Discovery of Small Molecule WWP2 Ubiquitin Ligase Inhibitors

被引:28
|
作者
Watt, Jessica E. [1 ]
Hughes, Gregory R. [1 ,3 ]
Walpole, Samuel [2 ]
Monaco, Serena [2 ]
Stephenson, G. Richard [3 ]
Page, Philip C. Bulman [3 ]
Hemmings, Andrew M. [1 ,3 ]
Angulo, Jesus [2 ]
Chantry, Andrew [1 ]
机构
[1] Univ East Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England
[2] Univ East Anglia, Sch Pharm, Norwich NR4 7TJ, Norfolk, England
[3] Univ East Anglia, Sch Chem, Norwich NR4 7TJ, Norfolk, England
基金
英国生物技术与生命科学研究理事会;
关键词
DEEP-STD NMR; drug discovery; ubiquitin ligase; inhibitors; saturation transfer difference NMR; NMR; ISOFORMS; INDOLE-3-CARBINOL; NEDD4-1; DOMAIN;
D O I
10.1002/chem.201804169
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have screened small molecule libraries specifically for inhibitors that target WWP2, an E3 ubiquitin ligase associated with tumour outgrowth and spread. Selected hits demonstrated dose-dependent WWP2 inhibition, low micromolar IC50 values, and inhibition of PTEN substrate-specific ubiquitination. Binding to WWP2 was confirmed by ligand-based NMR spectroscopy. Furthermore, we used a combination of STD NMR, the recently developed DEEP-STD NMR approach, and docking calculations, to propose for the first time an NMR-validated 3D molecular model of a WWP2-inhibitor complex. These first generation WWP2 inhibitors provide a molecular framework for informing organic synthetic approaches to improve activity and selectivity.
引用
收藏
页码:17677 / 17680
页数:4
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