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用于DNA无标记分析的对称曲率描述符。

Symmetric curvature descriptors for label-free analysis of DNA.

作者信息

Buzio Renato, Repetto Luca, Giacopelli Francesca, Ravazzolo Roberto, Valbusa Ugo

机构信息

CNR-SPIN Institute for Superconductors, Innovative Materials and Devices, Genova, Italy.

Department of Physics, University of Genova, Genova, Italy.

出版信息

Sci Rep. 2014 Sep 24;4:6459. doi: 10.1038/srep06459.

Abstract

High-resolution microscopy techniques such as electron microscopy, scanning tunnelling microscopy and atomic force microscopy represent well-established, powerful tools for the structural characterization of adsorbed DNA molecules at the nanoscale. Notably, the analysis of DNA contours allows mapping intrinsic curvature and flexibility along the molecular backbone. This is particularly suited to address the impact of the base-pairs sequence on the local conformation of the strands and plays a pivotal role for investigations relating the inherent DNA shape and flexibility to other functional properties. Here, we introduce novel chain descriptors aimed to characterize the local intrinsic curvature and flexibility of adsorbed DNA molecules with unknown orientation. They consist of stochastic functions that couple the curvatures of two nanosized segments, symmetrically placed on the DNA contour. We show that the fine mapping of the ensemble-averaged functions along the molecular backbone generates characteristic patterns of variation that highlight all pairs of tracts with large intrinsic curvature or enhanced flexibility. We demonstrate the practical applicability of the method for DNA chains imaged by atomic force microscopy. Our approach paves the way for the label-free comparative analysis of duplexes, aimed to detect nanoscale conformational changes of physical or biological relevance in large sample numbers.

摘要

高分辨率显微镜技术,如电子显微镜、扫描隧道显微镜和原子力显微镜,是用于在纳米尺度上对吸附的DNA分子进行结构表征的成熟且强大的工具。值得注意的是,对DNA轮廓的分析能够绘制出沿分子主链的固有曲率和柔韧性。这特别适合于研究碱基对序列对链的局部构象的影响,并且在将DNA固有形状和柔韧性与其他功能特性相关联的研究中起着关键作用。在此,我们引入了新的链描述符,旨在表征取向未知的吸附DNA分子的局部固有曲率和柔韧性。它们由随机函数组成,这些函数将对称放置在DNA轮廓上的两个纳米尺寸片段的曲率耦合起来。我们表明,沿分子主链对系综平均函数进行精细映射会产生特征性的变化模式,突出显示所有具有大固有曲率或增强柔韧性的片段对。我们证明了该方法对原子力显微镜成像的DNA链的实际适用性。我们的方法为双链体的无标记比较分析铺平了道路,旨在检测大量样本中具有物理或生物学相关性的纳米尺度构象变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24bb/5377314/525458d0176c/srep06459-f1.jpg

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