Silver(I)-Mediated 2D DNA Nanostructures

被引:1
|
作者
Vecchioni, Simon [1 ,2 ]
Lo, Rainbow [3 ,4 ]
Huang, Qiuyan [2 ]
Wang, Kun [2 ]
Ohayon, Yoel P. [2 ]
Sha, Ruojie [2 ]
Rothschild, Lynn J. [5 ]
Wind, Shalom J. [6 ]
机构
[1] Columbia Univ, Dept Biomed Engn, New York, NY 10027 USA
[2] NYU, Dept Chem, New York, NY 10003 USA
[3] Kings Coll London, Comprehens Canc Ctr, Sch Canc & Pharmaceut Sci, Imaging Therapies & Canc Grp, London SE1 1UL, England
[4] Imperial Coll London, Dept Chem, Mol Sci Res Hub, London W12 0BZ, England
[5] NASA, Planetary Syst Branch, Ames Res Ctr, Moffett Field, CA 94035 USA
[6] Columbia Univ, Dept Appl Phys & Appl Math, New York, NY 10027 USA
基金
美国国家科学基金会;
关键词
Ag+; cytosine; DNA nanotechnology; guanine tetraplex; nanomaterials; CHARGE-TRANSPORT; BASE-PAIRS; DUPLEX DNA; METAL; CONDUCTANCE; ORIGAMI; ION; MOLECULES; JUNCTIONS; BINDING;
D O I
10.1002/smll.202407604
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Structural DNA nanotechnology enables the self-organization of matter at the nanometer scale, but approaches to expand the inorganic and electrical functionality of these scaffolds remain limited. Developments in nucleic acid metallics have enabled the incorporation of site-specific metal ions in DNA duplexes and provide a means of functionalizing the double helix with atomistic precision. Here a class of 2D DNA nanostructures that incorporate the cytosine-Ag+-cytosine (dC:Ag+:dC) base pair as a chemical trigger for self-assembly is described. It is demonstrated that Ag+-functionalized DNA can undergo programmable assembly into large arrays and rings, and can be further coassembled with guanine tetraplexes (G4). It is shown that 2D DNA lattices can be assembled with a variety of embedded nanowires at tunable spacing. These results serve as a foundation for further development of self-assembled, metalated DNA nanostructures, with potential for high-precision DNA nanoelectronics with nanometer pitch.
引用
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页数:11
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