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Proton-Transfer-Steered Mechanism of Photolesion Repair by (6-4)-Photolyases

机译:(6-4)-光解酶修复光子损伤的质子转移机理

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摘要

DNA (6-4)-photolyases are enzymes initiating cleavage of mutagenic pyrimidine (6-4) pyrimidone photo-lesions by a photoinitiated electron transfer from flavin adenine dinucleotide to the lesion. Using state-of-the-art quantum chemical calculations, we present the first energetically feasible molecular repair mechanism. The initial step is electron transfer coupled to proton transfer from the protonated His345 to the N3′ nitrogen of the pyrimidone thymine of the lesion, which proceeds simultaneously with intramolecular OH transfer in a concerted reaction without formation of an oxetane or isolated water molecule intermediate. In contrast to previously suggested mechanisms, this newly identified pathway requires neither a two-photon process nor electronic excitation of the photolesion.Indeed, the recognition that the initial electron transfer is coupled to the proton transfer was critically important for clarification of the mechanism.
机译:DNA(6-4)-光解酶是通过从黄素腺嘌呤二核苷酸向病变的光引发电子转移,引发诱变嘧啶(6-4)嘧啶酮光损伤裂解的酶。使用最新的量子化学计算,我们提出了第一个在能量上可行的分子修复机制。初始步骤是电子转移,与质子从His345质子转移到病灶的嘧啶酮胸腺嘧啶的N3'氮相结合,该转移与分子内OH转移同时进行,并且协调一致,没有形成氧杂环丁烷或分离出的水分子中间体。与先前提出的机制相反,这一新发现的途径既不需要双光子过程也不需要电子激发光损伤。事实上,认识到初始电子转移与质子转移耦合对于阐明机制至关重要。

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