Structural Basis for Inhibition of the Fat Mass and Obesity Associated Protein (FTO)

被引:131
|
作者
Aik, WeiShen [1 ]
Demetriades, Marina [1 ]
Hamdan, Muhammad K. K. [1 ]
Bagg, Eleanor. A. L. [1 ]
Yeoh, Kar Kheng [1 ]
Lejeune, Clarisse [1 ]
Zhang, Zhihong [1 ]
McDonough, Michael A. [1 ]
Schofield, Christopher J. [1 ]
机构
[1] Univ Oxford, Chem Res Lab, Oxford OX1 3TA, England
关键词
LEADS; GENE; RNA; SUBSTRATE; POSITION; HYPOXIA; DOMAIN;
D O I
10.1021/jm400193d
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The fat mass and obesity associated protein (FTO) is a potential target for anti-obesity medicines. FTO is a 2-oxoglutarate (2OG)-dependent N-methyl nucleic acid demethylase that acts on substrates including 3-methylthymidine, 3-methyluracil, and 6-methyladenine. To identify FTO inhibitors, we screened a set of 2OG analogues and related compounds using differential scanning fluorometry- and liquid chromatography-based assays. The results revealed sets of both cyclic and acyclic 2OG analogues that are FTO inhibitors. Identified inhibitors include small molecules that have been used in clinical studies for the inhibition of other 2OG oxygenases. Crystallo-graphic analyses reveal inhibition by 2OG cosubstrate or primary substrate competitors as well as compounds that bind across both cosubstrate and primary substrate binding sites. The results will aid the development of more potent and selective FTO inhibitors.
引用
收藏
页码:3680 / 3688
页数:9
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