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利用芳基偶氮吡唑扩展用于DNA纳米技术的光开关工具箱。

Expanding the Toolbox of Photoswitches for DNA Nanotechnology Using Arylazopyrazoles.

作者信息

Adam Volker, Prusty Deepak K, Centola Mathias, Škugor Marko, Hannam Jeffrey S, Valero Julián, Klöckner Bernhard, Famulok Michael

机构信息

LIMES Chemical Biology Unit, Universität Bonn, Gerhard-Domagk-Straße 1, 53121, Bonn, Germany.

Max-Planck-Fellowship Group Chemical Biology, Center of Advanced European Studies and Research, Ludwig-Erhard-Allee 2, 53175, Bonn, Germany.

出版信息

Chemistry. 2018 Jan 24;24(5):1062-1066. doi: 10.1002/chem.201705500. Epub 2018 Jan 2.

Abstract

Photoregulation is among the most promising tools for development of dynamic DNA nanosystems, due to its high spatiotemporal precision, biocompatibility, and ease of use. So far, azobenzene and its derivatives have shown high potential in photocontrolling DNA duplex hybridization by light-dependent photoisomerization. Despite many recent advances, obtaining sufficiently high photoswitching efficiency under conditions more suitable for work with DNA nanostructures are challenging. Here we introduce a pair of arylazopyrazoles as new photoswitches for efficient and reversible control of DNA hybridization achieved even at room temperature with a low number of required modifications. Their photophysical properties in the native state and in DNA strands result in near-quantitative isomerization rates by irradiation with UV and orange light. To demonstrate the applicability of these photoswitches, we have successfully applied one of them to open and close a DNA hairpin by light at room temperature.

摘要

由于具有高时空精度、生物相容性和易用性,光调控是开发动态DNA纳米系统最有前景的工具之一。到目前为止,偶氮苯及其衍生物已通过光依赖的光异构化在光控DNA双链杂交中显示出高潜力。尽管最近有许多进展,但在更适合DNA纳米结构工作的条件下获得足够高的光开关效率仍具有挑战性。在这里,我们引入了一对芳基偶氮吡唑作为新的光开关,即使在室温下,只需少量所需修饰就能实现对DNA杂交的高效和可逆控制。它们在天然状态和DNA链中的光物理性质导致通过紫外线和橙光照射实现近定量的异构化速率。为了证明这些光开关的适用性,我们已成功地将其中一个应用于在室温下通过光照打开和关闭一个DNA发夹结构。

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