Structure, Regulation and Biophysics of I(CRAC), STIM/Orai1

Research output: Contribution to journalArticlepeer-review

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.
Original languageEnglish
Pages (from-to)383-410
Number of pages28
JournalAdvances in Experimental Medicine and Biology
Issue number740
DOIs
Publication statusPublished - 2012

Fields of science

  • 103036 Theoretical physics
  • 211904 Biomechanics
  • 103020 Surface physics
  • 210 Nanotechnology
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  • 208 Environmental Biotechnology
  • 104014 Surface chemistry
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JKU Focus areas

  • Engineering and Natural Sciences (in general)

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