| Literature DB >> 14685260 |
Nael Nadif Kasri1, Anthony M Holmes, Geert Bultynck, Jan B Parys, Martin D Bootman, Katja Rietdorf, Ludwig Missiaen, Fraser McDonald, Humbert De Smedt, Stuart J Conway, Andrew B Holmes, Michael J Berridge, H Llewelyn Roderick.
Abstract
Inositol 1,4,5-trisphosphate receptors (InsP(3)Rs) were recently demonstrated to be activated independently of InsP(3) by a family of calmodulin (CaM)-like neuronal Ca(2+)-binding proteins (CaBPs). We investigated the interaction of both naturally occurring long and short CaBP1 isoforms with InsP(3)Rs, and their functional effects on InsP(3)R-evoked Ca(2+) signals. Using several experimental paradigms, including transient expression in COS cells, acute injection of recombinant protein into Xenopus oocytes and (45)Ca(2+) flux from permeabilised COS cells, we demonstrated that CaBPs decrease the sensitivity of InsP(3)-induced Ca(2+) release (IICR). In addition, we found a Ca(2+)-independent interaction between CaBP1 and the NH(2)-terminal 159 amino acids of the type 1 InsP(3)R. This interaction resulted in decreased InsP(3) binding to the receptor reminiscent of that observed for CaM. Unlike CaM, however, CaBPs do not inhibit ryanodine receptors, have a higher affinity for InsP(3)Rs and more potently inhibited IICR. We also show that phosphorylation of CaBP1 at a casein kinase 2 consensus site regulates its inhibition of IICR. Our data suggest that CaBPs are endogenous regulators of InsP(3)Rs tuning the sensitivity of cells to InsP(3).Entities:
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Year: 2003 PMID: 14685260 PMCID: PMC1271747 DOI: 10.1038/sj.emboj.7600037
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598