Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/70184
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dc.contributor.authorHana Antonickaen_US
dc.contributor.authorZhen Yuan Linen_US
dc.contributor.authorAlexandre Janeren_US
dc.contributor.authorMari J. Aaltonenen_US
dc.contributor.authorWoranontee Weraarpachaien_US
dc.contributor.authorAnne Claude Gingrasen_US
dc.contributor.authorEric A. Shoubridgeen_US
dc.date.accessioned2020-10-14T08:25:17Z-
dc.date.available2020-10-14T08:25:17Z-
dc.date.issued2020-09-01en_US
dc.identifier.issn19327420en_US
dc.identifier.issn15504131en_US
dc.identifier.other2-s2.0-85089953070en_US
dc.identifier.other10.1016/j.cmet.2020.07.017en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85089953070&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/70184-
dc.description.abstract© 2020 Elsevier Inc. We used BioID, a proximity-dependent biotinylation assay with 100 mitochondrial baits from all mitochondrial sub-compartments, to create a high-resolution human mitochondrial proximity interaction network. We identified 1,465 proteins, producing 15,626 unique high-confidence proximity interactions. Of these, 528 proteins were previously annotated as mitochondrial, nearly half of the mitochondrial proteome defined by Mitocarta 2.0. Bait-bait analysis showed a clear separation of mitochondrial compartments, and correlation analysis among preys across all baits allowed us to identify functional clusters involved in diverse mitochondrial functions and to assign uncharacterized proteins to specific modules. We demonstrate that this analysis can assign isoforms of the same mitochondrial protein to different mitochondrial sub-compartments and show that some proteins may have multiple cellular locations. Outer membrane baits showed specific proximity interactions with cytosolic proteins and proteins in other organellar membranes, suggesting specialization of proteins responsible for contact site formation between mitochondria and individual organelles.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleA High-Density Human Mitochondrial Proximity Interaction Networken_US
dc.typeJournalen_US
article.title.sourcetitleCell Metabolismen_US
article.volume32en_US
article.stream.affiliationsMcGill University, Montreal Neurological Institute and Hospitalen_US
article.stream.affiliationsUniversity of Torontoen_US
article.stream.affiliationsMcGill Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsLunenfeld-Tanenbaum Research Institute (Toronto)en_US
Appears in Collections:CMUL: Journal Articles

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