首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Direct visualization of the quadruplex structures in human chromosome using FRET: Application of quadruplex stabilizer and duplex-binding fluorophore
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Direct visualization of the quadruplex structures in human chromosome using FRET: Application of quadruplex stabilizer and duplex-binding fluorophore

机译:使用FRET直接可视化人类染色体中的四链体结构:四链体稳定剂和双链体结合荧光团的应用

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摘要

The G-quadruplex structures in the telomere of a chromosome can not only protect the internal chromosome sequences by preventing the improper activation of DNA-damage-response pathways but also become targets for cancer treatments. In this manuscript, we wish to prove the existence of G-quadruplex structure formation, rather than G-quadruplex sequence, in chromosome of human cancer cells. Based on our studies, the fluorescent mapping of G-quadruplex structures in the chromosome is possible with the combination of G-quadruplex targeting fluorophore (BMVC, 3, 6-bis-(1-methyl-4-vinylpyridinium)-carbazole diiodide) and duplex-binding fluorophores (Hoechst or propidium iodide). By means of an applicable incubation time between cell cycle period and proper staining procedure to the chromosome, FRET (fluorescence resonance energy transfer) between G-quadruplex targeting fluorophore and duplex-binding fluorophore can increase the signal contrast of the fluorescent color and the fluorescent mapping of quadruplex structures can be easily observed using fluorescence microscopy. These observations are further supported by basic spectral analysis, titration binding assay, gel electrophoresis binding competition assay and confocal microscopy.
机译:染色体端粒中的G-四链体结构不仅可以通过防止DNA损伤反应途径的不当激活来保护内部染色体序列,还可以成为癌症治疗的目标。在本文中,我们希望证明在人类癌细胞的染色体中存在G-四链体结构形成,而不是G-四链体序列。根据我们的研究,结合G-四链体靶向荧光团(BMVC,3,6-双-(1-甲基-4-乙烯基吡啶)-咔唑二碘化物)和G-四链体靶向荧光体,可以对染色体上的G-四链体结构进行荧光定位。双重结合的荧光团(赫斯特或碘化丙啶)。通过在细胞周期和适当的染色体染色程序之间适当的孵育时间,G-四链体靶向荧光团和双链结合荧光团之间的FRET(荧光共振能量转移)可以增加荧光色和荧光图谱的信号对比度使用荧光显微镜可以很容易地观察到四链体结构。这些观察结果进一步得到基本光谱分析,滴定结合测定,凝胶电泳结合竞争测定和共聚焦显微镜的支持。

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