Redox-Switchable Binding Properties of the ATP-Aptamer

被引:59
作者
Biniuri, Yonatan [1 ]
Luo, Guo-Feng [1 ]
Fadeev, Michael [1 ]
Wulf, Verena [1 ]
Willner, Itamar [1 ]
机构
[1] Hebrew Univ Jerusalem, Inst Chem, Minerva Ctr Biohybrid Complex Syst, IL-91904 Jerusalem, Israel
基金
以色列科学基金会;
关键词
DNA-APTAMER; IN-VITRO; RNA; RELEASE; MOLECULES; ADENOSINE; SELECTION; THROMBIN; DOCKING; SENSORS;
D O I
10.1021/jacs.9b06256
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, we report on a redox-controllable and reversible complete "ON"/"OFF"-switchable aptamer binding to ATP. A series of methylene blue-modified ATP-aptamers was synthesized, revealing improved binding affinities toward ATP as compared to the nonmodified aptamer. These binding affinities were dependent on the conjugation site of the redox label on the aptamer scaffold. Importantly, we find that the oxidized methylene blue-modified aptamers bind to ATP with micromolar affinity, while the reduced form lacks binding affinity toward ATP, resulting in an unprecedented complete "ON"/"OFF" redox- controllable aptamer switch. We demonstrate the cyclic "ON"/"OFF" binding of ATP to the methylene blue-functionalized aptamer through cyclic oxidation and reduction of the redox label using both chemical and electrochemical means. Molecular dynamics and docking simulations were performed to account for the redox-switchable properties of the conjugated aptamers and to rationalize the enhanced binding affinities of the different aptamer designs.
引用
收藏
页码:15567 / 15576
页数:10
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