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Molecular determinants of ER–Golgi contacts identified through a new FRET–FLIM system
ER–TGN contact sites (ERTGoCS) have been visualized by electron microscopy, but their location in the crowded perinuclear area has hampered their analysis via optical microscopy as well as their mechanistic study. To overcome these limits we developed a FRET-based approach and screened several candi...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400564/ https://www.ncbi.nlm.nih.gov/pubmed/30659100 http://dx.doi.org/10.1083/jcb.201812020 |
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author | Venditti, Rossella Rega, Laura Rita Masone, Maria Chiara Santoro, Michele Polishchuk, Elena Sarnataro, Daniela Paladino, Simona D’Auria, Sabato Varriale, Antonio Olkkonen, Vesa M. Di Tullio, Giuseppe Polishchuk, Roman De Matteis, Maria Antonietta |
author_facet | Venditti, Rossella Rega, Laura Rita Masone, Maria Chiara Santoro, Michele Polishchuk, Elena Sarnataro, Daniela Paladino, Simona D’Auria, Sabato Varriale, Antonio Olkkonen, Vesa M. Di Tullio, Giuseppe Polishchuk, Roman De Matteis, Maria Antonietta |
author_sort | Venditti, Rossella |
collection | PubMed |
description | ER–TGN contact sites (ERTGoCS) have been visualized by electron microscopy, but their location in the crowded perinuclear area has hampered their analysis via optical microscopy as well as their mechanistic study. To overcome these limits we developed a FRET-based approach and screened several candidates to search for molecular determinants of the ERTGoCS. These included the ER membrane proteins VAPA and VAPB and lipid transfer proteins possessing dual (ER and TGN) targeting motifs that have been hypothesized to contribute to the maintenance of ERTGoCS, such as the ceramide transfer protein CERT and several members of the oxysterol binding proteins. We found that VAP proteins, OSBP1, ORP9, and ORP10 are required, with OSBP1 playing a redundant role with ORP9, which does not involve its lipid transfer activity, and ORP10 being required due to its ability to transfer phosphatidylserine to the TGN. Our results indicate that both structural tethers and a proper lipid composition are needed for ERTGoCS integrity. |
format | Online Article Text |
id | pubmed-6400564 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64005642019-09-04 Molecular determinants of ER–Golgi contacts identified through a new FRET–FLIM system Venditti, Rossella Rega, Laura Rita Masone, Maria Chiara Santoro, Michele Polishchuk, Elena Sarnataro, Daniela Paladino, Simona D’Auria, Sabato Varriale, Antonio Olkkonen, Vesa M. Di Tullio, Giuseppe Polishchuk, Roman De Matteis, Maria Antonietta J Cell Biol Research Articles ER–TGN contact sites (ERTGoCS) have been visualized by electron microscopy, but their location in the crowded perinuclear area has hampered their analysis via optical microscopy as well as their mechanistic study. To overcome these limits we developed a FRET-based approach and screened several candidates to search for molecular determinants of the ERTGoCS. These included the ER membrane proteins VAPA and VAPB and lipid transfer proteins possessing dual (ER and TGN) targeting motifs that have been hypothesized to contribute to the maintenance of ERTGoCS, such as the ceramide transfer protein CERT and several members of the oxysterol binding proteins. We found that VAP proteins, OSBP1, ORP9, and ORP10 are required, with OSBP1 playing a redundant role with ORP9, which does not involve its lipid transfer activity, and ORP10 being required due to its ability to transfer phosphatidylserine to the TGN. Our results indicate that both structural tethers and a proper lipid composition are needed for ERTGoCS integrity. Rockefeller University Press 2019-03-04 /pmc/articles/PMC6400564/ /pubmed/30659100 http://dx.doi.org/10.1083/jcb.201812020 Text en © 2019 Venditti et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Research Articles Venditti, Rossella Rega, Laura Rita Masone, Maria Chiara Santoro, Michele Polishchuk, Elena Sarnataro, Daniela Paladino, Simona D’Auria, Sabato Varriale, Antonio Olkkonen, Vesa M. Di Tullio, Giuseppe Polishchuk, Roman De Matteis, Maria Antonietta Molecular determinants of ER–Golgi contacts identified through a new FRET–FLIM system |
title | Molecular determinants of ER–Golgi contacts identified through a new FRET–FLIM system |
title_full | Molecular determinants of ER–Golgi contacts identified through a new FRET–FLIM system |
title_fullStr | Molecular determinants of ER–Golgi contacts identified through a new FRET–FLIM system |
title_full_unstemmed | Molecular determinants of ER–Golgi contacts identified through a new FRET–FLIM system |
title_short | Molecular determinants of ER–Golgi contacts identified through a new FRET–FLIM system |
title_sort | molecular determinants of er–golgi contacts identified through a new fret–flim system |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400564/ https://www.ncbi.nlm.nih.gov/pubmed/30659100 http://dx.doi.org/10.1083/jcb.201812020 |
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