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  4. Computational prediction of one-electron oxidation potentials for cytosine and uracil epigenetic derivatives
 
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Computational prediction of one-electron oxidation potentials for cytosine and uracil epigenetic derivatives

Publikationstyp
Journal Article
Date Issued
2025-04-08
Sprache
English
Author(s)
Korotenko, Vasilii 
Thermische Verfahrenstechnik V-8  
Langrzyk, Patrick  
Zipse, Hendrik  
TORE-URI
https://hdl.handle.net/11420/56034
Journal
The journal of physical chemistry A  
Volume
129
Issue
20
Start Page
4339
End Page
4356
Citation
Journal of Physical Chemistry A 129 (20): 4339-4356 (2025)
Publisher DOI
10.1021/acs.jpca.4c06944
Scopus ID
2-s2.0-105002790801
Publisher
American Chemical Society
Knowledge of the redox properties of cytosine (C), uracil (U), and their natural derivatives is essential for a deeper understanding of DNA damage, repair, and epigenetic regulation. This study investigates the one-electron oxidation potential (Eox, V) using DFT (B3LYP-D3) and DLPNO-CCSD(T) methods with explicit/implicit (SMD) solvation model. Calculations in the gas phase and aprotic solvents such as acetonitrile showed a high correlation with experimental data (0.96-0.98). In aqueous solutions at pH 7, oxidation potentials are significantly influenced by deprotonation equilibria, as acidic molecules like 5caC become easier to oxidize upon deprotonation. The resulting oxidation potentials reflect a complex interplay of substituent effects, acidity, and protonation states. A pH-dependent model based on the Nernst equation for aqueous solutions demonstrated a correlation coefficient of 0.93. The calculated E<inf>ox</inf> values for cytosine epigenetic derivatives in water, accounting for deprotonation effects, follow the trend: d_5caC < 5mC < 5caC < 5hmC < C < 5dhmC < 5fC, where “d_” deprotonated, “5ca” 5-carboxy, “5m” 5-methyl, “5hm” 5-hydroxymethyl, “5dhm” 5-dihydroxymethyl, “5f” 5-formyl.
DDC Class
530: Physics
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