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Ca(2+) release-activated Ca(2+) (CRAC) current, structure, and function

Store-operated Ca(2+) entry describes the phenomenon that connects a depletion of internal Ca(2+) stores to an activation of plasma membrane-located Ca(2+) selective ion channels. Tremendous progress towards the underlying molecular mechanism came with the discovery of the two respective limiting co...

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Detalles Bibliográficos
Autores principales: Muik, Martin, Schindl, Rainer, Fahrner, Marc, Romanin, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SP Birkhäuser Verlag Basel 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3505497/
https://www.ncbi.nlm.nih.gov/pubmed/22802126
http://dx.doi.org/10.1007/s00018-012-1072-8
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author Muik, Martin
Schindl, Rainer
Fahrner, Marc
Romanin, Christoph
author_facet Muik, Martin
Schindl, Rainer
Fahrner, Marc
Romanin, Christoph
author_sort Muik, Martin
collection PubMed
description Store-operated Ca(2+) entry describes the phenomenon that connects a depletion of internal Ca(2+) stores to an activation of plasma membrane-located Ca(2+) selective ion channels. Tremendous progress towards the underlying molecular mechanism came with the discovery of the two respective limiting components, STIM and Orai. STIM1 represents the ER-located Ca(2+) sensor and transmits the signal of store depletion to the plasma membrane. Here it couples to and activates Orai, the highly Ca(2+)-selective pore-forming subunit of Ca(2+) release-activated Ca(2+) channels. In this review, we focus on the molecular steps that these two proteins undergo from store-depletion to their coupling, the activation, and regulation of Ca(2+) currents.
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spelling pubmed-35054972012-11-28 Ca(2+) release-activated Ca(2+) (CRAC) current, structure, and function Muik, Martin Schindl, Rainer Fahrner, Marc Romanin, Christoph Cell Mol Life Sci Review Store-operated Ca(2+) entry describes the phenomenon that connects a depletion of internal Ca(2+) stores to an activation of plasma membrane-located Ca(2+) selective ion channels. Tremendous progress towards the underlying molecular mechanism came with the discovery of the two respective limiting components, STIM and Orai. STIM1 represents the ER-located Ca(2+) sensor and transmits the signal of store depletion to the plasma membrane. Here it couples to and activates Orai, the highly Ca(2+)-selective pore-forming subunit of Ca(2+) release-activated Ca(2+) channels. In this review, we focus on the molecular steps that these two proteins undergo from store-depletion to their coupling, the activation, and regulation of Ca(2+) currents. SP Birkhäuser Verlag Basel 2012-07-17 2012 /pmc/articles/PMC3505497/ /pubmed/22802126 http://dx.doi.org/10.1007/s00018-012-1072-8 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Review
Muik, Martin
Schindl, Rainer
Fahrner, Marc
Romanin, Christoph
Ca(2+) release-activated Ca(2+) (CRAC) current, structure, and function
title Ca(2+) release-activated Ca(2+) (CRAC) current, structure, and function
title_full Ca(2+) release-activated Ca(2+) (CRAC) current, structure, and function
title_fullStr Ca(2+) release-activated Ca(2+) (CRAC) current, structure, and function
title_full_unstemmed Ca(2+) release-activated Ca(2+) (CRAC) current, structure, and function
title_short Ca(2+) release-activated Ca(2+) (CRAC) current, structure, and function
title_sort ca(2+) release-activated ca(2+) (crac) current, structure, and function
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3505497/
https://www.ncbi.nlm.nih.gov/pubmed/22802126
http://dx.doi.org/10.1007/s00018-012-1072-8
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