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Chiral multichromophoric supramolecular nanostructures assembled by single stranded DNA and RNA templates

机译:由单链DNA和RNA模板组装的手性多色超分子纳米结构

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A complex and well-organized network of non-covalent bonds (also known as supramolecular interactions) is the foundation of the immense functional and structural diversity of biological systems. Chirality can be found at the center of almost all biological processes as clearly evidenced by the homochirality of the biological world. Stereoselective interactions are responsible for the self assembly of macromolecules, biomolecular recognition, as well as cellular machinery and communication. Non-covalent interactions are also ideally suited for the construction of bio-inspired artificial nanoarchitectures with prescribed properties and functions. Nucleic acids (NAs) proved to be valuable chiral scaffolds for precise arrangement of desired molecular components into chiral, periodically patterned nanosystems. Single stranded NAs (ssDNA and ssRNA) are particularly suitable for templated supramolecular bottom-up nanoassembly. In this review article, we describe the progress in using the homochiral ssDNA and s5RNA as templates to assemble molecular components into chiral double-zipper supramolecular nanostructures via non-covalent interactions (i.e., hydrogen and coordination bonding, electrostatic and 7t-it stacking interactions) and discuss their chiroptical and structural properties. We outline the challenges in controlling the handedness of ssNA templated assemblies as well as challenges in accessing either of two helical geometries using the same ssNA template. We discuss empirical methods and theoretical simulations for determination of the handedness as well as chiroptical and structural properties of templated assemblies. We highlight higher order architectures of chiral ssNA templated nanoassemblies as detected by atomic force and transmission electron microscopies (AFM and TEM). (C) 2017 Elsevier B.V. All rights reserved.
机译:非共价键的复杂且组织良好的网络(也称为超分子相互作用)是生物系统巨大功能和结构多样性的基础。手性几乎可以在所有生物过程的中心发现,生物学世界的同质性清楚地证明了这一点。立体选择性相互作用负责大分子的自组装,生物分子识别以及细胞机械和通信。非共价相互作用也非常适合构建具有规定特性和功能的生物启发型人工纳米建筑。核酸(NAs)被证明是有价值的手性支架,用于将所需分子组分精确排列到手性的,周期性形成图案的纳米系统中。单链NA(ssDNA和ssRNA)特别适用于模板化的超分子自下而上的纳米组装。在这篇综述文章中,我们描述了使用同手性ssDNA和s5RNA作为模板通过非共价相互作用(即氢和配位键,静电和7t-it堆叠相互作用)将分子成分组装成手性双拉链超分子纳米结构的进展。并讨论它们的按摩和结构特性。我们概述了控制ssNA模板化组件的手工性方面的挑战,以及使用同一ssNA模板访问两个螺旋几何体中的任何一个的挑战。我们讨论确定模板组件的惯性以及手性和结构性的经验方法和理论模拟。我们重点介绍了通过原子力和透射电子显微镜(AFM和TEM)检测的手性ssNA模板纳米组件的高阶体系结构。 (C)2017 Elsevier B.V.保留所有权利。

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