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dc.contributor.authorCollado, Javier-
dc.contributor.authorKalemanov, Maria-
dc.contributor.authorCampelo, Felix-
dc.contributor.authorBourgoint, Clelia-
dc.contributor.authorThomas, Ffion-
dc.contributor.authorLoewith, Robbie-
dc.contributor.authorMartínez Sánchez, Antonio-
dc.contributor.authorBaumeister, Wolgang-
dc.contributor.authorStefan, Christopher J.-
dc.contributor.authorFernandez-Busnadiego, Ruben-
dc.date.accessioned2025-01-18T19:35:36Z-
dc.date.available2025-01-18T19:35:36Z-
dc.identifier.citationDevelopmental Cell, Volume 51, Issue 4, 476 - 487.e7es
dc.identifier.issnPrint: 1534-5807-
dc.identifier.issnElectronic: 1878-1551-
dc.identifier.urihttp://hdl.handle.net/10201/148765-
dc.description© 2019, The Author(s). This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/. This document is the Submitted version of a Published Work that appeared in final form in Developmental Cell. To access the final edited and published work see https://doi.org/10.1016/j.devcel.2019.10.018-
dc.description.abstractMembrane 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.-
dc.formatapplication/pdfes
dc.languageenges
dc.publisherElsevier-
dc.relationJ.C. and M.K. were supported by the Graduate School of Quantitative Biosciences Munich. J.C., M.K., A.M.-S., W.B. and R.F.-B. have received funding from the European Commission (FP7 GA ERC-2012-SyG_318987–ToPAG). R.F.-B. acknowledges funding from the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) through Germany’s Excellence Strategy - EXC 2067/1- 390729940 and SFB1190/P22. F.C. acknowledges financial support from the Spanish Ministry of Economy and Competitiveness (“Severo Ochoa” program for Centres of Excellence in R&D (SEV-2015-0522, FIS2015-63550-R, FIS2017-89560-R, BFU2015-73288-JIN, RYC-2017-22227, and AEI/FEDER/UE), Fundació Privada Cellex, and from the Generalitat de Catalunya through the CERCA program. R.L. acknowledges funding from the European Commission (ERC AdG TENDO - 834394), the Swiss National Science Foundation (31003A_179517), the Swiss National Centre for Competence in Research in Chemical Biology (51NF40-185898), and the Canton of Geneva. C.J.S. is supported by MRC funding to the MRC LMCB University Unit at UCL, award code MC_UU_00012/6.es
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectMembrane contact site-
dc.subjectEndoplasmic reticulum-
dc.subjectPlasma membrane-
dc.subjectTricalbins-
dc.subjectMembrane curvature-
dc.subjectCryo‐electron tomography-
dc.titleTricalbin-Mediated contact sites control ER curvature to maintain plasma membrane integrityes
dc.typeinfo:eu-repo/semantics/articlees
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S1534580719308652?via%3Dihub-
dc.identifier.doihttps://doi.org/10.1016/j.devcel.2019.10.018-
dc.contributor.departmentIngeniería de la Información y las Comunicaciones-
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