Khaksarinejad Reza, Mohsenifar Afshin, Rahmani-Cherati Tavoos, Karami Rezvan, Tabatabaei Meisam
Department of Toxicology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
Appl Biochem Biotechnol. 2015 May;176(2):359-71. doi: 10.1007/s12010-015-1579-1. Epub 2015 Apr 1.
Rapid detection of organophosphorous (OP) compounds such as paraoxon would allow taking immediate decision on efficient decontamination procedures and could prevent further damage and potential casualties. In the present study, a biosensor based on nanomagnet-silica core-shell conjugated to organophosphorous hydrolase (OPH) enzyme was designed for detection of paraoxon. Coumarin1, a competitive inhibitor of the OPH enzyme, was used as a fluorescence-generating molecule. Upon excitation of cumarin1 located at the active site of the enzyme, i.e., OPH, the emitted radiations were intensified due to the mirroring effect of the nanomagnet-silica core-shell conjugated to the enzyme. In presence of paraoxon and consequent competition with the fluorophore in occupying enzyme's active site, a significant reduction in emitted radiations was observed. This reduction was proportional to paraoxon concentration in the sample. The method worked in the 10- to 250-nM concentration range had a low standard deviation (with a coefficient of variation (CV) of 6-10%), and the detection limit was as low as 5 × 10(-6) μM.
快速检测对氧磷等有机磷(OP)化合物,有助于就有效的去污程序立即做出决策,并可防止进一步损害和潜在伤亡。在本研究中,设计了一种基于与有机磷水解酶(OPH)共轭的纳米磁体-二氧化硅核壳结构的生物传感器,用于检测对氧磷。香豆素1,一种OPH酶的竞争性抑制剂,被用作产生荧光的分子。当位于酶(即OPH)活性位点的香豆素1受到激发时,由于与酶共轭的纳米磁体-二氧化硅核壳结构的镜像效应,发射的辐射会增强。在存在对氧磷并因此与荧光团竞争占据酶活性位点的情况下,观察到发射辐射显著减少。这种减少与样品中对氧磷的浓度成正比。该方法在10至250 nM的浓度范围内有效,标准偏差较低(变异系数(CV)为6-10%),检测限低至5×10(-6) μM。