Construction of Artificial DNAs Containing a Metal Complex-Type Base Pair

M. Shionoya, Kentaro Tanaka
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Abstract

A number of strategies have been so far employed for modifying the periphery of DNA with metal complexes. However, little has been done to explore the DNA core . Recently, we envisioned the use of charged or uncharged metal complexes as replacement building blocks in the interior of the DNA helix. Replacement of the hydrogen-bonded base pairing of natural DNA by alternative base pairing modes is expected to lead not only to expansion of the genetic alphabet but also to novel DNA structures and functions based on the controlled and periodic spacing of the building blocks along the helix axis. This paper provides a summary of our recent progress devoted to the introduction of metal-assisted base pairs directed towards what we term the nano-assembly of metals into the DNA core . Specifically, we detail here syntheses of artificial /3-C-nucleosides bearing a chelator nucleobase (o-phenylenediamine, catechol, 2-aminophenol, pyridine, or hydroxypyridone , and so on), their metal coordination properties with metal ions, and the incorporation of these building blocks into DNA oligomers . The present results raise the appealing possibility that this approach could lead eventually to a novel molecular architecture-type approach to the nano-assembly of multi-metal arrays .
含金属络合型碱基对的人工dna的构建
到目前为止,已经采用了许多策略来用金属配合物修饰DNA的外围。然而,对DNA核心的探索却很少。最近,我们设想使用带电或不带电的金属配合物作为DNA螺旋内部的替代构建块。用其他碱基配对模式取代天然DNA的氢键碱基配对,不仅会导致遗传字母表的扩展,而且还会导致基于螺旋轴上构建块的可控和周期性间距的新的DNA结构和功能。本文总结了我们最近致力于引入金属辅助碱基对的进展,我们称之为金属纳米组装到DNA核心。具体来说,我们在这里详细介绍了带有螯合核碱基的人工/3- c核苷的合成(邻苯二胺、儿茶酚、2-氨基酚、吡啶或羟吡啶酮等),它们与金属离子的金属配位特性,以及这些构建块与DNA低聚物的结合。目前的结果提出了一种吸引人的可能性,即这种方法最终可能导致一种新的分子结构型方法来实现多金属阵列的纳米组装。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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