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ADP-Glo:一种用于激酶的生物发光均相ADP监测检测方法。

ADP-Glo: A Bioluminescent and homogeneous ADP monitoring assay for kinases.

作者信息

Zegzouti Hicham, Zdanovskaia Marina, Hsiao Kevin, Goueli Said A

机构信息

Promega Corporation, Madison, Wisconsin 53711, USA.

出版信息

Assay Drug Dev Technol. 2009 Dec;7(6):560-72. doi: 10.1089/adt.2009.0222.

Abstract

ADP-Glo is a novel bioluminescent, homogeneous assay for monitoring ADP producing biochemical reactions and thus it is an ideal assay for detecting enzyme activity using a wide variety of substrates. It is a universal assay that can be used with protein kinases, lipid kinases, sugar kinases, and many more kinases as well as ATPases. Because of its high sensitivity, it is suitable for monitoring enzyme activities at very early substrate conversions requiring very low amount of enzymes. Furthermore, as the assay is applicable to a broad range of ATP and substrate concentrations, it is optimal for enzymes that require high ATP and substrate concentrations. This is critical since inhibitor potency has to be demonstrated at the cellular level where ATP is present at millimolar concentrations. ADP-Glo is performed in 2 steps upon completion of kinase reaction: a combined termination of kinase reaction and depletion of remaining ATP in the first step, and conversion of generated ADP to ATP and the newly produced ATP to light output using luciferase/luciferin reaction in the second step. The luminescent signal generated is proportional to the ADP concentration produced and is correlated with the kinase activity. Due to its high signal to background and luminescent readout, this assay is less susceptible to generation of false hits and thus it is applicable to not only primary and secondary screening but also kinase profiling.

摘要

ADP-Glo是一种新型的生物发光均相分析方法,用于监测产生ADP的生化反应,因此是使用多种底物检测酶活性的理想分析方法。它是一种通用分析方法,可用于蛋白激酶、脂质激酶、糖激酶以及更多激酶和ATP酶。由于其高灵敏度,它适用于在底物转化率非常低、需要极少量酶的早期阶段监测酶活性。此外,由于该分析方法适用于广泛的ATP和底物浓度范围,对于需要高ATP和底物浓度的酶来说是最佳选择。这一点至关重要,因为必须在细胞水平(其中ATP浓度为毫摩尔级)证明抑制剂的效力。在激酶反应完成后,ADP-Glo分两步进行:第一步是激酶反应的联合终止和剩余ATP的消耗,第二步是使用荧光素酶/荧光素反应将生成的ADP转化为ATP,并将新产生的ATP转化为光输出。产生的发光信号与产生的ADP浓度成正比,并与激酶活性相关。由于其高信噪比和发光读数,该分析方法不易产生假阳性结果,因此不仅适用于一级和二级筛选,也适用于激酶谱分析。

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