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首页> 外文期刊>Chemical science >A simple, robust, universal assay for real-time enzyme monitoring by signalling changes in nucleoside phosphate anion concentration using a europium(iii)-based anion receptor
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A simple, robust, universal assay for real-time enzyme monitoring by signalling changes in nucleoside phosphate anion concentration using a europium(iii)-based anion receptor

机译:使用基于((iii)的阴离子受体,通过发出信号改变核苷磷酸根阴离子浓度的变化,进行实时酶监测的简单,强大,通用的分析方法

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Enzymes that consume and produce nucleoside polyphosphate (NPP) anions represent major targets in drug discovery. For example, protein kinases are one of the largest classes of drug targets in the fight against cancer. The accurate determination of enzyme kinetics and mechanisms is a critical aspect of drug discovery research. To increase confidence in the selection of lead drug compounds it is crucial that pharmaceutical researchers have robust, affordable assays to measure enzyme activity accurately. We present a simple, sensitive microplate assay for real-time monitoring of a range of pharmaceutically important enzyme reactions that generate NPP anions, including kinases and glycosyltransferases. Our assay utilises a single, stable europium( III ) complex that binds reversibly to NPP anions, signalling the dynamic changes in NPP product/substrate ratio during an enzyme reaction using time-resolved luminescence. This supramolecular approach to enzyme monitoring overcomes significant limitations in existing assays, obviating the need for expensive antibodies or equipment, chemically labelled substrates or products and isolation or purification steps. Our label and antibody-free method enables rapid and quantitative analysis of enzyme activities and inhibition, offering a potentially powerful tool for use in drug discovery, suitable for high-throughput screening of inhibitors and accurate measurements of enzyme kinetic parameters.
机译:消耗并产生核苷多磷酸根(NPP)阴离子的酶是药物发现中的主要目标。例如,蛋白激酶是对抗癌症中最大的药物靶标之一。酶动力学和机理的准确测定是药物发现研究的关键方面。为了增加对先导化合物的选择的信心,至关重要的是,药物研究人员必须具有可靠的,负担得起的测定方法,以准确地测量酶活性。我们提出了一种简单,灵敏的微孔板检测法,用于实时监测产生NPP阴离子(包括激酶和糖基转移酶)的一系列重要的药物重要酶反应。我们的测定利用单个稳定的euro(III)络合物,该络合物可逆地与NPP阴离子结合,从而在使用时间分辨发光的酶反应过程中,指示NPP产物/底物比率的动态变化。这种用于酶监测的超分子方法克服了现有测定法的重大局限,从而消除了对昂贵的抗体或设备,化学标记的底物或产物以及分离或纯化步骤的需求。我们的无标记和无抗体方法能够快速,定量地分析酶的活性和抑制作用,为发现药物提供了潜在强大的工具,适用于抑制剂的高通量筛选和酶动力学参数的准确测量。

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