A dual mechanism promotes switching of the Stormorken STIM1 R304W mutant into the activated state
Language English Country England, Great Britain Media electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
P 27263
Austrian Science Fund FWF - Austria
P 28123
Austrian Science Fund FWF - Austria
P 28498
Austrian Science Fund FWF - Austria
PubMed
29483506
PubMed Central
PMC5827659
DOI
10.1038/s41467-018-03062-w
PII: 10.1038/s41467-018-03062-w
Knihovny.cz E-resources
- MeSH
- Erythrocytes, Abnormal metabolism pathology MeSH
- Bacterial Proteins genetics metabolism MeSH
- Point Mutation * MeSH
- Dyslexia genetics metabolism pathology MeSH
- Gene Expression MeSH
- HEK293 Cells MeSH
- Ichthyosis genetics metabolism pathology MeSH
- Protein Interaction Domains and Motifs MeSH
- Ion Transport MeSH
- Protein Conformation, alpha-Helical MeSH
- Humans MeSH
- Luminescent Proteins genetics metabolism MeSH
- Patch-Clamp Techniques MeSH
- Migraine Disorders genetics metabolism pathology MeSH
- Miosis genetics metabolism pathology MeSH
- Models, Molecular MeSH
- Protein Multimerization 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
- Amino Acid Sequence MeSH
- Spleen abnormalities metabolism pathology MeSH
- Amino Acid Substitution MeSH
- Muscle Fatigue genetics MeSH
- Blood Platelet Disorders genetics metabolism pathology MeSH
- Calcium chemistry metabolism 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
- Names of Substances
- Bacterial Proteins MeSH
- Cyan Fluorescent Protein MeSH Browser
- Luminescent Proteins MeSH
- Neoplasm Proteins MeSH
- ORAI1 protein, human MeSH Browser
- ORAI1 Protein MeSH
- Stromal Interaction Molecule 1 MeSH
- Recombinant Proteins MeSH
- STIM1 protein, human MeSH Browser
- Calcium MeSH
- yellow fluorescent protein, Bacteria MeSH Browser
- Green Fluorescent Proteins MeSH
STIM1 and Orai1 are key components of the Ca2+-release activated Ca2+ (CRAC) current. Orai1, which represents the subunit forming the CRAC channel complex, is activated by the ER resident Ca2+ sensor STIM1. The genetically inherited Stormorken syndrome disease has been associated with the STIM1 single point R304W mutant. The resulting constitutive activation of Orai1 mainly involves the CRAC-activating domain CAD/SOAR of STIM1, the exposure of which is regulated by the molecular interplay between three cytosolic STIM1 coiled-coil (CC) domains. Here we present a dual mechanism by which STIM1 R304W attains the pathophysiological, constitutive activity eliciting the Stormorken syndrome. The R304W mutation induces a helical elongation within the CC1 domain, which together with an increased CC1 homomerization, destabilize the resting state of STIM1. This culminates, even in the absence of store depletion, in structural extension and CAD/SOAR exposure of STIM1 R304W leading to constitutive CRAC channel activation and Stormorken disease.
Department of Medical Biophysics University of Toronto Toronto ON M5G 1L7 Canada
Department of Physiology and Pharmacology University of Western Ontario London ON N6A 5C1 Canada
Institute of Biophysics Johannes Kepler University Linz Gruberstrasse 40 4020 Linz Austria
Princess Margaret Cancer Center University Health Network Toronto ON M5G 1L7 Canada
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