Aleksandra Bednarz, Rebecca Torp Rosendal, Line Mørkholt Lund, Victoria Birkedal
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引用次数: 0
摘要
G-quadruplexes (G4s) 是一种螺旋状四链核酸结构,可在富含鸟嘌呤的序列中形成,主要存在于端粒、启动子和 DNA 复制源等细胞功能区。目前,人们正努力以这些结构为靶点,开发用于新型抗癌、神经和病毒疗法的特异性小分子 G4 结合剂。在这里,我们介绍了一种基于淬灭 DNA G-四联体固有荧光的光学检测方法,用于评估和比较各种小分子配体在溶液中的 G4 结合亲和力。我们的研究表明,这种方法可以直接量化配体与不同 G4 拓扑的结合。我们相信,这种方法将有助于快速、可靠地评估小分子 G4 配体,并支持它们的开发。
Probing G-quadruplex-ligand binding using DNA intrinsic fluorescence.
G-quadruplexes (G4s) are helical four-stranded nucleic acid structures that can form in guanine-rich sequences, which are mostly found in functional cellular regions, such as telomeres, promoters, and DNA replication origins. Great efforts are being made to target these structures towards the development of specific small molecule G4 binders for novel anti-cancer, neurological, and viral therapies. Here, we introduce an optical assay based on quenching of the intrinsic fluorescence of DNA G-quadruplexes for assessing and comparing the G4 binding affinity of various small molecule ligands in solutions. We show that the approach allows direct quantification of ligand binding to distinctive G4 topologies. We believe that this method will facilitate quick and reliable evaluation of small molecule G4 ligands and support their development.