Physicochemical Mechanism of Light-Driven DNA Repair by (6-4) Photolyases

被引:38
作者
Faraji, Shirin [1 ]
Dreuw, Andreas [1 ]
机构
[1] Heidelberg Univ, Interdisciplinary Ctr Sci Comp, D-69120 Heidelberg, Germany
来源
ANNUAL REVIEW OF PHYSICAL CHEMISTRY, VOL 65 | 2014年 / 65卷
关键词
DNA photolyase; pyrimidine dimer; (6-4) photolesion; excited states; electron transfer; proton transfer; CYCLOBUTANE PYRIMIDINE DIMER; ACTIVE-SITE HISTIDINES; ELECTRON-TRANSFER; THYMINE DIMER; CRYSTAL-STRUCTURE; ENERGY-TRANSFER; ULTRAFAST DYNAMICS; PHOTOLESION REPAIR; PHOTOPRODUCT; COFACTOR;
D O I
10.1146/annurev-physchem-040513-103626
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
DNA photolyases are light-activated enzymes that repair DNA damage induced by ultraviolet (UV) radiation. UV radiation causes two of the most abundant mutagenic and cytotoxic DNA lesions: cyclobutane pyrimidine dimers and 6-4 photolesions. Photolyases selectively bind to DNA and initiate the splitting of mutagenic pyrimidine dimers via photoinduced electron transfer from a flavin adenine dinucleotide anion (FADH(-)) to the lesion triggering its repair. This review discusses the consecutive steps of the repair process, from both experimental and theoretical points of view. It covers the following issues: the process of how photolyases accommodate the lesion into their binding pockets, excitation energy transfer between two involved catalytic cofactors, photoinduced electron transfer to the lesion, the splitting of the pyrimidine dimer radical anion, and the fate of the unstable radical species created after the splitting of the thymine dimer. In particular, mechanisms of the splitting and restoration of the original bases are described in detail, and the most probable repair pathways are outlined.
引用
收藏
页码:275 / 292
页数:18
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