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Silver Nanoclusters-Based Fluorescence Assay of Protein Kinase Activity and Inhibition

机译:基于银纳米簇的蛋白激酶活性和抑制荧光测定

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摘要

A simple and sensitive fluorescence method for monitoring the activity and inhibition of protein kinase (PKA) has been developed using polycytosine oligonucleotide (dC12)-templated silver nanoclusters (Ag NCs). Adenosine-5'-triphosphate (ATP) was found to enhance the fluorescence of Ag NCs, while the hydrolysis of ATP to adenosine diphosphate (ADP) by PKA decreased the fluorescence of Ag NCs. Compared to the existing methods for kinase activity assay, the developed method does not involve phosphorylation of the substrate peptides, which significantly simplifies the detection procedures. The method exhibits high sensitivity, good selectivity, and wide linear range toward PKA detection. The inhibition effect of kinase inhibitor H-89 on the activity of PKA was also studied. The sensing protocol was also applied to the assay of drug-stimulated activation of PKA in HeLa cell lysates.
机译:使用聚胞嘧啶寡核苷酸 (dC12) 模板的银纳米团簇 (Ag NCs) 开发了一种简单灵敏的荧光方法来监测蛋白激酶 (PKA) 的活性和抑制作用。发现腺苷-5'-三磷酸(ATP)增强了Ag NCs的荧光,而PKA将ATP水解为二磷酸腺苷(ADP)降低了Ag NCs的荧光。 与现有的激酶活性测定方法相比,所开发的方法不涉及底物肽的磷酸化,大大简化了检测程序。该方法灵敏度高,选择性好,对PKA检测线性范围宽。还研究了激酶抑制剂H-89对PKA活性的抑制作用。该传感方案还应用于HeLa细胞裂解物中药物刺激的PKA激活的测定。

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