Transient DNA-Based Nanostructures Controlled by Redox Inputs

被引:51
|
作者
Del Grosso, Erica [1 ]
Prins, Leonard J. [2 ]
Ricci, Francesco [1 ]
机构
[1] Univ Roma Tor Vergata, Dept Chem, Via Ric Sci, I-00133 Rome, Italy
[2] Univ Padua, Dept Chem Sci, Via Marzolo 1, I-35131 Padua, Italy
基金
欧洲研究理事会;
关键词
DNA nanotechnology; DNA structures; nonequilibrium processes; self-assembly; supramolecular chemistry; ASSEMBLIES; DESIGN; DRIVEN; STATE; POLYMERS; RELEASE; BINDING; TILES;
D O I
10.1002/anie.202002180
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Synthetic DNA has emerged as a powerful self-assembled material for the engineering of nanoscale supramolecular devices and materials. Recently dissipative self-assembly of DNA-based supramolecular structures has emerged as a novel approach providing access to a new class of kinetically controlled DNA materials with unprecedented life-like properties. So far, dissipative control has been achieved using DNA-recognizing enzymes as energy dissipating units. Although highly efficient, enzymes pose limits in terms of long-term stability and inhibition of enzyme activity by waste products. Herein, we provide the first example of kinetically controlled DNA nanostructures in which energy dissipation is achieved through a non-enzymatic chemical reaction. More specifically, inspired by redox signalling, we employ redox cycles of disulfide-bond formation/breakage to kinetically control the assembly and disassembly of tubular DNA nanostructures in a highly controllable and reversible fashion.
引用
收藏
页码:13238 / 13245
页数:8
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