Hewitt Sarah H, Ali Rozee, Mailhot Romain, Antonen Chloe R, Dodson Charlotte A, Butler Stephen J
Department of Chemistry , Loughborough University , Epinal Way , Loughborough , LE11 3TU , UK . Email:
Department of Pharmacy & Pharmacology , University of Bath , Claverton Down , Bath , BA2 7AY , UK.
Chem Sci. 2019 May 1;10(20):5373-5381. doi: 10.1039/c9sc01552c. eCollection 2019 May 28.
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.
消耗和产生核苷多磷酸(NPP)阴离子的酶是药物研发中的主要靶点。例如,蛋白激酶是抗癌药物靶点中最大的类别之一。准确测定酶动力学和作用机制是药物研发研究的关键环节。为了增强对先导药物化合物选择的信心,制药研究人员拥有可靠且经济实惠的检测方法来准确测量酶活性至关重要。我们提出了一种简单、灵敏的微孔板检测方法,用于实时监测一系列产生NPP阴离子的具有药学重要性的酶反应,包括激酶和糖基转移酶。我们的检测方法利用一种单一、稳定的铕(III)配合物,它与NPP阴离子可逆结合,通过时间分辨发光来指示酶反应过程中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检测方法的重大局限性,无需昂贵的抗体或设备、化学标记的底物或产物以及分离或纯化步骤。我们的无标记和无抗体方法能够对酶活性和抑制作用进行快速定量分析,为药物研发提供了一种潜在的强大工具,适用于抑制剂的高通量筛选以及酶动力学参数的准确测量。