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使用时间分辨荧光和多元分析方法研究 i -motif DNA 的构象转变。

Study of conformational transitions of i-motif DNA using time-resolved fluorescence and multivariate analysis methods.

机构信息

Department of Chemical Engineering and Analytical Chemistry, University of Barcelona, Martí i Franquès 1-11, E-08028 Barcelona, Spain.

Univ. Lille, CNRS, UMR 8516 - LASIR - Laboratoire de Spectrochimie Infrarouge et Raman, F-59000 Lille, France.

出版信息

Nucleic Acids Res. 2019 Jul 26;47(13):6590-6605. doi: 10.1093/nar/gkz522.

Abstract

Recently, the presence of i-motif structures at C-rich sequences in human cells and their regulatory functions have been demonstrated. Despite numerous steady-state studies on i-motif at neutral and slightly acidic pH, the number and nature of conformation of this biological structure are still controversial. In this work, the fluorescence lifetime of labelled molecular beacon i-motif-forming DNA sequences at different pH values is studied. The influence of the nature of bases at the lateral loops and the presence of a Watson-Crick-stabilized hairpin are studied by means of time-correlated single-photon counting technique. This allows characterizing the existence of several conformers for which the fluorophore has lifetimes ranging from picosecond to nanosecond. The information on the existence of different i-motif structures at different pH values has been obtained by the combination of classical global decay fitting of fluorescence traces, which provides lifetimes associated with the events defined by the decay of each sequence and multivariate analysis, such as principal component analysis or multivariate curve resolution based on alternating least squares. Multivariate analysis, which is seldom used for this kind of data, was crucial to explore similarities and differences of behaviour amongst the different DNA sequences and to model the presence and identity of the conformations involved in the pH range of interest. The results point that, for i-motif, the intrachain contact formation and its dissociation show lifetimes ten times faster than for the open form of DNA sequences. They also highlight that the presence of more than one i-motif species for certain DNA sequences according to the length of the sequence and the composition of the bases in the lateral loop.

摘要

最近,已经证明了在富含 C 的人类细胞序列中存在 i-motif 结构及其调节功能。尽管在中性和略酸性 pH 值下对 i-motif 进行了大量的稳态研究,但这种生物结构的构象的数量和性质仍然存在争议。在这项工作中,研究了不同 pH 值下标记分子信标 i-motif 形成 DNA 序列的荧光寿命。通过时间相关单光子计数技术研究了侧环中碱基的性质和沃森-克里克稳定发夹的存在对其的影响。这允许对几种构象进行特征化,其中荧光团的寿命范围从皮秒到纳秒。通过对荧光轨迹的经典全局衰减拟合进行组合,获得了不同 pH 值下存在不同 i-motif 结构的信息,该拟合提供了与每个序列的衰减相关的寿命以及多元分析,例如主成分分析或基于交替最小二乘法的多元曲线分辨。多元分析很少用于这种类型的数据,对于探索不同 DNA 序列之间的行为相似性和差异性以及对感兴趣 pH 范围内涉及的构象的存在和身份进行建模至关重要。结果表明,对于 i-motif,链内接触的形成和其解离的寿命比 DNA 序列的开放形式快十倍。它们还强调了对于某些 DNA 序列,根据序列的长度和侧环中碱基的组成,存在不止一种 i-motif 物种。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea4d/6649798/cdfbd4f08083/gkz522fig1.jpg

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