Exploiting Protein Conformational Change to Optimize Adenosine-Derived Inhibitors of HSP70.
van Montfort, RL
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HSP70 is a molecular chaperone and a key component of the heat-shock response. Because of its proposed importance in oncology, this protein has become a popular target for drug discovery, efforts which have as yet brought little success. This study demonstrates that adenosine-derived HSP70 inhibitors potentially bind to the protein with a novel mechanism of action, the stabilization by desolvation of an intramolecular salt-bridge which induces a conformational change in the protein, leading to high affinity ligands. We also demonstrate that through the application of this mechanism, adenosine-derived HSP70 inhibitors can be optimized in a rational manner.
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Medicinal Chemistry 2
Medicinal Chemistry 3
Hit Discovery & Structural Design
Structure-Based Drug Design
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Journal of medicinal chemistry, 2016, 59 (10), pp. 4625 - 4636