-
Something wrong with this record ?
CRAC channel opening is determined by a series of Orai1 gating checkpoints in the transmembrane and cytosolic regions
A. Tiffner, R. Schober, C. Höglinger, D. Bonhenry, S. Pandey, V. Lunz, M. Sallinger, I. Frischauf, M. Fahrner, S. Lindinger, L. Maltan, S. Berlansky, M. Stadlbauer, R. Schindl, R. Ettrich, C. Romanin, I. Derler
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
P 27641
Austrian Science Fund FWF - Austria
P 28701
Austrian Science Fund FWF - Austria
NLK
Directory of Open Access Journals
from 2021
Free Medical Journals
from 2008 to 1 year ago
Freely Accessible Science Journals
from 1905 to 1 year ago
PubMed Central
from 2005
Europe PubMed Central
from 2005 to 1 year ago
Open Access Digital Library
from 1905-10-01
Open Access Digital Library
from 1905-10-01
ROAD: Directory of Open Access Scholarly Resources
from 1905
- MeSH
- Bacterial Proteins genetics metabolism MeSH
- Phosphatidylcholines chemistry metabolism MeSH
- Ion Channel Gating genetics MeSH
- Genetic Vectors chemistry metabolism MeSH
- HEK293 Cells MeSH
- Protein Interaction Domains and Motifs MeSH
- Protein Conformation, alpha-Helical MeSH
- Protein Conformation, beta-Strand MeSH
- Humans MeSH
- Liposomes chemistry metabolism MeSH
- Luminescent Proteins genetics metabolism MeSH
- Patch-Clamp Techniques MeSH
- Mutation MeSH
- Neoplasm Proteins chemistry genetics metabolism MeSH
- ORAI1 Protein chemistry genetics metabolism MeSH
- Stromal Interaction Molecule 1 chemistry genetics metabolism MeSH
- Gene Expression Regulation MeSH
- Recombinant Proteins chemistry genetics metabolism MeSH
- Genes, Reporter MeSH
- Molecular Dynamics Simulation MeSH
- Amino Acid Substitution MeSH
- Calcium metabolism MeSH
- Calcium Signaling * MeSH
- Protein Binding MeSH
- Binding Sites MeSH
- Green Fluorescent Proteins genetics metabolism MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
The initial activation step in the gating of ubiquitously expressed Orai1 calcium (Ca2+) ion channels represents the activation of the Ca2+-sensor protein STIM1 upon Ca2+ store depletion of the endoplasmic reticulum. Previous studies using constitutively active Orai1 mutants gave rise to, but did not directly test, the hypothesis that STIM1-mediated Orai1 pore opening is accompanied by a global conformational change of all Orai transmembrane domain (TM) helices within the channel complex. We prove that a local conformational change spreads omnidirectionally within the Orai1 complex. Our results demonstrate that these locally induced global, opening-permissive TM motions are indispensable for pore opening and require clearance of a series of Orai1 gating checkpoints. We discovered these gating checkpoints in the middle and cytosolic extended TM domain regions. Our findings are based on a library of double point mutants that contain each one loss-of-function with one gain-of-function point mutation in a series of possible combinations. We demonstrated that an array of loss-of-function mutations are dominant over most gain-of-function mutations within the same as well as of an adjacent Orai subunit. We further identified inter- and intramolecular salt-bridge interactions of Orai subunits as a core element of an opening-permissive Orai channel architecture. Collectively, clearance and synergistic action of all these gating checkpoints are required to allow STIM1 coupling and Orai1 pore opening. Our results unravel novel insights in the preconditions of the unique fingerprint of CRAC channel activation, provide a valuable source for future structural resolutions, and help to understand the molecular basis of disease-causing mutations.
