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Simple label-free fluorescence detection of apurinic/apyrimidinic endonuclease 1 activity and its inhibitor using the abasic site-binding fluorophore

机译:简单的无标记荧光检测嘌呤/嘧啶核糖核酸内切酶1活性及其抑制剂,使用无碱基位点结合荧光团

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Apurinic/apyrimidinic endonuclease 1 (APE1) plays crucial role in DNA repair, which cleaves the abasic site (AP site) to facilitate the DNA repair process. APE1 is overexpressed in several cancers, and it has been demonstrated to be a promising target for anticancer drugs. Thus, development of a method for the detection of APE1 activity and screening of its inhibitors is important and highly desirable for cancer diagnosis and therapy. In this study, we report a simple and label-free fluorescence detection method for APE1 activity using an AP site-binding dye (2-amino-5,6,7-trimethyl-1,8-naphthyridine, ATMND) as a signal indicator. The fluorescence of ATMND was quenched after inserting ATMND into the AP site with a C base at the opposite position. The APE1-catalyzed cleavage of the AP site resulted in the release of the bound ATMND, and the quenched fluorescence of ATMND recovered. The label-free strategy makes this method convenient and easy to manipulate. The proposed method exhibits a good sensitivity, and we have also employed it to evaluate the inhibition effect of a drug on the APE1 activity. This approach holds potential applications in APE1-related cancer diagnosis and anticancer drug screening.
机译:apurinic / apyrimidinic内切核酸酶1(APE1)在DNA修复中起着至关重要的作用,该酶切割无碱基位点(AP位点)以促进DNA修复过程。 APE1在几种癌症中过表达,并且已被证明是抗癌药物的有希望的靶标。因此,开发用于检测APE1活性并筛选其抑制剂的方法是重要的,并且对于癌症的诊断和治疗是非常需要的。在这项研究中,我们报告了一种简单且无标签的APE1活性荧光检测方法,该方法使用AP位点结合染料(2-氨基-5,6,7-三甲基-1,8-萘啶,ATMND)作为信号指示剂。将ATMND插入具有相反位置C碱基的AP位点后,ATMND的荧光被淬灭。 AP位点的APE1催化裂解导致结合的ATMND释放,并且ATMND的猝灭荧光得以恢复。无标签策略使此方法方便且易于操作。所提出的方法显示出良好的敏感性,并且我们还使用它来评估药物对APE1活性的抑制作用。这种方法在APE1相关的癌症诊断和抗癌药物筛选中具有潜在的应用。

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