Framework Nucleic Acid-Enabled Programming of Electrochemical Catalytic Properties of Artificial Enzymes

被引:20
作者
Zeng, Dongdong [2 ]
San, Lili [1 ]
Qian, Fengyu [2 ]
Ge, Zhilei [3 ]
Xu, Xiaohui [2 ]
Wang, Bin [2 ]
Li, Qian [3 ]
He, Guifang [1 ]
Mi, Xianqiang [1 ,4 ]
机构
[1] Chinese Acad Sci, Shanghai Adv Res Inst, Shanghai 201210, Peoples R China
[2] Shanghai Univ Med & Hlth Sci, Shanghai Key Lab Mol Imaging, Shanghai 201318, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Microsyst & Informat Technol, Key Lab Funct Mat Informat, Shanghai 200050, Peoples R China
关键词
framework nucleic acid; DNA tetrahedral nanostructure; G-quadruplex; electrochemistry; enzymatic activity; DNA; NANOSTRUCTURES; SENSOR; STEP;
D O I
10.1021/acsami.9b06480
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The creation and engineering of artificial enzymes remain a challenge, especially the arrangement of enzymes into geometric patterns with nanometer precision. In this work, we fabricated a series of novel DNA-tetrahedron-scaffolded-DNAzymes (Tetrazymes) and evaluated the catalytic activity of these Tetrazymes by electrochemistry. Tetrazymes were constructed by precisely positioning G-quadruplex on different sites of a DNA tetrahedral framework, with hemin employed as the co-catalyst. Immobilization of Tetrazymes on a gold electrode surface revealed horseradish peroxidase (HPR)-mimicking bioelectrocatalytic property. Cyclic voltammogram and amperometry were employed to evaluate the capability of Tetrazymes of different configurations to electrocatalyze the reduction of hydrogen peroxide (H2O2). These artificial Tetrazymes displayed 6- to 14-fold higher enzymatic activity than G-quadruplex/hemin (G4-hemin) without the DNA tetrahedron scaffold, demonstrating application potential in developing novel G-quadruplex-based electrochemical sensors.
引用
收藏
页码:21859 / 21864
页数:6
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