Differential modulation of Ca2+/calmodulin-dependent protein kinase II activity by regulated interactions with N-methyl-D-aspartate receptor NR2B subunits and α-actinin

Abstract

Neuronal Ca2+/calmodulin-dependent protein kinase II (CaMKII) interacts with several prominent dendritic spine proteins, which have been termed CaMKII-associated proteins. The NR2B subunit of N-methyl-D-aspartate (NMDA)-type glutamate receptor, densin-180, and α-actinin bind comparable, approximately stoichiometric amounts of Thr286-autophosphorylated CaMKIIα, forming a ternary complex (Robison, A. J., Bass, M. A., Jiao, Y., Macmillan, L. B., Carmody, L. C., Bartlett, R. K., and Colbran, R. J. (2005) J. Biol. Chem. 280, 35329-35336), but their impacts on CaMKII function are poorly understood. Here we show that these interactions are differentially regulated and exert distinct effects on CaMKII activity. Nonphosphorylated and Thr 286-autophosphorylated CaMKII bind to α-actinin with similar efficacy, but autophosphorylation at Thr305/306 or Ca 2+/calmodulin binding significantly reduce this binding. Moreover, α-actinin antagonizes CaMKII activation by Ca2+/calmodulin, as assessed by autophosphorylation and phosphorylation of a peptide substrate. CaMKII binding to densin (1247-1542) is partially independent of Thr 286 autophosphorylation and is unaffected by Ca2+- independent autophosphorylation or Ca2+/calmodulin. In addition, the CaMKII binding domain of densin-180 has little effect on CaMKII activity. In contrast, the interaction of CaMKIIα with NR2B requires either Thr 286 autophosphorylation or the binding of both Ca2+/ calmodulin and adenine nucleotides. NR2B inhibits both the Ca 2+/calmodulin-dependent and autonomous activities of CaMKII by a mechanism that is competitive with autocamtide-2 substrate, non-competitive with syntide-2 substrate, and uncompetitive with respect to ATP. In combination, these data suggest that dynamically regulated interactions with CaMKII-associated proteins could play pleiotropic roles in fine-tuning CaMKII signaling in defined subcellular compartments. © 2005 by The American Society for Biochemistry and Molecular Biology, Inc.