Jackson State University, 1400 J. R. Lynch, Jackson, MS 39217, USA.
J Mol Model. 2013 Sep;19(9):3543-9. doi: 10.1007/s00894-013-1833-9. Epub 2013 May 31.
The study of pre-translational effects (ionization, tautomerization) and post-translational effects (methylation) of adenine and thymine has only recently been the focus of some studies. These effects can potentially help regulate gene expression as well as potentially disrupt normal gene function. Because of this wide array of roles, greater insight into these effects in deoxyribonucleic acids (DNA) are paramount. There has been considerable research of each phenomenon (tautomerization, methylation and ionization) individually. In this work, we attempt to shed light upon the pre-translational effects and post translational effects of adenine and thymine by investigating the electron affinities (EAs) and ionization potentials (IPs) of the major and minor tautomers and their methyl derivatives. We performed all calculations using the density functional theory (DFT) B3LYP functional accompanied with 6-311G(d,p), 6-311+G(d,p) and 6-311++G(df,pd) basis sets. Our results reveal that the thymine tautomer has a higher EA and IP than the adenine tautomers. The higher EA suggests that an electron that attaches to the AT base pair would predominately attach to the thymine instead of adenine. The higher IP would suggest that an electron that is removed from the AT base pair would be predominately removed from the adenine within the base pair. Understanding how tautomerization, ionization and methylation differences change effects, discourages, or promotes one another is lacking. In this work, we begin the steps of integrating these effects with one another, to gain a greater understanding of molecular changes in DNA bases.
腺嘌呤和胸腺嘧啶的翻译前效应(离子化、互变异构)和翻译后效应(甲基化)的研究最近才成为一些研究的焦点。这些效应可能有助于调节基因表达,并可能破坏正常的基因功能。由于这些广泛的作用,深入了解 DNA 中的这些效应至关重要。已经对每种现象(互变异构、甲基化和离子化)进行了相当多的研究。在这项工作中,我们通过研究主要和次要互变异构体及其甲基衍生物的电子亲和能(EAs)和电离势(IPs),试图阐明腺嘌呤和胸腺嘧啶的翻译前效应和翻译后效应。我们使用密度泛函理论(DFT)B3LYP 函数,结合 6-311G(d,p)、6-311+G(d,p)和 6-311++G(df,pd)基组进行了所有计算。我们的结果表明,胸腺嘧啶互变异构体具有比腺嘌呤互变异构体更高的 EA 和 IP。较高的 EA 表明,附着在 AT 碱基对的电子将主要附着在胸腺嘧啶上,而不是腺嘌呤上。较高的 IP 表明,从 AT 碱基对中去除的电子将主要从碱基对中的腺嘌呤中去除。了解互变异构、离子化和甲基化差异如何改变效应、抑制或促进彼此之间的相互作用还很缺乏。在这项工作中,我们开始将这些效应相互结合,以更好地理解 DNA 碱基的分子变化。