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首页> 外文期刊>Angewandte Chemie >Transient DNA-Based Nanostructures Controlled by Redox Inputs
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Transient DNA-Based Nanostructures Controlled by Redox Inputs

机译:由氧化还原投入控制的基于瞬时DNA的纳米结构

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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.
机译:合成DNA已成为一种强大的自组装材料,用于纳米级分子器件和材料的工程。 最近,基于DNA的超分子结构的耗散自组装已成为一种新的方法,可进入新类的动力学控制的DNA材料,具有前所未有的寿命性质。 到目前为止,使用DNA识别酶作为能量耗散单元,已经实现了耗散控制。 虽然高效,酶在长期稳定性和抑制废物上的酶活性方面姿态。 在此,我们提供了动力学控制的DNA纳米结构的第一实例,其中通过非酶化学反应实现了能量耗散。 更具体地,通过氧化还原信号传导的启发,我们使用二硫键形成/破裂的氧化还原循环,以便以高度可控和可逆的方式控制管状DNA纳米结构的组装和拆卸。

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