Vinculin binding angle in podosomes revealed by high resolution microscopy

dc.bibliographicCitation.firstPagee88251eng
dc.bibliographicCitation.issue2eng
dc.bibliographicCitation.journalTitlePLoS ONEeng
dc.bibliographicCitation.volume9eng
dc.contributor.authorWalde, M.
dc.contributor.authorMonypenny, J.
dc.contributor.authorHeintzmann, R.
dc.contributor.authorJones, G.E.
dc.contributor.authorCox, S.
dc.date.accessioned2020-11-20T17:21:06Z
dc.date.available2020-11-20T17:21:06Z
dc.date.issued2014
dc.description.abstractPodosomes are highly dynamic actin-rich adhesive structures formed predominantly by cells of the monocytic lineage, which degrade the extracellular matrix. They consist of a core of F-actin and actin-regulating proteins, surrounded by a ring of adhesion-associated proteins such as vinculin. We have characterised the structure of podosomes in macrophages, particularly the structure of the ring, using three super-resolution fluorescence microscopy techniques: stimulated emission depletion microscopy, structured illumination microscopy and localisation microscopy. Rather than being round, as previously assumed, we found the vinculin ring to be created from relatively straight strands of vinculin, resulting in a distinctly polygonal shape. The strands bind preferentially at angles between 116° and 135°. Furthermore, adjacent vinculin strands are observed nucleating at the corners of the podosomes, suggesting a mechanism for podosome growth.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://doi.org/10.34657/4567
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/5938
dc.language.isoengeng
dc.publisherSan Francisco, CA : Public Library of Scienceeng
dc.relation.doihttps://doi.org/10.1371/journal.pone.0088251
dc.relation.issn1932-6203
dc.rights.licenseCC BY 3.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/eng
dc.subject.ddc570eng
dc.subject.otheractineng
dc.subject.otherpaxillineng
dc.subject.othertalineng
dc.subject.othervinculineng
dc.subject.otherarticleeng
dc.subject.othercell compositioneng
dc.subject.othercell growtheng
dc.subject.othercell membraneeng
dc.subject.othercell structureeng
dc.subject.othercellular distributioneng
dc.subject.othercontrolled studyeng
dc.subject.othercytoskeletoneng
dc.subject.otherdepletioneng
dc.subject.otherfluorescence microscopyeng
dc.subject.otherhumaneng
dc.subject.otherhuman celleng
dc.subject.otherintermethod comparisoneng
dc.subject.otherlocalisation microscopyeng
dc.subject.othermacrophageeng
dc.subject.otherpodosomeeng
dc.subject.otherprotein bindingeng
dc.subject.otherprotein structureeng
dc.subject.otherstimulated emission depletion microscopyeng
dc.subject.otherstructured illumination microscopyeng
dc.subject.otherActin Cytoskeletoneng
dc.subject.otherActinseng
dc.subject.otherCell Adhesioneng
dc.subject.otherCell Lineeng
dc.subject.otherCell Movementeng
dc.subject.otherHumanseng
dc.subject.otherImage Processing, Computer-Assistedeng
dc.subject.otherMacrophageseng
dc.subject.otherMicroscopyeng
dc.subject.otherMicroscopy, Fluorescenceeng
dc.subject.otherTalineng
dc.subject.otherVinculineng
dc.titleVinculin binding angle in podosomes revealed by high resolution microscopyeng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorIPHTeng
wgl.subjectBiowissenschaften/Biologieeng
wgl.typeZeitschriftenartikeleng
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