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Folding dynamics and conformational heterogeneity of human telomeric G-quadruplex structures in Na+ solutions by single molecule FRET microscopy

机译:单分子FRET显微镜观察Na +溶液中人端粒G-四链体结构的折叠动力学和构象异质性

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摘要

G-quadruplex structures can occur throughout the genome, including at telomeres. They are involved in cellular regulation and are potential drug targets. Human telomeric G-quadruplex structures can fold into a number of different conformations and show large conformational diversity. To elucidate the different G-quadruplex conformations and their dynamics, we investigated telomeric G-quadruplex folding using single molecule FRET microscopy in conditions where it was previously believed to yield low structural heterogeneity. We observed four FRET states in Na+ buffers: an unfolded state and three G-quadruplex related states that can interconvert between each other. Several of these states were almost equally populated at low to medium salt concentrations. These observations appear surprising as previous studies reported primarily one G-quadruplex conformation in Na+ buffers. Our results permit, through the analysis of the dynamics of the different observed states, the identification of a more stable G-quadruplex conformation and two transient G-quadruplex states. Importantly these results offer a unique view into G-quadruplex topological heterogeneity and conformational dynamics.
机译:G-四链体结构可以出现在整个基因组中,包括端粒。它们参与细胞调节并且是潜在的药物靶标。人端粒G-四链体结构可以折叠成许多不同的构象,并显示出很大的构象多样性。为了阐明不同的G-四链体构象及其动力学,我们在以前认为其产生低结构异质性的条件下,使用单分子FRET显微镜研究了端粒G-四链体折叠。我们在Na + 缓冲区中观察到四个FRET状态:一个展开状态和三个可以相互转换的G四元相关的状态。在中低盐浓度下,其中几个州的人口几乎相等。这些观察结果令人惊讶,因为先前的研究主要报道了Na + 缓冲液中的一种G-四链体构象。我们的结果通过分析不同观察状态的动力学,可以鉴定出更稳定的G-四链体构象和两个瞬时G-四链体态。重要的是,这些结果为G-四链体拓扑异质性和构象动力学提供了独特的视角。

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