Silver(I)‐Mediated 2D DNA Nanostructures

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<sup>+</sup>-cytosine (dC:Ag<sup>+</sup>:dC) base pair as a chemical trigger for self-assembly is described. It is demonstrated that Ag<sup>+</sup>-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.

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Publication Details

Journal
Small
Published
2024-11-20
DOI
https://doi.org/10.1002/smll.202407604
Citations
4
Primary Topic
Advanced biosensing and bioanalysis techniques
Type
article
Field-Weighted Citation Impact
0.94

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article

Silver(I)‐Mediated 2D DNA Nanostructures

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4 citations
Small
Advanced biosensing and bioanalysis techniques
0.94
article

Silver(I)‐Mediated 2D DNA Nanostructures

Ruojie Sha, Simon Vecchioni, Lynn J. Rothschild, Shalom J. Wind, Yoel P. Ohayon, Kun Wang, Qiuyan Huang, R. Lo
article en
4 citations

Abstract

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<sup>+</sup>-cytosine (dC:Ag<sup>+</sup>:dC) base pair as a chemical trigger for self-assembly is described. It is demonstrated that Ag<sup>+</sup>-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.

SmallVol. 21(3)
Ames Research Center (US), King's College London (GB), London Cancer (GB), Planetary Systems (United States) (US), Imperial College London (GB), New York University (US), Columbia University (US)
National Science Foundation, U.S. Department of Energy, National Aeronautics and Space Administration, York University, Office of Naval Research, Office of Naval Research Global
Openalex Percentile: Top 25%
Advanced biosensing and bioanalysis techniques
0.94
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