Structure, regulation and biophysics of I(CRAC), STIM/Orai1

Adv Exp Med Biol. 2012:740:383-410. doi: 10.1007/978-94-007-2888-2_16.

Abstract

Ca(2+) release activated Ca(2+) (CRAC) channels mediate robust Ca(2+) influx when the endoplasmic reticulum Ca(2+) stores are depleted. This essential process for T-cell activation as well as degranulation of mast cells involves the Ca(2+) sensor STIM1, located in the endoplasmic reticulum and the Ca(2+) selective Orai1 channel in the plasma membrane. Our review describes the CRAC signaling pathway, the activation of which is initiated by a drop in the endoplasmic Ca(2+) level sensed by STIM1. This in term induces multimerisation and puncta-formation of STIM1 proteins is followed by their coupling to and activation of Orai channels. Consequently Ca(2+) entry is triggered through the Orai pore into the cytosol with subsequent closure of the channel by Ca(2+)-dependent inactivation. We will portray a mechanistic view of the events coupling STIM1 to Orai activation based on their structure and biophysics.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Boron Compounds / pharmacology
  • Calcium Channels / chemistry
  • Calcium Channels / physiology*
  • Humans
  • Membrane Proteins / chemistry
  • Membrane Proteins / physiology*
  • Neoplasm Proteins / chemistry
  • Neoplasm Proteins / physiology*
  • ORAI1 Protein
  • Oxidative Stress
  • Protein Multimerization
  • Signal Transduction
  • Stromal Interaction Molecule 1

Substances

  • Boron Compounds
  • Calcium Channels
  • Membrane Proteins
  • Neoplasm Proteins
  • ORAI1 Protein
  • ORAI1 protein, human
  • STIM1 protein, human
  • Stromal Interaction Molecule 1
  • 2-aminoethoxydiphenyl borate