Projects per year
Abstract
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.
Original language | English |
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Pages (from-to) | 17677-17680 |
Number of pages | 4 |
Journal | Chemistry - A European Journal |
Volume | 24 |
Issue number | 67 |
Early online date | 12 Sep 2018 |
DOIs | |
Publication status | Published - 3 Dec 2018 |
Keywords
- HECT Ubiquitin Ligase
- saturation transfer difference NMR
- DEEP-STD NMR
Profiles
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Jesus Angulo
- School of Chemistry, Pharmacy and Pharmacology - Honorary Senior Lecturer
- Pharmaceutical Materials and Soft Matter - Member
Person: Honorary, Research Group Member
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Andrew Hemmings
- School of Biological Sciences - Professor of Structural Biology
- School of Chemistry, Pharmacy and Pharmacology - Professor
- Centre for Molecular and Structural Biochemistry - Member
- Chemistry of Life Processes - Member
- Molecular Microbiology - Member
- Plant Sciences - Member
Person: Research Group Member, Research Centre Member, Academic, Teaching & Research
Projects
- 1 Finished
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Targeting WW domain function in ubiquitin overexpressed in prostate cancer
Chantry, A., Blumenschein, T. & Cooper, C.
1/10/14 → 30/09/17
Project: Research