Minoshima Masafumi, Matsumoto Tetsuaki, Kikuchi Kazuya
Graduate School of Engineering, ‡Institute for Academic Initiatives, and §Immunology Frontier Research Center, Osaka University , Suita, Osaka 565-0871, Japan.
Anal Chem. 2014 Aug 5;86(15):7925-30. doi: 10.1021/ac501881s. Epub 2014 Jul 8.
We designed a simple, rapid, and continuous method for the detection of the activity of histone deacetylases (HDACs), which are key enzymes involved in epigenetic gene regulation, using a DNA-based fluorogenic probe. We designed and synthesized a fluorogenic probe, BOXTO-GK(Ac)G, which is a DNA staining dye-peptide conjugate containing an acetylated lysine. The DNA-dependent fluorescence of BOXTO-GK(Ac)G was greatly enhanced upon deacetylation of the acetylated lysine moiety, owing to the increased DNA binding ability of the probe. The HDAC reaction was detected through a simple procedure that combined this probe with DNA. Our detection system monitored the enzymatic reaction in real time and could be applied to the inhibition assay. These findings demonstrated that our system might be a useful tool for the analysis of HDAC function and for the evaluation of the inhibitor potencies of drug candidates that target HDACs.
我们设计了一种简单、快速且连续的方法,用于检测组蛋白去乙酰化酶(HDACs)的活性。HDACs是参与表观遗传基因调控的关键酶,该方法使用基于DNA的荧光探针。我们设计并合成了一种荧光探针BOXTO-GK(Ac)G,它是一种含有乙酰化赖氨酸的DNA染色染料-肽缀合物。由于探针与DNA结合能力的增强,乙酰化赖氨酸部分去乙酰化后,BOXTO-GK(Ac)G的DNA依赖性荧光大大增强。通过将该探针与DNA相结合的简单程序来检测HDAC反应。我们的检测系统可实时监测酶促反应,并可应用于抑制测定。这些发现表明,我们的系统可能是分析HDAC功能以及评估靶向HDAC的候选药物抑制剂效力的有用工具。