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Sensitive detection of acid phosphatase enzyme and screening of inhibitors using an anionic poiyfluorene derivative

机译:使用阴离子聚芴衍生物灵敏检测酸性磷酸酶并筛选抑制剂

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摘要

An assay method, that includes a ferric iron bound to a novel anionic water soluble polymer (P1), is developed, for the continuous and real time fluorescent amplification detection of acid phosphatase' (ACP) enzyme activity under acidic conditions in nanomolar quantities. The ferric iron bound P1 offers a sensitive and rapid turn on assay for inorganic phosphate (Pi) selectively. The most frequently used phosphatase substrate p-nitro phenyl phosphate (p-NPP), which was inactive towards the dequenching of P1-Fe~(3+) fluorescence, has been utilized in the study as a model compound for the enzymatic hydrolysis and a very small concentration of enzyme in nanomolar regime was sufficient to generate a significant fluorometric change during enzymatic hydrolysis. Kinetic parameters were derived by observing the fluorometric changes of P1 during enzymatic hydrolysis providing vital information on the changes observed in the enzyme kinetics in a competitive environment. Additionally, this assay also offers high throughput screening of ACP inhibitors that may render the usefulness of this method in drug discovery.
机译:开发了一种测定方法,该方法包括与新型阴离子水溶性聚合物(P1)结合的三价铁,用于在纳摩尔量的酸性条件下连续和实时荧光扩增检测酸性磷酸酶(ACP)的酶活性。三价铁结合的P1选择性地提供了灵敏且快速的无机磷酸盐(Pi)检测方法。对P1-Fe〜(3+)荧光的去猝灭没有活性的最常用的磷酸酶底物对硝基苯基磷酸酯(p-NPP)已在研究中用作模型化合物进行酶促水解和纳摩尔浓度下非常低的酶浓度足以在酶促水解过程中产生显着的荧光变化。动力学参数是通过观察酶解过程中P1的荧光变化得出的,从而提供了有关竞争环境中酶动力学变化的重要信息。另外,该测定法还提供了高通量的ACP抑制剂筛选,这可能使该方法在药物发现中有用。

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