dc.contributor.author | Beer, KB | |
dc.contributor.author | Fazeli, G | |
dc.contributor.author | Judasova, K | |
dc.contributor.author | Irmisch, L | |
dc.contributor.author | Causemann, J | |
dc.contributor.author | Mansfeld, J | |
dc.contributor.author | Wehman, AM | |
dc.date.accessioned | 2020-08-12T11:46:38Z | |
dc.date.issued | 2019-08-02 | |
dc.identifier.citation | Nature communications, 2019, 10 (1), pp. 3490 - ? | |
dc.identifier.issn | 2041-1723 | |
dc.identifier.uri | https://repository.icr.ac.uk/handle/internal/3939 | |
dc.identifier.eissn | 2041-1723 | |
dc.identifier.doi | 10.1038/s41467-019-11442-z | |
dc.description.abstract | Visualization of specific organelles in tissues over background fluorescence can be challenging, especially when reporters localize to multiple structures. Instead of trying to identify proteins enriched in specific membrane-wrapped structures, we use a selective degradation approach to remove reporters from the cytoplasm or nucleus of C. elegans embryos and mammalian cells. We demonstrate specific labelling of organelles using degron-tagged reporters, including extracellular vesicles, as well as individual neighbouring membranes. These degron-tagged reporters facilitate long-term tracking of released cell debris and cell corpses, even during uptake and phagolysosomal degradation. We further show that degron protection assays can probe the topology of the nuclear envelope and plasma membrane during cell division, giving insight into protein and organelle dynamics. As endogenous and heterologous degrons are used in bacteria, yeast, plants, and animals, degron approaches can enable the specific labelling and tracking of proteins, vesicles, organelles, cell fragments, and cells in many model systems. | |
dc.format | Electronic | |
dc.format.extent | 3490 - ? | |
dc.language | eng | |
dc.language.iso | eng | |
dc.publisher | NATURE PUBLISHING GROUP | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0 | |
dc.subject | Hela Cells | |
dc.subject | Cell Membrane | |
dc.subject | Embryo, Nonmammalian | |
dc.subject | Animals | |
dc.subject | Humans | |
dc.subject | Caenorhabditis elegans | |
dc.subject | Luminescent Proteins | |
dc.subject | Staining and Labeling | |
dc.subject | Genes, Reporter | |
dc.subject | Fluorescence | |
dc.subject | Proteolysis | |
dc.subject | Extracellular Vesicles | |
dc.subject | Intravital Microscopy | |
dc.title | Degron-tagged reporters probe membrane topology and enable the specific labelling of membrane-wrapped structures. | |
dc.type | Journal Article | |
dcterms.dateAccepted | 2019-07-16 | |
rioxxterms.versionofrecord | 10.1038/s41467-019-11442-z | |
rioxxterms.licenseref.uri | https://creativecommons.org/licenses/by/4.0 | |
rioxxterms.licenseref.startdate | 2019-08-02 | |
rioxxterms.type | Journal Article/Review | |
dc.relation.isPartOf | Nature communications | |
pubs.issue | 1 | |
pubs.notes | Not known | |
pubs.organisational-group | /ICR | |
pubs.organisational-group | /ICR/Primary Group | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Cancer Biology | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Cancer Biology/Post-translational modifications and cell proliferation | |
pubs.organisational-group | /ICR | |
pubs.organisational-group | /ICR/Primary Group | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Cancer Biology | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Cancer Biology/Post-translational modifications and cell proliferation | |
pubs.publication-status | Published | |
pubs.volume | 10 | |
pubs.embargo.terms | Not known | |
icr.researchteam | Post-translational modifications and cell proliferation | |
dc.contributor.icrauthor | Mansfeld, Joerg | |