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基于 5-羟尿嘧啶碱基对切换的金属介导 DNA 链置换和分子器件操作。

Metal-mediated DNA strand displacement and molecular device operations based on base-pair switching of 5-hydroxyuracil nucleobases.

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

Nat Commun. 2023 Aug 24;14(1):4759. doi: 10.1038/s41467-023-40353-3.

Abstract

Rational design of self-assembled DNA nanostructures has become one of the fastest-growing research areas in molecular science. Particular attention is focused on the development of dynamic DNA nanodevices whose configuration and function are regulated by specific chemical inputs. Herein, we demonstrate the concept of metal-mediated base-pair switching to induce inter- and intramolecular DNA strand displacement in a metal-responsive manner. The 5-hydroxyuracil (U) nucleobase is employed as a metal-responsive unit, forming both a hydrogen-bonded U-A base pair and a metal-mediated U-Gd-U base pair. Metal-mediated strand displacement reactions are demonstrated under isothermal conditions based on the base-pair switching between U-A and U-Gd-U. Furthermore, metal-responsive DNA tweezers and allosteric DNAzymes are developed as typical models for DNA nanodevices simply by incorporating U bases into the sequence. The metal-mediated base-pair switching will become a versatile strategy for constructing stimuli-responsive DNA nanostructures, expanding the scope of dynamic DNA nanotechnology.

摘要

自组装 DNA 纳米结构的合理设计已成为分子科学中发展最快的研究领域之一。人们特别关注开发动态 DNA 纳米器件,其结构和功能可通过特定的化学输入进行调节。在此,我们展示了一种金属介导的碱基对切换的概念,以诱导金属响应的分子内和分子间 DNA 链置换。5-羟基尿嘧啶 (U) 核苷碱基被用作金属响应单元,形成氢键 U-A 碱基对和金属介导的 U-Gd-U 碱基对。基于 U-A 和 U-Gd-U 之间的碱基对切换,在等温条件下证明了金属介导的链置换反应。此外,通过将 U 碱基纳入序列,开发了金属响应 DNA 镊子和别构 DNA 酶作为 DNA 纳米器件的典型模型。金属介导的碱基对切换将成为构建刺激响应 DNA 纳米结构的通用策略,扩展动态 DNA 纳米技术的范围。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab25/10449808/35fc263be949/41467_2023_40353_Fig1_HTML.jpg

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