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Identification of novel inhibitors of histone acetyltransferase hMOF through high throughput screening

  • Rukang Zhang
  • , Jiang Wang
  • , Liang Zhao
  • , Shien Liu
  • , Daohai Du
  • , Hong Ding
  • , Shijie Chen
  • , Liyan Yue
  • , Yu Chih Liu
  • , Chenhua Zhang
  • , Hong Liu*
  • , Cheng Luo
  • *此作品的通讯作者

科研成果: 期刊稿件文章同行评审

摘要

The histone acetyltransferases (HATs) in mammals include GCN5 N-acetyltransferases, the MOZ, YBF2, SAS2, and TIP60 proteins, and the orphan HATs. The males absent on the first (MOF) is mainly related to acetylation of histone H4 Lys16 and has influence on downstream genes expression. However, the only inhibitor MG149 presented low activity against MOF. Besides, there was no high throughput screening platform on MOF, which limited the inhibitor discovery and functional study. In our study, we set up a high throughput screening platform based on amplified luminescent proximity homogeneous assay (ALPHA), which led us to a moderate inhibitor DC_M01. By chemical modification, we found DC_M01_7, which was the analog of DC_M01 with an IC50 value of 6 μM. DC_M01_7 significantly inhibited HCT116 cells proliferation and could also inhibit histone 4 lysine 16 acetylation in HCT116 cells. To sum up, our work will probably assist the further development of more potent MOF inhibitors and the functional study of hMOF.

源语言英语
页(从-至)867-876
页数10
期刊European Journal of Medicinal Chemistry
157
DOI
出版状态已出版 - 5 9月 2018
已对外发布

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