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Dietary Compound Resveratrol Is a Pan-BET Bromodomain Inhibitor

机译:膳食化合物白藜芦醇是Pan-BET溴结构域抑制剂

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摘要

The chemopreventive and anticancer effects of resveratrol (RSV) are widely reported in the literature. Specifically, mechanisms involving epigenetic regulation are promising targets to regulate tumor development. Bromodomains act as epigenetic readers by recognizing lysine acetylation on histone tails and boosting gene expression in order to regulate tissue-specific transcription. In this work, we showed that RSV is a pan-BET inhibitor. Using Differential Scanning Fluorimetry (DSF), we showed that RSV at 100 µM increased the melting temperature (∆Tm) of BET bromodomains by around 2.0 °C. The micromolar dissociation constant (Kd) range was characterized using Isothermal Titration Calorimetry (ITC). The RSV Kd value accounted to 6.6 µM in case of BRD4(1). Molecular docking proposed the binding mode of RSV against BRD4(1) mimicking the acetyl-lysine interactions. All these results suggest that RSV can also recognize epigenetic readers domains by interacting with BET bromodomains.
机译:白藜芦醇(RSV)的化学预防和抗癌作用已在文献中广泛报道。具体而言,涉及表观遗传调控的机制是调控肿瘤发展的有希望的靶标。 Bromodomains通过识别组蛋白尾巴上的赖氨酸乙酰化并增强基因表达来调控组织特异性转录,从而成为表观遗传学阅读器。在这项工作中,我们证明了RSV是pan-BET抑制剂。使用差示扫描荧光法(DSF),我们发现100 µM的RSV使BET溴结构域的熔融温度(∆Tm)提高了约2.0°C。使用等温滴定量热法(ITC)表征微摩尔解离常数(Kd)范围。对于BRD4(1),RSV Kd值为6.6 µM。分子对接提出了RSV对BRD4(1)的模仿乙酰-赖氨酸相互作用的结合模式。所有这些结果表明,RSV还可以通过与BET溴结构域相互作用来识别表观遗传阅读器结构域。

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