Structure-based discovery of the first allosteric inhibitors of cyclin-dependent kinase 2
| Autor: | Andrew Anighoro, Laura Carrassa, Martina Chripkova, Giulio Rastelli, Massimo Broggini |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2014 |
| Předmět: |
Stereochemistry
Allosteric regulation Antineoplastic Agents Breast Neoplasms Ligands Retinoblastoma Protein Protein Structure Secondary Inhibitory Concentration 50 Structure-Activity Relationship Allosteric Regulation Cell Line Tumor Report Drug Discovery medicine Humans Staurosporine Molecular Targeted Therapy Phosphorylation Protein kinase A Protein Kinase Inhibitors Molecular Biology BEAR Cyclin-dependent kinase 2 allosteric inhibitors protein kinase structure-based drug design virtual screening Cell Proliferation Virtual screening Dose-Response Relationship Drug biology Drug discovery Kinase Cyclin-Dependent Kinase 2 Cell Biology Molecular Docking Simulation Biochemistry Docking (molecular) biology.protein Computer-Aided Design Female Protein Binding Signal Transduction Developmental Biology medicine.drug |
| Popis: | Allosteric targeting of protein kinases via displacement of the structural αC helix with type III allosteric inhibitors is currently gaining a foothold in drug discovery. Recently, the first crystal structure of CDK2 with an open allosteric pocket adjacent to the αC helix has been described, prospecting new opportunities to design more selective inhibitors, but the structure has not yet been exploited for the structure-based design of type III allosteric inhibitors. In this work we report the results of a virtual screening campaign that resulted in the discovery of the first-in-class type III allosteric ligands of CDK2. Using a combination of docking and post-docking analyses made with our tool BEAR, 7 allosteric ligands (hit rate of 20%) with micromolar affinity for CDK2 were identified, some of them inhibiting the growth of breast cancer cell lines in the micromolar range. Competition experiments performed in the presence of the ATP-competitive inhibitor staurosporine confirmed that the 7 ligands are truly allosteric, in agreement with their design. Of these, compound 2 bound CDK2 with an EC50 value of 3 μM and inhibited the proliferation of MDA-MB231 and ZR-75–1 breast cancer cells with IC50 values of approximately 20 μM, while compound 4 had an EC50 value of 71 μM and IC50 values around 4 μM. Remarkably, the most potent compound 4 was able to selectively inhibit CDK2-mediated Retinoblastoma phosphorylation, confirming that its mechanism of action is fully compatible with a selective inhibition of CDK2 phosphorylation in cells. Finally, hit expansion through analog search of the most potent inhibitor 4 revealed an additional ligand 4g with similar in vitro potency on breast cancer cells. |
| Databáze: | OpenAIRE |
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