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通过微妙的功能化增强基于 DNA 的环状氢键罗塞特的协同性。

Strengthened cooperativity of DNA-based cyclic hydrogen-bonded rosettes by subtle functionalization.

机构信息

Departament de Química Inorgànica i Orgànica & IQTCUB, Universitat de Barcelona, Martí i Franquès 1-11, 08028 Barcelona, Spain.

Department of Chemistry and Pharmaceutical Sciences, AIMMS, Vrije Universiteit Amsterdam, De Boelelaan 1108, 1081 HZ Amsterdam, The Netherlands.

出版信息

Org Biomol Chem. 2023 Oct 25;21(41):8403-8412. doi: 10.1039/d3ob01391j.

Abstract

Cooperative effects cause extra stabilization of hydrogen-bonded supramolecular systems. In this work we have designed hydrogen-bonded rosettes derived from a guanine-cytosine Janus-type motif with the aim of finding a monomer that enhances the synergy of supramolecular systems. For this, relativistic dispersion-corrected density functional theory computations have been performed. Our proposal involves a monomer with three hydrogen-bonds pointing in the same direction, which translates into shorter bonds, stronger donor-acceptor interactions, and more attractive electrostatic interactions, thus giving rise to rosettes with strengthened cooperativity. This newly designed rosette has triple the cooperativity found for the naturally occurring guanine quadruplex.

摘要

协同效应导致氢键超分子体系额外稳定。在这项工作中,我们设计了源自鸟嘌呤-胞嘧啶 Janus 型模式的氢键蔷薇花形结构,目的是寻找一种单体来增强超分子体系的协同作用。为此,进行了相对论分散修正密度泛函理论计算。我们的建议涉及一种具有三个指向同一方向氢键的单体,这转化为更短的键、更强的供体-受体相互作用和更具吸引力的静电相互作用,从而产生协同作用增强的蔷薇花形结构。与天然存在的鸟嘌呤四聚体相比,新设计的蔷薇花形结构的协同作用提高了两倍。

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