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一项使用4螺旋、8螺旋和12螺旋DNA纳米结构对DNA管形成机制的研究。

A study of DNA tube formation mechanisms using 4-, 8-, and 12-helix DNA nanostructures.

作者信息

Ke Yonggang, Liu Yan, Zhang Junping, Yan Hao

机构信息

Department of Chemistry and Biochemistry, Arizona State University, Tempe, 85287, USA.

出版信息

J Am Chem Soc. 2006 Apr 5;128(13):4414-21. doi: 10.1021/ja058145z.

Abstract

This paper describes the design and characterization of a new family of rectangular-shaped DNA nanostructures (DNA tiles) containing 4, 8, and 12 helices. The self-assembled morphologies of the three tiles were also investigated. The motivation for designing this set of DNA nanostructures originated from the desire to produce DNA lattices containing periodic cavities of programmable dimensions and to investigate the mechanism of DNA tube formation. Nine assembly scenarios have been investigated through the combination of the three different tiles and three sticky end association strategies. Imaging by atomic force microscopy (AFM) revealed self-assembled structures with varied cavity sizes, lattice morphologies, and orientations. Six samples show only tube formation, two samples show both 2D lattices (>2 microm) and tubes, and one sample shows only 2D lattices without tubes. We found that a lower tile dimensional anisotropy, weaker connection, and corrugated design favor the large 2D array formation, while the opposite (higher tile anisotropy, stronger connection, and uncorrugated design) favors tube formation. We discuss these observations in terms of an energy balance at equilibrium and the kinetic competition between diffusion-limited lateral lattice growth versus fluctuation of the lattice to form tubes at an early stage of the assembly. The DNA nanostructures and their self-assembly demonstrated herein not only provide a new repertoire of scaffolds to template the organization of nanoscale materials, but may also provide useful information for investigating other self-assembly systems.

摘要

本文描述了一种包含4条、8条和12条螺旋的新型矩形DNA纳米结构(DNA瓦片)家族的设计与表征。还研究了这三种瓦片的自组装形态。设计这组DNA纳米结构的动机源于想要制备具有可编程尺寸的周期性空腔的DNA晶格,并研究DNA管形成的机制。通过将三种不同的瓦片与三种粘性末端结合策略相结合,研究了九种组装方案。原子力显微镜(AFM)成像揭示了具有不同空腔尺寸、晶格形态和取向的自组装结构。六个样品仅显示管的形成,两个样品同时显示二维晶格(>2微米)和管,一个样品仅显示没有管的二维晶格。我们发现,较低的瓦片尺寸各向异性、较弱的连接和波纹设计有利于形成大的二维阵列,而相反的情况(较高的瓦片各向异性、较强的连接和无波纹设计)则有利于管的形成。我们从平衡时的能量平衡以及组装早期扩散限制的横向晶格生长与晶格波动形成管之间的动力学竞争方面讨论了这些观察结果。本文展示的DNA纳米结构及其自组装不仅提供了一套新的支架来模板化纳米级材料的组织,还可能为研究其他自组装系统提供有用的信息。

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