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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Aequorin as a sensitive and selective reporter for detection of dopamine: A photoprotein inhibition assay approach
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Aequorin as a sensitive and selective reporter for detection of dopamine: A photoprotein inhibition assay approach

机译:Aequorin作为一种敏感和选择性的报告,用于检测多巴胺:光蛋白抑制测定方法

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摘要

Dopamine is a metabolite that plays a key role in the human body and in biomedical and diagnostic applications. Thus, the concentration of this analyte has been considered in various diseases in therapeutic drug monitoring (TDM). In the present study, for the first time, a photoprotein inhibition assay strategy was developed by utilizing aequorin for the direct detection of dopamine as a receptor and reporter simultaneously. The results showed that bioluminescence emission of aequorin was effectively quenched by increasing concentration of dopamine at the range of 1 nM to 100 mu M with a detection limit of 53 nM. The viability of this method for the monitoring of dopamine in spiked biological fluids was also established and it was successfully applied for the direct determination of dopamine in a blood serum and urine without preliminary treatment with satisfactory quantitative recovery 90-95% and 82-93%, respectively. The structural investigation using circular dichroism, fluorescence spectroscopy, and docking simulation indicated that, changes in the microenvironment of aromatic residues were significant, while minor conformational alterations of the protein were observed. It seems dopamine inhibits bioluminescence activity with specific binding to the residues involved in the light production. (C) 2018 Elsevier B.V. All rights reserved.
机译:多巴胺是一种代谢物,在人体和生物医学和诊断应用中起着关键作用。因此,在治疗药物监测(TDM)的各种疾病中,已经考虑了该分析物的浓度。在本研究中,首次通过利用Aequorin同时直接检测多巴胺作为受体和报告者来开发光蛋白抑制测定策略。结果表明,通过增加1nm至100μm的多巴胺浓度,有效地淬灭Aequorin的生物发光排放,检测限为53nm。还建立了这种方法对掺掺态生物流体中多巴胺进行监测的可行性,成功地应用于血清和尿液中多巴胺的直接测定,而无需初步处理,令人满意的定量回收率90-95%和82-93% , 分别。使用圆形二色性,荧光光谱学和对接模拟的结构研究表明,芳族残基的微环境的变化显着,而观察到蛋白质的次要构象改变。似乎多巴胺抑制了与涉及光产生的残留物的特异性结合的生物发光活性。 (c)2018年elestvier b.v.保留所有权利。

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