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Reaction path analysis for demethylation process of histone tail lysine residues

机译:组蛋白尾赖氨酸残基脱甲基过程的反应路径分析

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Histone proteins control many crucial cell regulatory processes post-translational modifications. Among these modifications, methylation is recently shown to be reversible with the discovery of Lysine-specific Demethylase (LSD1) enzyme. As many studies have showed the relation of some cancer-type and other diseases with the abnormalities in the balance of methylation/demethylation, drug molecule design based on the information gained from reaction path analysis becomes very useful. In this paper, a chemically-consistent reaction mechanism is proposed for the demethylation of histone tail lysine residues and the reaction path analysis of this mechanism is carried out. Potential and free energy profiles of the system, which does not include the residues of the enzyme, are calculated with semi-empirical and quantum mechanical (QM) methods. These results create a fundamental basis for further analysis of the demethylation process with enzyme and/or inhibitor molecules available in the literature.
机译:组蛋白控制翻译后修饰的许多关键细胞调节过程。在这些修饰中,最近发现赖氨酸特异性脱甲基酶(LSD1)酶可逆甲基化。由于许多研究表明某些癌症类型和其他疾病与甲基化/去甲基化平衡异常之间的关系,基于从反应路径分析获得的信息的药物分子设计变得非常有用。提出了化学一致的组蛋白尾赖氨酸残基脱甲基反应机理,并对该反应机理进行了反应路径分析。使用半经验和量子力学(QM)方法计算系统的势能和自由能分布图,其中不包括酶的残基。这些结果为进一步分析文献中可用的酶和/或抑制剂分子的脱甲基过程奠定了基础。

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