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金属介导的 DNA 碱基配对:氢键沃森-克里克碱基对的替代物。

Metal-mediated DNA base pairing: alternatives to hydrogen-bonded Watson-Crick base pairs.

机构信息

Department of Chemistry, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.

出版信息

Acc Chem Res. 2012 Dec 18;45(12):2066-76. doi: 10.1021/ar200313h. Epub 2012 Mar 27.

Abstract

With its capacity to store and transfer the genetic information within a sequence of monomers, DNA forms its central role in chemical evolution through replication and amplification. This elegant behavior is largely based on highly specific molecular recognition between nucleobases through the specific hydrogen bonds in the Watson-Crick base pairing system. While the native base pairs have been amazingly sophisticated through the long history of evolution, synthetic chemists have devoted considerable efforts to create alternative base pairing systems in recent decades. Most of these new systems were designed based on the shape complementarity of the pairs or the rearrangement of hydrogen-bonding patterns. We wondered whether metal coordination could serve as an alternative driving force for DNA base pairing and why hydrogen bonding was selected on Earth in the course of molecular evolution. Therefore, we envisioned an alternative design strategy: we replaced hydrogen bonding with another important scheme in biological systems, metal-coordination bonding. In this Account, we provide an overview of the chemistry of metal-mediated base pairing including basic concepts, molecular design, characteristic structures and properties, and possible applications of DNA-based molecular systems. We describe several examples of artificial metal-mediated base pairs, such as Cu(2+)-mediated hydroxypyridone base pair, H-Cu(2+)-H (where H denotes a hydroxypyridone-bearing nucleoside), developed by us and other researchers. To design the metallo-base pairs we carefully chose appropriate combinations of ligand-bearing nucleosides and metal ions. As expected from their stronger bonding through metal coordination, DNA duplexes possessing metallo-base pairs exhibited higher thermal stability than natural hydrogen-bonded DNAs. Furthermore, we could also use metal-mediated base pairs to construct or induce other high-order structures. These features could lead to metal-responsive functional DNA molecules such as artificial DNAzymes and DNA machines. In addition, the metallo-base pairing system is a powerful tool for the construction of homogeneous and heterogeneous metal arrays, which can lead to DNA-based nanomaterials such as electronic wires and magnetic devices. Recently researchers have investigated these systems as enzyme replacements, which may offer an additional contribution to chemical biology and synthetic biology through the expansion of the genetic alphabet.

摘要

DNA 凭借其在单体序列中存储和传递遗传信息的能力,通过复制和扩增在化学进化中发挥核心作用。这种优雅的行为在很大程度上基于碱基之间通过 Watson-Crick 碱基配对系统中的氢键进行高度特异性的分子识别。虽然天然碱基对在漫长的进化过程中已经变得非常复杂,但合成化学家在最近几十年中投入了相当大的努力来创建替代碱基配对系统。这些新系统中的大多数都是基于碱基对的形状互补或氢键模式的重排设计的。我们想知道金属配位是否可以作为 DNA 碱基配对的替代驱动力,以及在分子进化过程中,为什么氢键会在地球上被选择。因此,我们设想了一种替代设计策略:我们用另一种在生物系统中重要的方案取代氢键,即金属配位键。在本综述中,我们提供了金属介导碱基配对的化学概述,包括基本概念、分子设计、特征结构和性质,以及基于 DNA 的分子系统的可能应用。我们描述了几个人工金属介导碱基对的例子,例如我们和其他研究人员开发的 Cu(2+)-介导的羟吡啶碱基对、H-Cu(2+)-H(其中 H 表示含有羟吡啶碱基的核苷)。为了设计金属碱基对,我们仔细选择了带有配体的核苷和金属离子的合适组合。正如预期的那样,由于通过金属配位形成的更强键,含有金属碱基对的 DNA 双链体比天然氢键 DNA 具有更高的热稳定性。此外,我们还可以使用金属介导的碱基对构建或诱导其他高级结构。这些特性可以导致金属响应性功能 DNA 分子,例如人工 DNA 酶和 DNA 机器。此外,金属碱基配对系统是构建均相和非均相金属阵列的有力工具,可导致基于 DNA 的纳米材料,例如电子线和磁性器件。最近,研究人员将这些系统作为酶替代物进行了研究,这可能通过扩展遗传密码为化学生物学和合成生物学做出额外的贡献。

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