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Ca(2+)-dependent Binding and Activation of Dormant Ezrin by Dimeric S100P

By Max Koltzscher, Claudia Neumann, Simone König and Volker Gerke


S100 proteins are EF hand type Ca(2)(+) binding proteins thought to function in stimulus-response coupling by binding to and thereby regulating cellular targets in a Ca(2)(+)-dependent manner. To isolate such target(s) of the S100P protein we devised an affinity chromatography approach that selects for S100 protein ligands requiring the biologically active S100 dimer for interaction. Hereby we identify ezrin, a membrane/F-actin cross-linking protein, as a dimer-specific S100P ligand. S100P-ezrin complex formation is Ca(2)(+) dependent and most likely occurs within cells because both proteins colocalize at the plasma membrane after growth factor or Ca(2)(+) ionophore stimulation. The S100P binding site is located in the N-terminal domain of ezrin and is accessible for interaction in dormant ezrin, in which binding sites for F-actin and transmembrane proteins are masked through an association between the N- and C-terminal domains. Interestingly, S100P binding unmasks the F-actin binding site, thereby at least partially activating the ezrin molecule. This identifies S100P as a novel activator of ezrin and indicates that activation of ezrin's cross-linking function can occur directly in response to Ca(2)(+) transients

Topics: Articles
Publisher: The American Society for Cell Biology
Year: 2003
DOI identifier: 10.1091/mbc.E02-09-0553
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Provided by: PubMed Central
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