Quantum Chemical Study of the Enzymatic Repair of T(6-4)C/C(6-4)T UV-Photolesions by DNA Photolyases

被引:6
|
作者
Faraji, Shirin [1 ]
Wirz, Lukas [1 ]
Dreuw, Andreas [1 ]
机构
[1] Heidelberg Univ, Interdisciplinary Ctr Sci Comp, D-69120 Heidelberg, Germany
关键词
DNA repair; photolyases; DNA cleavage; quantum chemical calculations; electron transfer; PLESSET PERTURBATION-THEORY; CONTINUUM SOLVATION MODELS; DIMER RADICAL-ANION; REACTION COORDINATE; CRYSTAL-STRUCTURE; 6-4; PHOTOPRODUCT; EXCITED-STATES; THYMINE DIMER; MECHANISM; ENERGY;
D O I
10.1002/cphc.201300223
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Several strategies have evolved to repair one of the abundant UV radiation-induced damages caused to DNA, namely the mutagenic pyrimidine (6-4) pyrimidone photolesions. DNA (6-4)-photolyases are enzymes repairing these lesions by a photoinitiated electron transfer. An important aspect of a possible repair mechanism is its generality and transferability to different (6-4) lesions. Therefore, previously suggested mechanisms for the repair of the T(6-4)T lesion are here transferred to the T(6-4)C and C(6-4)T lesions and investigated theoretically using quantum chemical methods. Despite the different functional groups of the pyrimidine bases involved, a general valid molecular mechanism was identified, in which the initial step is an electron transfer coupled to a proton transfer from the protonated HIS365 to the N3 nitrogen of the 3 pyrimidine, followed by an intramolecular OH/NH2 transfer in one concerted step, which does not require an oxetane/azetidine or isolated water/ammonia intermediate.
引用
收藏
页码:2817 / 2824
页数:8
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