Electronic promotion effect of double proton transfer on conduction of DNA through improvement of transverse electronic communication of base pairs

被引:15
|
作者
Liu, Haiying [1 ,2 ]
Li, Genqin [1 ]
Zhang, Laibin [1 ]
Li, Jilai [3 ]
Wang, Meishan [4 ]
Bu, Yuxiang [1 ]
机构
[1] Shandong Univ, Ctr Modeling & Simulat Chem, Inst Theoret Chem, Jinan 250100, Peoples R China
[2] Univ Jinan, Sch Phys, Jinan 250022, Peoples R China
[3] Jilin Univ, State Key Lab Theoret & Computat Chem, Changchun 130023, Peoples R China
[4] Ludong Univ, Sch Phys, Yantai 264025, Peoples R China
来源
JOURNAL OF CHEMICAL PHYSICS | 2011年 / 135卷 / 13期
关键词
MOLECULAR-ORBITAL METHODS; EXPANDED GUANINE ANALOGS; CHARGE-TRANSFER; DENSITY FUNCTIONALS; EXCITED-STATES; BASIS-SETS; TRANSPORT; ADENINE; APPROXIMATION; RESISTANCE;
D O I
10.1063/1.3646308
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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 pi-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. (C) 2011 American Institute of Physics. [doi:10.1063/1.3646308]
引用
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页数:11
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