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通过正交自组装定向形成 DNA 纳米阵列。

Directed formation of DNA nanoarrays through orthogonal self-assembly.

机构信息

School of Chemistry, University of Southampton, Highfield, Southampton SO171BJ, UK.

出版信息

Molecules. 2011 Jun 15;16(6):4912-22. doi: 10.3390/molecules16064912.

Abstract

We describe the synthesis of terpyridine modified DNA strands which selectively form DNA nanotubes through orthogonal hydrogen bonding and metal complexation interactions. The short DNA strands are designed to self-assemble into long duplexes through a sticky-end approach. Addition of weakly binding metals such as Zn(II) and Ni(II) induces the formation of tubular arrays consisting of DNA bundles which are 50-200 nm wide and 2-50 nm high. TEM shows additional long distance ordering of the terpy-DNA complexes into fibers.

摘要

我们描述了通过正交氢键和金属配位相互作用选择性形成 DNA 纳米管的三吡啶基修饰 DNA 链的合成。这些短的 DNA 链被设计成通过粘性末端方法自组装成长的双链体。添加弱结合金属如 Zn(II)和 Ni(II)会诱导由 DNA 束组成的管状阵列的形成,这些 DNA 束的宽度为 50-200nm,高度为 2-50nm。TEM 显示了三吡啶基-DNA 配合物进一步的长程纤维状有序排列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef2f/6264196/3cd7eda194c4/molecules-16-04912-g001.jpg

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