0.05 nM. Finally, paraoxon was selectively determined using the newly developed EST-based biosensor in different spiked food samples.

摘要

有机磷酸酯类农药(OPs)会对酶促生物受体产生非选择性抑制作用,因此基于酶抑制的传统检测方法并不适用于在食品和环境样品中对其进行特异性检测。相应地,利用嗜酸热硫化叶菌(A. acidocaldarius)酯酶-2(EST2蛋白)的六个突变体设计了一种选择性纳米结构电化学生物传感系统,将其用作特异性检测OPs的靶向生物受体。每个EST2突变酶都固定在经氧化铝(AlO)/铜(Cu)纳米复合材料修饰的一次性丝网印刷电极上。随后,对计时电流分析法进行了全面优化,并使用对氧磷、马拉硫磷和毒死蜱进行了交叉反应性研究。在广泛的农药浓度范围内,对六种突变蛋白进行了抑制百分比方面的比较交叉反应性研究。最终,实现了较宽的动态抑制范围,对氧磷毒性的检测限为0.01 nM,定量限为0.05 nM。最后,使用新开发的基于EST的生物传感器对不同加标食品样品中的对氧磷进行了选择性测定。

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