TY - JOUR
T1 - Identification of novel inhibitors of histone acetyltransferase hMOF through high throughput screening
AU - Zhang, Rukang
AU - Wang, Jiang
AU - Zhao, Liang
AU - Liu, Shien
AU - Du, Daohai
AU - Ding, Hong
AU - Chen, Shijie
AU - Yue, Liyan
AU - Liu, Yu Chih
AU - Zhang, Chenhua
AU - Liu, Hong
AU - Luo, Cheng
N1 - Publisher Copyright:
© 2018
PY - 2018/9/5
Y1 - 2018/9/5
N2 - 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.
AB - 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.
KW - Epigenetics
KW - High throughput screening
KW - Histone acetyltransferase
KW - Inhibitor
KW - MOF
UR - https://www.scopus.com/pages/publications/85051971406
U2 - 10.1016/j.ejmech.2018.08.026
DO - 10.1016/j.ejmech.2018.08.026
M3 - 文章
C2 - 30145373
AN - SCOPUS:85051971406
SN - 0223-5234
VL - 157
SP - 867
EP - 876
JO - European Journal of Medicinal Chemistry
JF - European Journal of Medicinal Chemistry
ER -