S.C. Nanobiotecnologie, National Institute for Cancer Research IST, Genova, Italy.
Nucleic Acids Res. 2012 Jun;40(11):e84. doi: 10.1093/nar/gks210. Epub 2012 Mar 8.
We propose a method for the characterization of the local intrinsic curvature of adsorbed DNA molecules. It relies on a novel statistical chain descriptor, namely the ensemble averaged product of curvatures for two nanosized segments, symmetrically placed on the contour of atomic force microscopy imaged chains. We demonstrate by theoretical arguments and experimental investigation of representative samples that the fine mapping of the average product along the molecular backbone generates a characteristic pattern of variation that effectively highlights all pairs of DNA tracts with large intrinsic curvature. The centrosymmetric character of the chain descriptor enables targetting strands with unknown orientation. This overcomes a remarkable limitation of the current experimental strategies that estimate curvature maps solely from the trajectories of end-labeled molecules or palindromes. As a consequence our approach paves the way for a reliable, unbiased, label-free comparative analysis of bent duplexes, aimed to detect local conformational changes of physical or biological relevance in large sample numbers. Notably, such an assay is virtually inaccessible to the automated intrinsic curvature computation algorithms proposed so far. We foresee several challenging applications, including the validation of DNA adsorption and bending models by experiments and the discrimination of specimens for genetic screening purposes.
我们提出了一种用于描述吸附 DNA 分子局部固有曲率的方法。它依赖于一种新颖的统计链描述符,即对称放置在原子力显微镜成像链轮廓上的两个纳米尺寸片段的曲率乘积的集合平均值。通过理论论证和对代表性样本的实验研究,我们证明了沿着分子主链精细映射平均乘积会产生一种特征变化模式,有效地突出了所有具有大固有曲率的 DNA 片段对。链描述符的中心对称性质使得能够靶向具有未知取向的链。这克服了当前实验策略的一个显著限制,即仅从末端标记分子或回文的轨迹估计曲率图。因此,我们的方法为可靠、无偏、无标记的弯曲双链比较分析铺平了道路,旨在以大量样本检测物理或生物学相关的局部构象变化。值得注意的是,这种检测方法对于迄今为止提出的自动固有曲率计算算法来说几乎是无法实现的。我们预计会有一些具有挑战性的应用,包括通过实验验证 DNA 吸附和弯曲模型,以及用于遗传筛选目的的样本鉴别。