Jin Ye, Ru Xuyan, Su Neil Qiang, Mei Yuncai, Beratan David N, Zhang Peng, Yang Weitao
Department of Chemistry, Duke University, Durham, North Carolina 27708, United States.
Department of Biochemistry, Duke University, Durham, North Carolina 27710, United States.
J Phys Chem B. 2020 Apr 23;124(16):3428-3435. doi: 10.1021/acs.jpcb.0c03112. Epub 2020 Apr 13.
The extent of electronic wave function delocalization for the charge carrier (electron or hole) in double helical DNA plays an important role in determining the DNA charge transfer mechanism and kinetics. The size of the charge carrier's wave function delocalization is regulated by the solvation induced localization and the quantum delocalization among the π stacked base pairs at any instant of time. Using a newly developed localized orbital scaling correction (LOSC) density functional theory method, we accurately characterized the quantum delocalization of the hole wave function in double helical B-DNA. This approach can be used to diagnose the extent of delocalization in fluctuating DNA structures. Our studies indicate that the hole state tends to delocalize among 4 guanine-cytosine (GC) base pairs and among 3 adenine-thymine (AT) base pairs when these adjacent bases fluctuate into degeneracy. The relatively small delocalization in AT base pairs is caused by the weaker π-π interaction. This extent of delocalization has significant implications for assessing the role of coherent, incoherent, or flickering coherent carrier transport in DNA.
双螺旋DNA中电荷载流子(电子或空穴)的电子波函数离域程度在决定DNA电荷转移机制和动力学方面起着重要作用。在任何时刻,电荷载流子波函数的离域大小受溶剂化诱导局域化以及π堆积碱基对之间的量子离域的调节。使用新开发的局域轨道标度校正(LOSC)密度泛函理论方法,我们准确地表征了双螺旋B-DNA中空穴波函数的量子离域。这种方法可用于诊断波动DNA结构中的离域程度。我们的研究表明,当这些相邻碱基波动到简并状态时,空穴态倾向于在4个鸟嘌呤-胞嘧啶(GC)碱基对之间以及3个腺嘌呤-胸腺嘧啶(AT)碱基对之间离域。AT碱基对中相对较小的离域是由较弱的π-π相互作用引起的。这种离域程度对于评估DNA中相干、非相干或闪烁相干载流子传输的作用具有重要意义。