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Structural study of DNA duplexes containing the (6–4) photoproduct by fluorescence resonance energy transfer

机译:通过荧光共振能量转移对包含(6–4)光产物的DNA双链体进行结构研究

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摘要

Fluorescence resonance energy transfer (FRET) experiments have been performed to elucidate the structural features of oligonucleotide duplexes containing the pyrimidine(6–4)pyrimidone photoproduct, which is one of the major DNA lesions formed at dipyrimidine sites by UV light. Synthetic 32mer duplexes with and without the (6–4) photoproduct were prepared and fluorescein and tetramethylrhodamine were attached, as a donor and an acceptor, respectively, to the aminohexyl linker at the C5 position of thymine in each strand. Steady-state and time-resolved analyses revealed that both the FRET efficiency and the fluorescence lifetime of the duplex containing the (6–4) photoproduct were almost identical to those of the undamaged duplex, while marked differences were observed for a cisplatin-modified duplex, as a model of kinked DNA. Lifetime measurements of a series of duplexes containing the (6–4) photoproduct, in which the fluorescein position was changed systematically, revealed a small unwinding at the damage site, but did not suggest a kinked structure. These results indicate that formation of the (6–4) photoproduct induces only a small change in the DNA structure, in contrast to the large kink at the (6–4) photoproduct site reported in an NMR study.
机译:已经进行了荧光共振能量转移(FRET)实验,以阐明含有嘧啶(6–4)嘧啶酮光产物的寡核苷酸双链体的结构特征,这是双嘧啶位点在紫外光下形成的主要DNA损伤之一。制备具有和不具有(6–4)光产物的合成32mer双链体,并将荧光素和四甲基罗丹明分别作为供体和受体连接到每条链中胸腺嘧啶C5位置的氨基己基接头上。稳态和时间分辨分析表明,包含(6–4)光产物的双链体的FRET效率和荧光寿命几乎与未损伤的双链体相同,而顺铂修饰的双链体则观察到显着差异,作为纽结DNA的模型。一系列包含(6–4)光产物的双链体的终生测量表明,荧光素的位置发生了系统性的改变,显示出在损伤部位有少量的展开,但并未显示出扭结的结构。这些结果表明(6–4)光产物的形成仅引起DNA结构的微小变化,这与NMR研究中报道的(6–4)光产物位点的大扭结相反。

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