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dc.contributor.authorDultz, Elisa
dc.contributor.authorWojtynek, Matthias
dc.contributor.authorMedalia, Ohad
dc.contributor.authorOnishchenko, Evgeny
dc.date.accessioned2022-08-05T13:41:59Z
dc.date.available2022-08-05T13:41:59Z
dc.date.created2022-06-09T16:29:47Z
dc.date.issued2022
dc.identifier.issn2073-4409
dc.identifier.urihttps://hdl.handle.net/11250/3010404
dc.description.abstractNuclear pore complexes (NPCs) are the only transport channels that cross the nuclear envelope. Constructed from ~500–1000 nucleoporin proteins each, they are among the largest macromolecular assemblies in eukaryotic cells. Thanks to advances in structural analysis approaches, the construction principles and architecture of the NPC have recently been revealed at submolecular resolution. Although the overall structure and inventory of nucleoporins are conserved, NPCs exhibit significant compositional and functional plasticity even within single cells and surprising variability in their assembly pathways. Once assembled, NPCs remain seemingly unexchangeable in post-mitotic cells. There are a number of as yet unresolved questions about how the versatility of NPC assembly and composition is established, how cells monitor the functional state of NPCs or how they could be renewed. Here, we review current progress in our understanding of the key aspects of NPC architecture and lifecycle.en_US
dc.language.isoengen_US
dc.publisherMDPIen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleThe Nuclear Pore Complex: Birth, Life, and Death of a Cellular Behemothen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2022 The Author(s)en_US
dc.source.articlenumber1456en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.3390/cells11091456
dc.identifier.cristin2030571
dc.source.journalCellsen_US
dc.identifier.citationCells. 2022, 11 (9), 1456.en_US
dc.source.volume11en_US
dc.source.issue9en_US


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