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Direct Revelation of Multiple Conformations in RNA by Femtosecond Dynamics

机译:飞秒动力学直接揭示RN​​A中的多个构象

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摘要

The intrinsic dynamics of RNA structures occur on a wide range of length and time scales, implying structural flexibility or heterogeneity. The role of conformational dynamics in molecular recognition and functions, however, is not well understood. Despite significant advances in traditional and new spectroscopic methodologies, it is still difficult to extract information on both the exact nature of the heterogeneous conformations and their quantitative distributions. Here we demonstrate a femtosecond dynamics approach for probing the multiple conformations coexisting in RNAs. We focus primarily on mapping the base stacking patterns. The observed base stacking/ unstacking rates in the single strand are typically in the range of 100—500 ns. This means that, for a time window much shorter than the nanosecond regime, the distributions of stacking patterns are static and can potentially be analyzed by ultrafast spectroscopy.
机译:RNA结构的内在动力学发生在各种长度和时间尺度上,这暗示了结构的灵活性或异质性。但是,尚未很好地理解构象动力学在分子识别和功能中的作用。尽管传统和新的光谱学方法取得了重大进展,但仍然难以提取有关异构构象的确切性质及其定量分布的信息。在这里,我们演示了一种飞秒动力学方法,用于探测RNA中共存的多种构象。我们主要专注于映射基本堆栈模式。单链中观察到的碱基堆积/堆积速度通常在100-500 ns的范围内。这意味着,对于比纳秒制短得多的时间窗口,堆叠模式的分布是静态的,并且有可能通过超快光谱法进行分析。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2007年第14期|p.4118-4119|共2页
  • 作者

    Liang Zhao; Tianbing Xia;

  • 作者单位

    Department of Molecular and Cell Biology, The University of Texas at Dallas, Richardson, Texas 75083-0688;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

  • 入库时间 2022-08-18 03:21:12

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