The Center for Modeling & Simulation Chemistry, Institute of Theoretical Chemistry, Shandong University, Jinan 250100, People's Republic of China.
J Chem Phys. 2011 Oct 7;135(13):134315. doi: 10.1063/1.3646308.
The effect of double proton transfer (DPT) on charge migration of DNA was investigated by the nonequilibrium Green's function method combined with density functional theory. The results revealed that DPT not only lowers ionization potentials, but also improves the delocalization of the localized π-orbitals at each base moiety through adjusting energy levels and spatial distributions of their molecular orbitals. Furthermore, DPT leads to both the strengthening of the second-order interactions of the Watson-Crick H-bond zones, and the promotion of the charge transfer transitions between two pairing bases in the UV absorption spectra. Electronic transport calculations indicated that DPT can improve the charge migration along the DNA duplex for specific sequences through enhancing transverse base-to-base electronic communication. This work will provide a new insight into the understanding of DNA charge conduction which can be electronically promoted or regulated by DPT.
采用非平衡格林函数方法结合密度泛函理论研究了双质子转移(DPT)对 DNA 电荷迁移的影响。结果表明,DPT 不仅降低了电离势,还通过调整轨道能级和空间分布来改善每个碱基部分的局域π轨道的离域性。此外,DPT 导致 Watson-Crick H 键区的二阶相互作用增强,并且在紫外吸收光谱中促进了两个配对碱基之间的电荷转移跃迁。电子输运计算表明,DPT 可以通过增强横向碱基对碱基的电子通信来提高特定序列 DNA 双链的电荷迁移率。这项工作将为理解 DNA 电荷传导提供新的视角,这种传导可以通过 DPT 进行电子促进或调节。