Coiled-Coil Formation Conveys a STIM1 Signal from ER Lumen to Cytoplasm

Publication date: 2 January 2018
Source:Cell Reports, Volume 22, Issue 1
Author(s): Nupura Hirve, Vangipurapu Rajanikanth, Patrick G. Hogan, Aparna Gudlur
STIM1 and STIM2 are endoplasmic reticulum (ER) membrane proteins that sense decreases in ER-luminal free Ca²⁺ and, through a conformational change in the STIM cytoplasmic domain, control gating of the plasma membrane Ca²⁺ channel ORAI1. To determine how STIM1 conveys a signal from the ER lumen to the cytoplasm, we studied the Ca²⁺-dependent conformational change of engineered STIM1 proteins in isolated ER membranes and, in parallel, physiological activation of these proteins in cells. We find that conserved "sentinel" features of the CC1 region help to prevent activation while Ca²⁺ is bound to STIM ER-luminal domains. Reduced ER-luminal Ca²⁺ drives a concerted conformational change, in which STIM luminal domains rearrange and the STIM transmembrane helices and initial parts of the CC1 regions pair in an extended coiled coil. This intradimer rearrangement overcomes the relatively weak CC1-SOAR/CAD interactions that hold STIM in an inactive conformation, releasing the SOAR/CAD domain to activate ORAI channels.

Graphical abstract

Teaser

STIM1 and STIM2 play a central role in cellular Ca²⁺ balance and Ca²⁺ signaling by monitoring free Ca²⁺ in the endoplasmic reticulum and communicating this information to plasma membrane Ca²⁺ channels. Hirve et al. dissect the structural change that transmits the signal from the STIM1 ER-luminal domain to the STIM1 cytoplasmic domain.


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