Publication:
Visualization of cell microtubules in their native state.

cris.virtual.author-orcid0000-0001-7725-5579
cris.virtualsource.author-orcide050e437-7048-4ed7-8f07-6eaad53734c2
datacite.rightsrestricted
dc.contributor.authorBouchet-Marquis, Cédric
dc.contributor.authorZuber, Benoît
dc.contributor.authorGlynn, Anne-Marie
dc.contributor.authorEltsov, Mikhail
dc.contributor.authorGrabenbauer, Markus
dc.contributor.authorGoldie, Kenneth N
dc.contributor.authorThomas, Daniel
dc.contributor.authorFrangakis, Achilleas S
dc.contributor.authorDubochet, Jacques
dc.contributor.authorChrétien, Denis
dc.date.accessioned2024-10-23T19:24:05Z
dc.date.available2024-10-23T19:24:05Z
dc.date.issued2007-01
dc.description.abstractBACKGROUND INFORMATION Over the past decades, cryo-electron microscopy of vitrified specimens has yielded a detailed understanding of the tubulin and microtubule structures of samples reassembled in vitro from purified components. However, our knowledge of microtubule structure in vivo remains limited by the chemical treatments commonly used to observe cellular architecture using electron microscopy. RESULTS We used cryo-electron microscopy and cryo-electron tomography of vitreous sections to investigate the ultrastructure of microtubules in their cellular context. Vitreous sections were obtained from organotypic slices of rat hippocampus and from Chinese-hamster ovary cells in culture. Microtubules revealed their protofilament ultrastructure, polarity and, in the most favourable cases, molecular details comparable with those visualized in three-dimensional reconstructions of microtubules reassembled in vitro from purified tubulin. The resolution of the tomograms was estimated to be approx. 4 nm, which enabled the detection of luminal particles of approx. 6 nm in diameter inside microtubules. CONCLUSIONS The present study provides a first step towards a description of microtubules, in addition to other macromolecular assemblies, in an unperturbed cellular context at the molecular level. As the resolution appears to be similar to that obtainable with plunge-frozen samples, it should allow for the in vivo identification of larger macromolecular assemblies in vitreous sections of whole cells and tissues.
dc.description.numberOfPages9
dc.description.sponsorshipInstitut für Anatomie
dc.identifier.doi10.7892/boris.74799
dc.identifier.pmid17049046
dc.identifier.publisherDOI10.1042/BC20060081
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/137205
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofBiology of the cell
dc.relation.issn0248-4900
dc.relation.organizationDCD5A442BCD7E17DE0405C82790C4DE2
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleVisualization of cell microtubules in their native state.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPage53
oaire.citation.issue1
oaire.citation.startPage45
oaire.citation.volume99
oairecerif.author.affiliationInstitut für Anatomie
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.description.ispublishedpub
unibe.eprints.legacyId74799
unibe.refereedtrue
unibe.subtype.articlejournal

Files

Original bundle
Now showing 1 - 1 of 1
Name:
06.Bouchet-Marquis_Visualization_CellMicrotubules_2007.pdf
Size:
911.74 KB
Format:
Adobe Portable Document Format
File Type:
text
License:
publisher
Content:
published

Collections