Sahu Prabhat K, Kuo Chang-Wang, Lee Shyi-Long
Department of Chemistry and Biochemistry, National Chung Cheng University, Chia-Yi, 621 Taiwan.
J Phys Chem B. 2007 Mar 22;111(11):2991-8. doi: 10.1021/jp066856t. Epub 2007 Feb 28.
The existence of DNA adducts bring the danger of carcinogenesis because of mispairing with normal DNA bases. 1,N6-ethenoadenine adducts (epsilonA) and 1,N6-ethanoadenine adducts (EA) have been considered as DNA adducts to study the interaction with thymine, as DNA base. Several different stable conformers for each type of adenine adduct with thymine, [epsilonA(1)-T(I), epsilonA(2)-T(I), epsilonA(3)-T(I) and EA(1)-T(I), EA(2)-T(I), EA(3)-T(I)] and [epsilonA(1)-T(II), epsilonA(2)-T(II), epsilonA(3)-T(II) and EA(1)-T(II), EA(2)-T(II), EA(3)-T(II)], have been considered with regard to their interactions. The differences in their geometrical structures, energetic properties, and hydrogen-bonding strengths have also been compared with Watson-Crick adenine-thymine base pair (A-T). Single-point energy calculations at MP2/6-311++G** levels on B3LYP/6-31+G* optimized geometries have also been carried out to better estimate the hydrogen-bonding strengths. The basis set superposition error corrected hydrogen-bonding strength sequence at MP2/6-311++G**//B3LYP/6-31+G* for the most stable complexes is found to be EA(2)-T(I) (15.30 kcal/mol) > EA(1)-T(II) (14.98 kcal/mol) > EA(3)-T(II) (14.68 kcal/mol) > epsilonA(2)-T(I) (14.54 kcal/mol) > epsilonA(3)-T(II) (14.22 kcal/mol) > epsilonA(3)-T(II) (13.64 kcal/mol) > A-T (13.62 kcal/mol). The calculated reaction enthalpy value for epsilonA(2)-T(I) is 10.05 kcal/mol, which is the highest among the etheno adduct-thymine complexes and about 1.55 kcal/mol more than those obtained for Watson-Crick A-T base pair and the reaction enthalpy value for EA(1)- T(II) is 10.22 kcal/mol, which is highest among the ethano addcut-thymine complexes and about 1.72 kcal/mol more than those obtained for Watson-Crick A-T base pair. The aim of this research is to provide fundamental understanding of adenine adduct and thymine interaction at the molecular level and to aid in future experimental studies toward finding the possible cause of DNA damage.
DNA加合物的存在会因与正常DNA碱基错配而带来致癌风险。1,N6-乙烯腺嘌呤加合物(εA)和1,N6-乙烷腺嘌呤加合物(EA)被视为DNA加合物,用于研究与作为DNA碱基的胸腺嘧啶的相互作用。已考虑了每种腺嘌呤加合物与胸腺嘧啶的几种不同稳定构象,[εA(1)-T(I)、εA(2)-T(I)、εA(3)-T(I) 以及EA(1)-T(I)、EA(2)-T(I)、EA(3)-T(I)] 和 [εA(1)-T(II)、εA(2)-T(II)、εA(3)-T(II) 以及EA(1)-T(II)、EA(2)-T(II)、EA(3)-T(II)],并研究了它们之间的相互作用。还将它们的几何结构、能量性质和氢键强度的差异与沃森-克里克腺嘌呤-胸腺嘧啶碱基对(A-T)进行了比较。在B3LYP/6-31+G优化几何结构的基础上,进行了MP2/6-311++G*水平的单点能量计算,以更好地估计氢键强度。发现最稳定配合物在MP2/6-311++G//B3LYP/6-31+G*水平下经基组叠加误差校正后的氢键强度顺序为:EA(2)-T(I)(15.30千卡/摩尔)> EA(1)-T(II)(14.98千卡/摩尔)> EA(3)-T(II)(14.68千卡/摩尔)> εA(2)-T(I)(14.54千卡/摩尔)> εA(3)-T(II)(14.22千卡/摩尔)> εA(3)-T(II)(13.64千卡/摩尔)> A-T(13.62千卡/摩尔)。εA(2)-T(I)的计算反应焓值为10.05千卡/摩尔,是乙烯基加合物-胸腺嘧啶配合物中最高的,比沃森-克里克A-T碱基对的反应焓值高约1.55千卡/摩尔;EA(1)-T(II)的反应焓值为10.22千卡/摩尔,是乙烷加合物-胸腺嘧啶配合物中最高的,比沃森-克里克A-T碱基对的反应焓值高约1.72千卡/摩尔。本研究的目的是在分子水平上提供对腺嘌呤加合物与胸腺嘧啶相互作用的基本理解,并有助于未来的实验研究,以找出DNA损伤的可能原因。