DANGER, a novel regulatory protein of inositol 1,4,5-trisphosphate-receptor activity

J Biol Chem. 2006 Dec 1;281(48):37111-6. doi: 10.1074/jbc.M608760200. Epub 2006 Sep 21.

Abstract

We report the cloning and characterization of DANGER, a novel protein which physiologically binds to inositol 1,4,5-trisphosphate receptors (IP(3)R). DANGER is a membrane-associated protein predicted to contain a partial MAB-21 domain. It is expressed in a wide variety of neuronal cell lineages where it localizes to membranes in the cell periphery together with IP(3)R. DANGER interacts with IP(3)R in vitro and co-immunoprecipitates with IP(3)R from cellular preparations. DANGER robustly enhances Ca(2+)-mediated inhibition of IP(3) RCa(2+) release without affecting IP(3) binding in microsomal assays and inhibits gating in single-channel recordings of IP(3)R. DANGER appears to allosterically modulate the sensitivity of IP(3) RtoCa(2+) inhibition, which likely alters IP(3)R-mediated Ca(2+) dynamics in cells where DANGER and IP(3)R are co-expressed.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Allosteric Site
  • Animals
  • Calcium / metabolism
  • Cloning, Molecular
  • Electrophysiology
  • Gene Expression Regulation*
  • Humans
  • Inositol 1,4,5-Trisphosphate Receptors / metabolism*
  • Insecta
  • Membrane Proteins / chemistry
  • Membrane Proteins / physiology*
  • Neurons / metabolism*
  • Protein Binding
  • Protein Structure, Tertiary
  • Rats
  • Trypsin / pharmacology
  • Two-Hybrid System Techniques

Substances

  • ITPRIP protein, human
  • Inositol 1,4,5-Trisphosphate Receptors
  • Membrane Proteins
  • Trypsin
  • Calcium