Calmodulin regulates Ca2+-sensing receptor-mediated Ca2+ signaling and its cell surface expression.
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The Ca(2+)-sensing receptor (CaSR) is a member of family C of the GPCRs responsible for sensing extracellular Ca(2+) ([Ca(2+)](o)) levels, maintaining extracellular Ca(2+) homeostasis, and transducing Ca(2+) signaling from the extracellular milieu to the intracellular environment. In the present study, we have demonstrated a Ca(2+)-dependent, stoichiometric interaction between CaM and a CaM-binding domain (CaMBD) located within the C terminus of CaSR (residues 871-898). Our studies suggest a wrapping around 1-14-like mode of interaction that involves global conformational changes in both lobes of CaM with concomitant formation of a helical structure in the CaMBD. More importantly, the Ca(2+)-dependent association between CaM and the C terminus of CaSR is critical for maintaining proper responsiveness of intracellular Ca(2+) responses to changes in extracellular Ca(2+) and regulating cell surface expression of the receptor.
author list (cited authors)
Huang, Y., Zhou, Y., Wong, H., Castiblanco, A., Chen, Y., Brown, E. M., & Yang, J. J.
complete list of authors
Huang, Yun||Zhou, Yubin||Wong, Hing-Cheung||Castiblanco, Adriana||Chen, Yanyi||Brown, Edward M||Yang, Jenny J