One-Electron Oxidation Potentials and Hole Delocalization in Heterogeneous Single-Stranded DNA.
Jesús Lucia-TamudoManuel AlcamíSergio Diaz-TenderoJuan J NogueiraPublished in: Biochemistry (2023)
The study of DNA processes is essential to understand not only its intrinsic biological functions but also its role in many innovative applications. The use of DNA as a nanowire or electrochemical biosensor leads to the need for a deep investigation of the charge transfer process along the strand as well as of the redox properties. In this contribution, the one-electron oxidation potential and the charge delocalization of the hole formed after oxidation are computationally investigated for different heterogeneous single-stranded DNA strands. We have established a two-step protocol: (i) molecular dynamics simulations in the frame of quantum mechanics/molecular mechanics (QM/MM) were performed to sample the conformational space; (ii) energetic properties were then obtained within a QM1/QM2/continuum approach in combination with the Marcus theory over an ensemble of selected geometries. The results reveal that the one-electron oxidation potential in the heterogeneous strands can be seen as a linear combination of that property within the homogeneous strands. In addition, the hole delocalization between different nucleobases is, in general, small, supporting the conclusion of a hopping mechanism for charge transport along the strands. However, charge delocalization becomes more important, and so does the tunneling mechanism contribution, when the reducing power of the nucleobases forming the strand is similar. Moreover, charge delocalization is slightly enhanced when there is a correlation between pairs of some of the interbase coordinates of the strand: twist/shift, twist/slide, shift/slide, and rise/tilt. However, the internal structure of the strand is not the predominant factor for hole delocalization but the specific sequence of nucleotides that compose the strand.
Keyphrases
- solar cells
- molecular dynamics simulations
- single molecule
- circulating tumor
- electron transfer
- cell free
- nucleic acid
- hydrogen peroxide
- gold nanoparticles
- epithelial mesenchymal transition
- randomized controlled trial
- atomic force microscopy
- binding protein
- circulating tumor cells
- human health
- quantum dots
- ionic liquid
- genome wide
- room temperature
- label free
- risk assessment
- mass spectrometry
- simultaneous determination
- high speed