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Exploring the preferential interaction of quercetin with VEGF promoter G-quadruplex DNA and construction of a pH-dependent DNA-based logic gate

机译:探索槲皮素与VEGF启动子G-四链体DNA的优先相互作用以及基于pH的DNA逻辑门的构建

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G-Quadruplex DNA (G4–DNA) is one of the most important non-canonical nucleic acid structures. G4–DNA forming sequences are present in different crucial genomic regions and are abundant in promoter regions of several oncogenes. Therefore, G4–DNA is an important target for anticancer drugs and hence binding interactions between G4–DNA and small molecule ligands are of great importance. Since G4–DNA is a highly polymorphic structure, it is important to identify ligand molecules which preferentially target a particular quadruplex sequence in comparison to other quadruplexes. In the present study, different spectroscopic techniques have been used to explore the interaction of the dietary plant flavonoid quercetin (Que) with various G4–DNA structures (VEGF, c-MYC, c-KIT1, c-KIT2, h-TELO) along with double stranded (duplex) DNA. We found that Que shows preferential interaction with VEGF G4–DNA compared to other G4–DNA structures as well as duplex DNA. This identifies Que as an appropriate natural product based ligand for targeting VEGF G4–DNA. We also observed pH dependent interaction of Que with VEGF G4–DNA, based on which we have designed a complex Boolean logic gate exploiting Que as a sensing molecule.
机译:G-四链体DNA(G4-DNA)是最重要的非规范核酸结构之一。 G4–DNA形成序列存在于不同的关键基因组区域,并且在几个癌基因的启动子区域中丰富。因此,G4-DNA是抗癌药物的重要靶标,因此G4-DNA与小分子配体之间的结合相互作用非常重要。由于G4-DNA是高度多态的结构,因此与其他四链体相比,鉴定优先靶向特定四链体序列的配体分子非常重要。在本研究中,不同的光谱技术已被用于探索日粮植物类黄酮槲皮素(Que)与各种G4-DNA结构(VEGF,c-MYC,c-KIT1,c-KIT2,h-TELO)的相互作用。具有双链(双链)DNA。我们发现Que与VEGF G4-DNA相比,与其他G4-DNA结构以及双链体DNA优先相互作用。这表明Que是靶向VEGF G4-DNA的合适的基于天然产物的配体。我们还观察到Que与VEGF G4-DNA的pH依赖性相互作用,在此基础上,我们设计了一个复杂的布尔逻辑门,利用Que作为传感分子。

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