Abstract
Ca2+ influx via store-operated Ca2+ release activated Ca2+ (CRARAC) channels represents a main signaling pathway for T-cell activation as well as mast-cell degranulation. The ERER-located Ca 2+-sensor, STIM1 and the Ca2+-selective ion pore, Orai1 in the membrane are sufficient to fully reconstitute CRARAC currents. Their identification, but even more the recent structural resolution of both proteins by X-ray crystallography has substantially advanced the understanding of the activation mechanism of CRARAC channels. In this review, we provide a detailed description of the STIM1/Orai1 signaling pathway thereby focusing on the critical domains mediating both, intra - as well as intermolecular interactions and on the ion permeation pathway. Based on the results of functional studies as well as the recently published crystal structures, we portray a mechanistic view of the steps in the CRARAC channel signaling cascade ranging from STIM1 oligomerization over STIM1-Orai1 coupling to the ultimate Orai1 channel activation and permeation. © 2013 Landes Bioscience.
Author supplied keywords
Cite
CITATION STYLE
Fahrner, M., Derler, I., Jardin, I., & Romanin, C. (2013). The STIM1/Orai signaling machinery. Channels, 7(5), 330–343. https://doi.org/10.4161/chan.26742
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.