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由三种可重复使用的砖状单链DNA瓦片组装而成的尺寸可控的DNA纳米带。

Size-controllable DNA nanoribbons assembled from three types of reusable brick single-strand DNA tiles.

作者信息

Shi Xiaolong, Chen Congzhou, Li Xin, Song Tao, Chen Zhihua, Zhang Zheng, Wang Yanfeng

机构信息

Key Laboratory of Image Information Processing and Intelligent Control, School of Automation, Huazhong University of Science and Technology, Wuhan, 430074, Hubei, China.

Department of Obstetrics and Gynecology, Renmin Hospital of Wuhan University, Wuhan 430060, Hubei, China.

出版信息

Soft Matter. 2015 Nov 21;11(43):8484-92. doi: 10.1039/c5sm00796h.

Abstract

Precise control of nanostructure is a significant goal shared by supramolecular chemistry, nanotechnology and materials science. In DNA nanotechnology, methods of constructing desired DNA nanostructures using programmable DNA strands have been studied extensively and have become a promising branch of research, but developing universal and low-cost (in the sense of using fewer types of DNA strands) methods remains a challenge. In this work, we propose a novel approach to assemble size-controllable DNA nanoribbons with three types of reusable brick SSTs (single-stranded DNA tiles), where the control of ribbon size is achieved by regulating the concentration ratio between manipulative strands and packed single-stranded DNA tiles. In our method, three types of brick SSTs are sufficient in assembling DNA nanoribbons of different sizes, which is much less than the number of types of unique tile-programmable assembling strategy, thus achieving a universal and low-cost method. The assembled DNA nanoribbons are observed and analyzed by atomic force microscopy (AFM). Experimental observations strongly suggest the feasibility and reliability of our method.

摘要

纳米结构的精确控制是超分子化学、纳米技术和材料科学共同追求的重要目标。在DNA纳米技术中,利用可编程的DNA链构建所需DNA纳米结构的方法已得到广泛研究,并成为一个有前景的研究分支,但开发通用且低成本(从使用更少种类的DNA链的意义上来说)的方法仍然是一项挑战。在这项工作中,我们提出了一种新颖的方法,用三种可重复使用的砖块状单链DNA片段(SSTs)组装尺寸可控的DNA纳米带,其中通过调节操纵链与堆积的单链DNA片段之间的浓度比来实现对纳米带尺寸的控制。在我们的方法中,三种类型的砖块状SSTs足以组装不同尺寸的DNA纳米带,这比独特的瓦片可编程组装策略所需的片段种类数量少得多,从而实现了一种通用且低成本的方法。通过原子力显微镜(AFM)对组装好的DNA纳米带进行观察和分析。实验观察结果有力地证明了我们方法的可行性和可靠性。

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