Influence of transition mutations and disorder on charge localization and transfer along B-DNA sequences
Pavlos Banev, Anastasia Falliera, and Constantinos Simserides

TL;DR
This study investigates how transition mutations and disorder affect charge localization and transfer in B-DNA sequences using tight-binding models, revealing that mutations and disorder generally increase localization and impede charge transfer.
Contribution
It introduces a detailed analysis of mutation and disorder effects on charge transfer in B-DNA using advanced tight-binding models and parameters from recent atomic-level studies.
Findings
Transition mutations increase localization and reduce charge transfer.
Disorder significantly increases localization and alters eigenenergies.
Mutated sites with significant parameter changes impede charge transfer.
Abstract
We illuminate the influence of transition mutations and disorder on charge localization and transfer along B-DNA sequences. Homopolymers are the best for charge transfer (cf. Refs.~ \cite{LVBMS:2018, MLTS:2019}). Hence, we consider as flawless a homopolymer sequence and then disturb it, introducing transition mutations and disorder. We exclude the possibility of charge transfer via the backbone that will be addressed soon in another work. We employ the Tight Binding (TB) Wire model to study the influence of transition mutations and the TB Fishbone Wire model to evaluate the influence of disorder emanating either from the path or from the backbone. For the TB Wire parameters, we employ the parametrization created in Ref.~\cite{MLS:2023}, where another TB at atomic level was used, considering all valence orbitals of all atoms. We calculate the HOMO and LUMO regime eigenenergies and…
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