Dynamic Response of the C2 Domain of Protein Kinase Cα to Ca²⁺ Binding.

ABSTRACT: Ca²⁺-dependent conserved-region 2 (C2) domains target their host signaling proteins to anionic membranes. The Ca²⁺-binding event is a prerequisite for membrane association. Here, we investigate multiscale metal-ion-dependent dynamics of the C2 domain of protein kinase Cα (C2α) using NMR spectroscopy. Interactions with metal ions attenuate microsecond-timescale motions of the loop regions, indicating that preorganization of the metal-binding loops occurs before membrane insertion. Binding of a full complement of Ca²⁺ ions has a profound effect on the millisecond-timescale dynamics of the N- and C-terminal regions of C2α. We propose that Ca²⁺ binding allosterically destabilizes the terminal regions of C2α and thereby facilitates the conformational

SUBMITTER: Morales KA 

PROVIDER: S-EPMC5071625 | biostudies-literature | 2016 Oct

REPOSITORIES: biostudies-literature