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Atomic-scale determination of DNA conformational response to strained furanose: A static mode approach

机译:应变规模的呋喃糖的DNA构象反应的原子规模确定:静态模式方法。

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摘要

An original approach of macromolecular 'induced-fit' flexibility, namely the static modes, is applied to shed light on some fundamental mechanisms impacting DNA conformations. We first investigate a constrained nucleic acid of the D-CNA family, in which some backbone torsional angles are conformationally restricted by a dioxaphosphorinane ring structure. We take a special interest in α,β-D-CNA, in which α and β angles are restricted to the canonical conformation. We used the static mode method to evaluate the impact of the insertion of modified nucleotides on the stability of DNA/DNA and DNA/RNA duplexes. Although our approach authorizes the design of complex excitation modes on a specific molecule, we here establish with an atomic precision how a DNA south to north transition can be optimally operated through C5′ and O5′ single excitations.
机译:大分子“诱导拟合”灵活性的原始方法,即静态模式,用于阐明影响DNA构象的一些基本机制。我们首先研究D-CNA家族的受约束的核酸,其中一些骨架扭转角在构象上受到二氧杂膦环结构的限制。我们对α,β-D-CNA特别感兴趣,其中α和β角度仅限于规范构象。我们使用静态模式方法评估修饰核苷酸的插入对DNA / DNA和DNA / RNA双链体稳定性的影响。尽管我们的方法授权了对特定分子的复杂激发模式的设计,但我们在此以原子精度确定了如何通过C5'和O5'单激发最佳地操作DNA从南向北的转变。

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