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Structural Characterization and Computer‐Aided Optimization of a Small‐Molecule Inhibitor of the Arp2/3 Complex, a Key Regulator of the Actin Cytoskeleton

2012; Wiley; Volume: 7; Issue: 7 Linguagem: Inglês

10.1002/cmdc.201200104

1860-7187

Andrew W. Baggett, Zoe Cournia, Min Suk Han, George Patargias, Adam Glass, Shih‐Yuan Liu, Brad J. Nolen,

RNA Research and Splicing

Abstract CK‐666 ( 1 ) is a recently discovered small‐molecule inhibitor of the actin‐related protein 2/3 (Arp2/3) complex, a key actin cytoskeleton regulator with roles in bacterial pathogenesis and cancer cell motility. Although 1 is commercially available, the crystal structure of Arp2/3 complex with 1 bound has not been reported, making its mechanism of action uncertain. Furthermore, its relatively low potency increases its potential for off‐target effects in vivo, complicating interpretation of its influence in cell biological studies and precluding its clinical use. Herein we report the crystal structure of 1 bound to Arp2/3 complex, which reveals that 1 binds between the Arp2 and Arp3 subunits to stabilize the inactive conformation of the complex. Based on the crystal structure, we used computational docking and free‐energy perturbation calculations of monosubstituted derivatives of 1 to guide optimization efforts. Biochemical assays of ten newly synthesized compounds led to the identification of compound 2 , which exhibits a threefold increase in inhibitory activity in vitro relative to 1 . In addition, our computational analyses unveiled a surface groove at the interface of the Arp2 and Arp3 subunits that can be exploited for additional structure‐based optimization.