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  Tricalbin-Mediated Contact Sites Control ER Curvature to Maintain Plasma Membrane Integrity

Collado, J., Kalemanov, M., Campelo, F., Bourgoint, C., Thomas, F., Loewith, R., et al. (2019). Tricalbin-Mediated Contact Sites Control ER Curvature to Maintain Plasma Membrane Integrity. DEVELOPMENTAL CELL, 51(4), 476-487.e7. doi:10.1016/j.devcel.2019.10.018.

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 Urheber:
Collado, Javier1, Autor           
Kalemanov, Maria1, Autor           
Campelo, Felix2, Autor
Bourgoint, Clelia2, Autor
Thomas, Ffion2, Autor
Loewith, Robbie2, Autor
Martinez Sanchez, Antonio1, Autor           
Baumeister, Wolfgang1, Autor           
Stefan, Christopher J.2, Autor
Fernandez-Busnadiego, Ruben1, Autor           
Affiliations:
1Baumeister, Wolfgang / Molecular Structural Biology, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565142              
2external, ou_persistent22              

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Schlagwörter: CORTICAL ENDOPLASMIC-RETICULUM; CRYOELECTRON TOMOGRAPHY; SACCHAROMYCES-CEREVISIAE; EXTENDED SYNAPTOTAGMINS; PROTEINS; YEAST; ARABIDOPSIS; BINDING; MECHANISMS; LIPIDS
 Zusammenfassung: Membrane contact sites (MCS) between the endoplasmic reticulum (ER) and the plasma membrane (PM) play fundamental roles in all eukaryotic cells. ER-PM MCS are particularly abundant in Saccharomyces cerevisiae, where approximately half of the PM surface is covered by cortical ER (cER). Several proteins, including Ist2, Scs2/22, and Tcb1/2/3 are implicated in cER formation, but the specific roles of these molecules are poorly understood. Here, we use cryo-electron tomography to show that ER-PM tethers are key determinants of cER morphology. Notably, Tcb proteins (tricalbins) form peaks of extreme curvature on the cER membrane facing the PM. Combined modeling and functional assays suggest that Tcb-mediated cER peaks facilitate the transport of lipids between the cER and the PM, which is necessary to maintain PM integrity under heat stress. ER peaks were also present at other MCS, implying that membrane curvature enforcement may be a widespread mechanism to regulate MCS function.

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Sprache(n): eng - English
 Datum: 2019
 Publikationsstatus: Erschienen
 Seiten: 19
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: ISI: 000497127400007
DOI: 10.1016/j.devcel.2019.10.018
 Art des Abschluß: -

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Titel: DEVELOPMENTAL CELL
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: 50 HAMPSHIRE ST, FLOOR 5, CAMBRIDGE, MA 02139 USA : CELL PRESS
Seiten: - Band / Heft: 51 (4) Artikelnummer: - Start- / Endseite: 476 - 487.e7 Identifikator: ISSN: 1534-5807