VAP proteins – From organelle tethers to pathogenic host interactors and their role in neuronal disease
dc.contributor.author | Kors, S | |
dc.contributor.author | Costello, JL | |
dc.contributor.author | Schrader, M | |
dc.date.accessioned | 2022-04-25T15:13:25Z | |
dc.date.issued | 2022 | |
dc.date.updated | 2022-04-25T14:20:01Z | |
dc.description.abstract | Vesicle-associated membrane protein (VAMP)-associated proteins (VAPs) are ubiquitous ER-resident tail-anchored membrane proteins in eukaryotic cells. Their N-terminal major sperm protein (MSP) domain faces the cytosol and allows them to interact with a wide variety of cellular proteins. Therefore, VAP proteins are vital to many cellular processes, including organelle membrane tethering, lipid transfer, autophagy, ion homeostasis and viral defence. Here, we provide a timely overview of the increasing number of VAPA/B binding partners and discuss the role of VAPA/B in maintaining organelle-ER interactions and cooperation. Furthermore, we address how viruses and intracellular bacteria hijack VAPs and their binding partners to induce interactions between the host ER and pathogen-containing compartments and support pathogen replication. Finally, we focus on the role of VAP in human disease and discuss how mutated VAPB leads to the disruption of cellular homeostasis and causes amyotrophic lateral sclerosis. | en_GB |
dc.description.sponsorship | Biotechnology & Biological Sciences Research Council (BBSRC) | en_GB |
dc.description.sponsorship | Medical Research Council (MRC) | en_GB |
dc.identifier.citation | Awaiting citation and DOI | en_GB |
dc.identifier.grantnumber | BB/V018167/1 | en_GB |
dc.identifier.grantnumber | BB/T002255/1 | en_GB |
dc.identifier.grantnumber | MR/N0137941/1 | en_GB |
dc.identifier.uri | http://hdl.handle.net/10871/129452 | |
dc.identifier | ORCID: 0000-0003-2146-0535 (Schrader, Michael) | |
dc.language.iso | en | en_GB |
dc.publisher | Frontiers Media | en_GB |
dc.rights.embargoreason | Under temporary indefinite embargo pending publication by Frontiers Media. No embargo required on publication. AAM to be replaced with published version on publication | en_GB |
dc.rights | © 2022. This version is made available under the CC-BY 4.0 license: https://creativecommons.org/licenses/by/4.0/ | en_GB |
dc.subject | VAPA | en_GB |
dc.subject | VAPB | en_GB |
dc.subject | FFAT motif | en_GB |
dc.subject | endoplasmic reticulum | en_GB |
dc.subject | membrane contact sites | en_GB |
dc.subject | pathogen-host interactions | en_GB |
dc.subject | amyotrophic lateral sclerosis | en_GB |
dc.title | VAP proteins – From organelle tethers to pathogenic host interactors and their role in neuronal disease | en_GB |
dc.type | Article | en_GB |
dc.date.available | 2022-04-25T15:13:25Z | |
dc.identifier.issn | 2296-634X | |
dc.description | This is the author accepted manuscript. | en_GB |
dc.description | Data availability statement: All datasets generated for this study are included in the article. | en_GB |
dc.identifier.journal | Frontiers in Cell and Developmental Biology | en_GB |
dc.relation.ispartof | Frontiers in Cell and Developmental Biology | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | en_GB |
dcterms.dateAccepted | 2022-04-25 | |
rioxxterms.version | AM | en_GB |
rioxxterms.licenseref.startdate | 2022-04-25 | |
rioxxterms.type | Journal Article/Review | en_GB |
refterms.dateFCD | 2022-04-25T14:20:04Z | |
refterms.versionFCD | AM | |
refterms.panel | A | en_GB |
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