S-adenosyl-L-methionine analogs as enhanced methyl donors: Towards novel epigenetic regulators

被引:7
|
作者
Jerbi, Jihene [1 ]
Springborg, Michael [1 ,2 ]
den-Haan, Helena [3 ]
Ceron-Carrasco, Jose P. [3 ]
机构
[1] Saarland Univ, Phys & Theoret Chem, D-66123 Saarbrucken, Germany
[2] Tianjin Univ, Sch Mat Sci & Engn, Tianjin 300072, Peoples R China
[3] Univ Catolica San Antonio Murcia UCAM, Comp Engn Dept, Bioinformat & High Performance Comp Res Grp BIO H, Campus Jeronimos, Murcia 30107, Spain
关键词
DNA; Mutations; Methylation; Molecular dynamics; Ab initio; DNA METHYLATION; ADENOSYLMETHIONINE; INHIBITORS; DYNAMICS; MECHANISM; DEMETHYLATION; CYTOSINE; DOCKING; DNMT1;
D O I
10.1016/j.cplett.2017.10.042
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
Many efforts have been devoted to discover molecules able to halt methylation processes in DNA. However, less is known about the application of methyl promoters in the framework of hypomethylation diseases. Herein, we used molecular dynamics and ab initio calculations to assess the methylation ability of the parent S-adenosyl-L-methionine cofactor (SAM) and a series of analogues. Two molecules deposited in the PubChem database are shown to be promising candidates for increasing the methyl transfer rate of the original SAM. The reported data might be consequently used to guide further steps into the search of more efficient methyl donor-based drugs. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:74 / 81
页数:8
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