Department of Chemistry, Dinabandhu Mahavidyalaya, Bongaon, West Bengal 743235, India; CSIR-Indian Institute of Chemical Biology, Kolkata 700 032, India.
Government GD College, Keshiary, Paschim Medinipur, West Bengal 721135, India.
J Photochem Photobiol B. 2020 Mar;204:111804. doi: 10.1016/j.jphotobiol.2020.111804. Epub 2020 Jan 25.
The ubiquitous influence of double stranded RNAs in biological events makes them imperative to gather data based on specific binding procedure of small molecules to various RNA conformations. Particular interest may be attributed to situations wherein small molecules target RNAs altering their structures and causing functional modifications. The main focus of this study is to delve into the interactive pattern of two small molecule phenothiazinium dyes, methylene blue and new methylene blue, with three duplex RNA polynucleotides-poly(A).poly(U), poly(C).poly(G) and poly(I).poly(C) by spectroscopic and molecular modeling techniques. Analysis of data as per Scatchard and Benesi-Hildebrand methodologies revealed highest affinity of these dyes to poly(A).poly(U) and least to poly(I).poly(C). In addition to fluorescence quenching, viscometric studies also substantiated that the dyes follow different modes of binding to different RNA polynucleotides. Distortion in the RNA structures with induced optical activity in the otherwise optically inactive dye molecules was evidenced from circular dichroism results. Dye-induced RNA structural modification occurred from extended conformation to compact particles visualized by atomic force microscopy. Molecular docking results revealed different binding patterns of the dye molecules within the RNA duplexes. The novelty of the present work lies towards a new contribution of the phenothiazinium dyes in dysfunctioning double stranded RNAs, advancing our knowledge to their potential use as RNA targeted small molecules.
双链 RNA 在生物事件中的普遍影响使得基于小分子与各种 RNA 构象的特定结合程序来收集数据变得至关重要。特别感兴趣的可能是小分子靶向 RNA 改变其结构并引起功能修饰的情况。本研究的主要重点是深入研究两种小分子吩噻嗪染料亚甲蓝和新亚甲蓝与三种双链 RNA 多核苷酸-多(A).多(U)、多(C).多(G)和多(I).多(C)之间的相互作用模式通过光谱和分子建模技术。根据 Scatchard 和 Benesi-Hildebrand 方法分析数据表明,这些染料对多(A).多(U)的亲和力最高,对多(I).多(C)的亲和力最低。除了荧光猝灭外,粘度研究还证实染料以不同的模式与不同的 RNA 多核苷酸结合。圆二色性结果表明,诱导无光学活性的染料分子产生光学各向异性,表明 RNA 结构发生了扭曲。原子力显微镜观察到,染料诱导的 RNA 结构修饰从扩展构象到紧凑颗粒。分子对接结果揭示了染料分子在 RNA 双链体中的不同结合模式。本工作的新颖之处在于吩噻嗪染料在功能失调的双链 RNA 中的新贡献,这增加了我们对其作为 RNA 靶向小分子潜在用途的认识。