Original Articles: 2010 Vol: 2 Issue: 5
RSK2 Binding Models Delineate Key Features for Activity
Abstract
Due to its overexpression and activation in human cancer cells and tissues, an emerging molecular target
in cancer therapeutics is p90 ribosomal s6 kinase 2 (RSK2). While a growing number of RSK2 inhibitors
have been reported in the literature, only the crystal structure of RSK2 in complex with an AMP analogue
provides a structural basis for understanding RSK2 inhibition. To remedy this, we used our fluorescence
polarization assay to determine the RSK2 activity for a set of structurally diverse compounds, and
followed this by modeling their binding modes in an all-atom, energy refined crystal structure of RSK2.
These binding models reveal that Val131 and Leu147 are key interaction sites for potent RSK2 inhibition.
This structure-based pharmacophore is an important tool for new lead discovery and refinement.