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Updated: Feb 3, 2026

Chemical Dimerization-Induced Protein Condensates on Telomeres
Published on: April 12, 2021
The effect of DNA backbone on the triplet mechanism of UV-induced thymine-thymine (6-4) dimer formation
Xingyong Wang1,2, Haibo Yu3,4,5
1School of Chemistry and Molecular Bioscience, University of Wollongong, Wollongong, NSW, 2522, Australia. xingyong@uow.edu.au.
Abstract:
Density functional theory calculations were carried out to investigate the formation mechanism of the thymine-thymine (6-4) dimer ((6-4)TT), which is one of the main DNA lesions induced by ultraviolet radiation and is closely related to skin cancers. The DNA backbone was found to have nonnegligible effects on the triplet reaction pathway, particularly the reaction steps involving substantial base rotations. The mechanism for the isomerization from (6-4)TT to its Dewar valence isomer (DewarTT) was also explored, confirming the necessity of absorbing a second photon. In addition, the solvation effects were examined and showed considerable influence on the potential energy surface. Graphical Abstract DFT calculations on the influence of DNA backbone on the mechanism of UV-induced thymine-thymine (6-4) dimer formation.
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