首页> 美国卫生研究院文献>Nucleic Acids Research >Verification of specific G-quadruplex structure by using a novel cyanine dye supramolecular assembly: II. The binding characterization with specific intramolecular G-quadruplex and the recognizing mechanism
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Verification of specific G-quadruplex structure by using a novel cyanine dye supramolecular assembly: II. The binding characterization with specific intramolecular G-quadruplex and the recognizing mechanism

机译:通过使用新型花菁染料超分子组装验证特定的G-四链体结构:II.。特定分子内G-四链体的结合表征及识别机理

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摘要

The supramolecular assembly of a novel cyanine dye, 3,3′-di(3-sulfopropyl)-4,5,4′,5′-dibenzo-9-ethyl-thiacarbocyanine triethylammonium salt (ETC) was designed to verify specific intramolecular G-quadruplexes from duplex and single-strand DNAs. Spectral results have shown that ETC presented two major distinct signatures with specific intramolecular G-quadruplexes in vitro: (i) dramatic changes in the absorption spectra (including disappearance of absorption peak around 660 nm and appearance of independent new peak around 584 nm); (ii) ∼70 times enhancement of fluorescence signal at 600 nm. Furthermore, based on 1H-nuclear magnetic resonance and circular dichroism results, the preferring binding of ETC to specific intramolecular G-quadruplexes probably result from end-stacking, and the loop structure nearby also plays an important role.
机译:设计新型花菁染料3,3'-二(3-磺丙基)-4,5,4',5'-二苯并-9-乙基-硫代羰基花青三乙铵盐(ETC)的超分子组装以验证特定的分子内G -来自双链和单链DNA的四链体。光谱结果表明,ETC在体外具有特定分子内G四联体的两个主要特征:(i)吸收光谱的剧烈变化(包括660 nm附近吸收峰的消失和584 nm附近独立的新峰的出现); (ii)在600 nm处荧光信号增强约70倍。此外,基于 1 H核磁共振和圆二色性结果,ETC与特定分子内G四联体的优先结合可能是由于末端堆积,附近的环结构也起重要作用。

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