College of Biomedical Sciences Larkin University Miami Florida USA
Faculty of Mathematics and Physics Charles University Prague Czechia
Gottfried Schatz Research Center Medical University of Graz Graz Austria
Institute of Biophysics JKU Life Science Center Johannes Kepler University Linz Linz Austria
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21026264
- 003
- CZ-PrNML
- 005
- 20211026133041.0
- 007
- ta
- 008
- 211013s2021 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1074/jbc.RA120.015548 $2 doi
- 035 __
- $a (PubMed)33361160
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Tiffner, Adéla $u Institute of Biophysics, JKU Life Science Center, Johannes Kepler University Linz, Linz, Austria
- 245 10
- $a CRAC channel opening is determined by a series of Orai1 gating checkpoints in the transmembrane and cytosolic regions / $c A. Tiffner, R. Schober, C. Höglinger, D. Bonhenry, S. Pandey, V. Lunz, M. Sallinger, I. Frischauf, M. Fahrner, S. Lindinger, L. Maltan, S. Berlansky, M. Stadlbauer, R. Schindl, R. Ettrich, C. Romanin, I. Derler
- 520 9_
- $a The initial activation step in the gating of ubiquitously expressed Orai1 calcium (Ca2+) ion channels represents the activation of the Ca2+-sensor protein STIM1 upon Ca2+ store depletion of the endoplasmic reticulum. Previous studies using constitutively active Orai1 mutants gave rise to, but did not directly test, the hypothesis that STIM1-mediated Orai1 pore opening is accompanied by a global conformational change of all Orai transmembrane domain (TM) helices within the channel complex. We prove that a local conformational change spreads omnidirectionally within the Orai1 complex. Our results demonstrate that these locally induced global, opening-permissive TM motions are indispensable for pore opening and require clearance of a series of Orai1 gating checkpoints. We discovered these gating checkpoints in the middle and cytosolic extended TM domain regions. Our findings are based on a library of double point mutants that contain each one loss-of-function with one gain-of-function point mutation in a series of possible combinations. We demonstrated that an array of loss-of-function mutations are dominant over most gain-of-function mutations within the same as well as of an adjacent Orai subunit. We further identified inter- and intramolecular salt-bridge interactions of Orai subunits as a core element of an opening-permissive Orai channel architecture. Collectively, clearance and synergistic action of all these gating checkpoints are required to allow STIM1 coupling and Orai1 pore opening. Our results unravel novel insights in the preconditions of the unique fingerprint of CRAC channel activation, provide a valuable source for future structural resolutions, and help to understand the molecular basis of disease-causing mutations.
- 650 _2
- $a substituce aminokyselin $7 D019943
- 650 _2
- $a bakteriální proteiny $x genetika $x metabolismus $7 D001426
- 650 _2
- $a vazebná místa $7 D001665
- 650 _2
- $a vápník $x metabolismus $7 D002118
- 650 12
- $a vápníková signalizace $7 D020013
- 650 _2
- $a regulace genové exprese $7 D005786
- 650 _2
- $a reportérové geny $7 D017930
- 650 _2
- $a genetické vektory $x chemie $x metabolismus $7 D005822
- 650 _2
- $a zelené fluorescenční proteiny $x genetika $x metabolismus $7 D049452
- 650 _2
- $a HEK293 buňky $7 D057809
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a gating iontového kanálu $x genetika $7 D015640
- 650 _2
- $a liposomy $x chemie $x metabolismus $7 D008081
- 650 _2
- $a luminescentní proteiny $x genetika $x metabolismus $7 D008164
- 650 _2
- $a simulace molekulární dynamiky $7 D056004
- 650 _2
- $a mutace $7 D009154
- 650 _2
