Biochemistry · 2009 · 20 citations · 38 references
Life SciencesCell BiologyMolecular BiologyCytoskeletonDrug DiscoveryMolecular Cell BiologyCytoskeletal Associated ProteinsEnzyme InhibitionMicrotubule-associated ProteinsMitotic InhibitorsMitotic SpindleMotor ProteinsAnticancer ActivityInhibitor Binding AffinityKinesin InhibitorsKinesin MotorsKinesin-associated ProteinsKinesin-mediated MotilityMitotic Spindle InhibitorsMotor Protein Inhibitors
Kinesin-5 proteins are essential for formation of a bipolar mitotic spindle in most and, perhaps all, eukaryotic cells. Several Kinesin-5 proteins, notably the human version, HsEg5, are targets of a constantly expanding group of small-molecule inhibitors, which hold promise both as tools for probing mechanochemical transduction and as anticancer agents. Although most such compounds are selective for HsEg5 and closely related Kinesin-5 proteins, some, such as NSC 622124, exhibit activity against at least one kinesin from outside the Kinesin-5 family. Here we show NSC 622124, despite identification in a screen that yielded inhibitors now known to target the HsEg5 monastrol-binding site, does not compete with [(14)C]monastrol for binding to HsEg5 and is able to inhibit the basal and microtubule-stimulated ATPase activity of the monastrol-insensitive Kinesin-5, KLP61F. NSC 622124 competes with microtubules, but not ATP, for interaction with HsEg5 and disrupts the microtubule binding of HsEg5, KLP61F, and Kinesin-1. Proteolytic degradation of an HsEg5.NSC622124 complex revealed that segments of the alpha3 and alpha5 helices map to the inhibitor-binding site. Overall, our results demonstrate that NSC 622124 targets the conserved microtubule-binding site of kinesin proteins. Further, unlike compounds previously reported to target the kinesin microtubule-binding site, NSC 622124 does not produce any enhancement of basal ATPase activity and thus acts solely as a negative regulator through interaction with a site traditionally viewed as a binding region for positive regulators (i.e., microtubules). Our work emphasizes the concept that microtubule-dependent motor proteins may be controlled at multiple sites by both positive and negative effectors.
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Microtubule Interaction Site of the Kinesin Motor
Günther Woehlke, Aaron Ruby, Cynthia L. Hart et al. · Cell · 1997 · 393 citations · Full text
Antitumor Activity of a Kinesin Inhibitor
Roman Sakowicz, Jeffrey T. Finer, Christophe Béraud et al. · Cancer Research · 2004 · 241 citations