Recent progress on STIM1 domains controlling Orai activation

• Published in: Cell calcium (Edinburgh) Vol. 46; no. 4; pp. 227 - 232
• Main Authors: Schindl, R, Muik, M, Fahrner, M, Derler, I, Fritsch, R, Bergsmann, J, Romanin, C
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier India Pvt Ltd 01.10.2009
• Subjects: Advanced Basic Science; Animals; Calcium - chemistry; Calcium - metabolism; Calcium Channels - chemistry; Calcium Channels - metabolism; Calcium Channels - ultrastructure; Cell Membrane - metabolism; Cell Membrane - ultrastructure; CRAC; Endoplasmic Reticulum - metabolism; Endoplasmic Reticulum - ultrastructure; Fast inactivation; Humans; Ion Channel Gating; Membrane Proteins - chemistry; Membrane Proteins - metabolism; Membrane Proteins - ultrastructure; Neoplasm Proteins - chemistry; Neoplasm Proteins - metabolism; Neoplasm Proteins - ultrastructure; Orai; ORAI1 Protein; Protein Binding; Protein Interaction Domains and Motifs; STIM1; STIM1–Orai coupling; Stromal Interaction Molecule 1; STIM1–Orai coupling; Fast inactivation; STIM1; Orai; CRAC
• ISSN: 0143-4160; 1532-1991
• DOI: 10.1016/j.ceca.2009.08.003

Abstract Ca2+ entry in non-excitable cells is mainly carried by store-operated channels among which the CRAC channel is best characterized. Its two limiting molecular components are represented by the Ca2+ sensor protein STIM1 located in the endoplasmic reticulum and Orai1 in the plasma membrane. STIM1 senses a decrease of the Ca2+ content in internal stores and triggers its accumulation into puncta like structures resulting in coupling to as well as activation of Orai1 channels. The STIM1–Orai coupling process is determined by an interaction via their C-termini. This review highlights recent developments on domains particularly within the cytosolic part of STIM1 that govern this interaction.