- $a nádorové proteiny $x chemie $x genetika $x metabolismus $7 D009363
- 650 _2
- $a protein ORAI1 $x chemie $x genetika $x metabolismus $7 D000071740
- 650 _2
- $a metoda terčíkového zámku $7 D018408
- 650 _2
- $a fosfatidylcholiny $x chemie $x metabolismus $7 D010713
- 650 _2
- $a vazba proteinů $7 D011485
- 650 _2
- $a konformace proteinů, alfa-helix $7 D000072756
- 650 _2
- $a konformace proteinů, beta-řetězec $7 D000072757
- 650 _2
- $a interakční proteinové domény a motivy $7 D054730
- 650 _2
- $a rekombinantní proteiny $x chemie $x genetika $x metabolismus $7 D011994
- 650 _2
- $a protein STIM1 $x chemie $x genetika $x metabolismus $7 D000071737
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Schober, Romana $u Institute of Biophysics, JKU Life Science Center, Johannes Kepler University Linz, Linz, Austria
- 700 1_
- $a Höglinger, Carmen $u Institute of Biophysics, JKU Life Science Center, Johannes Kepler University Linz, Linz, Austria
- 700 1_
- $a Bonhenry, Daniel $u Center for Nanobiology and Structural Biology, Institute of Microbiology, Czech Academy of Sciences, Nove Hrady, Czechia
- 700 1_
- $a Pandey, Saurabh $u Center for Nanobiology and Structural Biology, Institute of Microbiology, Czech Academy of Sciences, Nove Hrady, Czechia
- 700 1_
- $a Lunz, Victoria $u Institute of Biophysics, JKU Life Science Center, Johannes Kepler University Linz, Linz, Austria
- 700 1_
- $a Sallinger, Matthias $u Institute of Biophysics, JKU Life Science Center, Johannes Kepler University Linz, Linz, Austria
- 700 1_
- $a Frischauf, Irene $u Institute of Biophysics, JKU Life Science Center, Johannes Kepler University Linz, Linz, Austria
- 700 1_
- $a Fahrner, Marc $u Institute of Biophysics, JKU Life Science Center, Johannes Kepler University Linz, Linz, Austria
- 700 1_
- $a Lindinger, Sonja $u Institute of Biophysics, JKU Life Science Center, Johannes Kepler University Linz, Linz, Austria
- 700 1_
- $a Maltan, Lena $u Institute of Biophysics, JKU Life Science Center, Johannes Kepler University Linz, Linz, Austria
- 700 1_
- $a Berlansky, Sascha $u Institute of Biophysics, JKU Life Science Center, Johannes Kepler University Linz, Linz, Austria
- 700 1_
- $a Stadlbauer, Michael $u Institute of Biophysics, JKU Life Science Center, Johannes Kepler University Linz, Linz, Austria
- 700 1_
- $a Schindl, Rainer $u Gottfried Schatz Research Center, Medical University of Graz, Graz, Austria
- 700 1_
- $a Ettrich, Rudiger $u College of Biomedical Sciences, Larkin University, Miami, Florida, USA; Faculty of Mathematics and Physics, Charles University, Prague, Czechia; Department of Cellular Biology & Pharmacology, Herbert Wertheim College of Medicine, Florida International University, Miami, Florida, USA
- 700 1_
- $a Romanin, Christoph $u Institute of Biophysics, JKU Life Science Center, Johannes Kepler University Linz, Linz, Austria
- 700 1_
- $a Derler, Isabella $u Institute of Biophysics, JKU Life Science Center, Johannes Kepler University Linz, Linz, Austria. Electronic address: Isabella.derler@jku.at
- 773 0_
- $w MED00002546 $t The Journal of biological chemistry $x 1083-351X $g Roč. 296, č. - (2021), s. 100224
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/33361160 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20211013 $b ABA008
- 991 __
- $a 20211026133047 $b ABA008
- 999 __
- $a ok $b bmc $g 1715088 $s 1146771
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2021 $b 296 $c - $d 100224 $e 20201229 $i 1083-351X $m The Journal of biological chemistry $n J Biol Chem $x MED00002546
- GRA __
- $a P 27641 $p Austrian Science Fund FWF $2 Austria
- GRA __
- $a P 28701 $p Austrian Science Fund FWF $2 Austria
- LZP __
- $a Pubmed-20211013