碱基
碱基对
DNA
分子内力
DNA纳米技术
A-DNA
脱氧核酶
纳米技术
金属
基础(拓扑)
鸟嘌呤
粘而钝的末端
材料科学
化学
立体化学
生物化学
核苷酸
数学分析
数学
冶金
基因
作者
Yusuke Takezawa,Keita Mori,Wei-En Huang,Kotaro Nishiyama,Xin Tong,Takao Nakama,Mitsuhiko Shionoya
标识
DOI:10.1038/s41467-023-40353-3
摘要
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 OH ) nucleobase is employed as a metal-responsive unit, forming both a hydrogen-bonded U OH –A base pair and a metal-mediated U OH –Gd III – U OH base pair. Metal-mediated strand displacement reactions are demonstrated under isothermal conditions based on the base-pair switching between U OH –A and U OH –Gd III – U OH . Furthermore, metal-responsive DNA tweezers and allosteric DNAzymes are developed as typical models for DNA nanodevices simply by incorporating U OH 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.
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