霍利迪路口
补骨脂素
胸腺嘧啶
DNA
立体化学
碱基对
分子内力
化学
复式(建筑)
加合物
序列(生物学)
晶体结构
结晶学
生物物理学
生物
DNA修复
生物化学
有机化学
作者
Brandt F. Eichman,Blaine H. M. Mooers,Marie Alberti,John E. Hearst,P Shing Ho
标识
DOI:10.1006/jmbi.2001.4567
摘要
The single-crystal structures are presented for two DNA sequences with the thymine bases covalently cross-linked across the complementary strands by 4'-hydroxymethyl-4,5',8-trimethylpsoralen (HMT). The HMT-adduct of d(CCGCTAGCGG) forms a psoralen-induced Holliday junction, showing for the first time the effect of this important class of chemotheraputics on the structure of the recombination intermediate. In contrast, HMT-d(CCGGTACCGG) forms a sequence-dependent junction. In both structures, the DNA duplex is highly distorted at the thymine base linked to the six-member pyrone ring of the drug. The psoralen cross-link defines the intramolecular interactions of the drug-induced junction, while the sequence-dependent structure is nearly identical to the native Holliday junction of d(CCGGTACCGG) alone. The two structures contrast the effects of drug- and sequence-dependent interactions on the structure of a Holliday junction, suggesting a role for psoralen in the mechanism to initiate repair of psoralen-lesions in mammalian DNA.
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