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J. Biol. Chem. 278 (50): 49667-49670

© 2003 by The American Society for Biochemistry and Molecular Biology, Inc.

A New Role for IQ Motif Proteins in Regulating Calmodulin Function*Formula

John A. Putkey{ddagger}§, Quinn Kleerekoper{ddagger}, Tara R. Gaertner, , and M. Neal Waxham

Departments of Biochemistry and Molecular Biology, and Neurobiology and Anatomy, University of Texas Medical School, Houston, Texas 77030

Abstract: IQ motifs are found in diverse families of calmodulin (CaM)-binding proteins. Some of these, like PEP-19 and RC3, are highly abundant in neuronal tissues, but being devoid of catalytic activity, their biological roles are not understood. We hypothesized that these IQ motif proteins might have unique effects on the Ca2+ binding properties of CaM, since they bind to CaM in the presence or absence of Ca2+. Here we show that PEP-19 accelerates by 40 to 50-fold both the slow association and dissociation of Ca2+ from the C-domain of free CaM, and we identify the sites of interaction between CaM and PEP-19 using NMR. Importantly, we demonstrate that PEP-19 can also increase the rate of dissociation of Ca2+ from CaM when bound to intact CaM-dependent protein kinase II. Thus, PEP-19, and presumably similar members of the IQ family of proteins, has the potential to alter the Ca2+-binding dynamics of free CaM and CaM that is bound to other target proteins. Since Ca2+ binding to the C-domain of CaM is the rate-limiting step for activation of CaM-dependent enzymes, the data reveal a new concept of importance in understanding the temporal dynamics of Ca2+-dependent cell signaling.

Received for publication August 21, 2003. Revision received September 22, 2003.

§ To whom correspondence should be addressed: Depts. of Biochemistry and Molecular Biology, University of Texas Medical School, 6431 Fannin, Houston, TX 77030. Tel.: 713-500-6061; Fax: 713-500-0652; E-mail: John.Putkey{at}

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