| Literature DB >> 32272019 |
Ye Jin1, Xuyan Ru1, Neil Qiang Su1, Yuncai Mei1, David N Beratan1,2,3, Peng Zhang1, Weitao Yang1.
Abstract
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.Entities:
Year: 2020 PMID: 32272019 PMCID: PMC7456463 DOI: 10.1021/acs.jpcb.0c03112
Source DB: PubMed Journal: J Phys Chem B ISSN: 1520-5207 Impact factor: 2.991