Department of Chemistry, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.
Angew Chem Int Ed Engl. 2020 Nov 23;59(48):21488-21492. doi: 10.1002/anie.202009579. Epub 2020 Sep 17.
DNAzymes are widely used as functional units for creating DNA-based sensors and devices. Switching of DNAzyme activity by external stimuli is of increasing interest. Herein we report a Cu -responsive DNAzyme rationally designed by incorporating one of the most stabilizing artificial metallo-base pairs, a Cu -mediated carboxyimidazole base pair (Im -Cu -Im ), into a known RNA-cleaving DNAzyme. Cleavage of the substrate was suppressed without Cu , but the reaction proceeded efficiently in the presence of Cu ions. This is due to the induction of a catalytically active structure by Im -Cu -Im pairing. The on/off ratio was as high as 12-fold, which far exceeds that of the previously reported DNAzyme with a Cu -mediated hydroxypyridone base pair. The DNAzyme activity can be regulated specifically in response to Cu ions during the reaction through the addition, removal, or reduction of Cu . This approach should advance the development of stimuli-responsive DNA systems with a well-defined sharp switching function.
DNA 酶被广泛用作构建基于 DNA 的传感器和设备的功能单元。通过外部刺激来切换 DNA 酶的活性越来越受到关注。本文报道了一种通过将最稳定的人工金属碱基对之一——Cu 介导的羧基咪唑碱基对(Im-Cu-Im)整合到已知的 RNA 切割 DNA 酶中,合理设计的 Cu 响应 DNA 酶。在没有 Cu 的情况下,底物的切割受到抑制,但在 Cu 离子存在下,反应有效地进行。这是由于 Im-Cu-Im 配对诱导了催化活性结构。开/关比值高达 12 倍,远远超过先前报道的具有 Cu 介导的羟吡啶酮碱基对的 DNA 酶。通过添加、去除或还原 Cu,可以在反应过程中特异性地调节 DNA 酶活性以响应 Cu 离子。这种方法应该会推进具有明确锐利切换功能的响应性 DNA 系统的发展。