Electrochemical Switching with 3D DNA Tetrahedral Nanostructures Self-Assembled at Gold Electrodes

被引:73
作者
Abi, Alireza [1 ,2 ,3 ]
Lin, Meihua [4 ,5 ]
Pei, Hao [4 ,5 ]
Fan, Chunhai [4 ,5 ]
Ferapontova, Elena E. [1 ,2 ]
Zuo, Xiaolei [4 ,5 ]
机构
[1] Aarhus Univ, Interdisciplinary Nanosci Ctr iNANO, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ, iNANO, Ctr DNA Nanotechnol CDNA, DK-8000 Aarhus C, Denmark
[3] Aarhus Univ, iNANO, Sino Danish Ctr Educ & Res SDC, DK-8000 Aarhus C, Denmark
[4] Chinese Acad Sci, Div Phys Biol, Shanghai 201800, Peoples R China
[5] Chinese Acad Sci, CAS Key Lab Interfacial Phys & Technol, Shanghai Inst Appl Phys, Bioimaging Ctr,Shanghai Synchrotron Radiat Facil, Shanghai 201800, Peoples R China
基金
中国国家自然科学基金; 新加坡国家研究基金会;
关键词
DNA nanotechnology; 3D nanostructures; DNA tetrahedron; electromechanical devices; nanomechanical switching; self-assembly; TRANSPORT; DUPLEXES; END; SENSORS;
D O I
10.1021/am501823q
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Nanomechanical switching of functional three-dimensional (3D) DNA nanostructures is crucial for nanobiotechnological applications such as nanorobotics or self-regulating sensor and actuator devices. Here, DNA tetrahedral nanostructures self-assembled onto gold electrodes were shown to undergo the electronically addressable nanoswitching due to their mechanical reconfiguration upon external chemical stimuli. That enables construction of robust surface-tethered electronic nanodevices based on 3D DNA tetrahedra. One edge of the tetrahedron contained a partially self-complementary region with a stem-loop hairpin structure, reconfigurable upon hybridization to a complementary DNA (stimulus DNA) sequence. A non-intercalative ferrocene (Fc) redox label was attached to the reconfigurable tetrahedron edge in such a way that reconfiguration of this edge changed the distance between the electrode and Fc.
引用
收藏
页码:8928 / 8931
页数:4
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