Abstract
DNA oligomers can form silver-mediated duplexes, stable in gas phase and solution, with potential for novel biomedical and technological applications. The nucleobase-metal bond primarily drives duplex formation, but hydrogen (H-) bonds may also be important for structure selection and stability. To elucidate the role of H-bonding, we conducted theoretical and experimental studies of a duplex formed by silver-mediated cytosine homopobase DNA strands, two bases long. This silver-mediated cytosine tetramer is small enough to permit accurate, realistic modeling by DFT-based quantum mechanics/molecular mechanics methods. In gas phase, our calculations found two energetically favorable configurations distinguished by H-bonding, one with a novel interplane H-bond, and the other with planar H-bonding of silver-bridged bases. Adding solvent favored silver-mediated tetramers with interplane H-bonding. Overall agreement of electronic circular dichroism spectra for the final calculated structure and experiment validates these findings. Our results can guide use of these stabilization mechanisms for devising novel metal-mediated DNA structures.
| Original language | English |
|---|---|
| Pages (from-to) | 4061-4066 |
| Number of pages | 6 |
| Journal | Journal of Physical Chemistry Letters |
| Volume | 6 |
| Issue number | 20 |
| DOIs | |
| Publication status | Published - 15 Oct 2015 |
| MoE publication type | A1 Journal article-refereed |
Keywords
- argentophilic
- circular dichroism
- density functional theory
- DNA
- metal-organic
- silver cation
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