Publication:
A new tool based on two micromanipulators facilitates the handling of ultrathin cryosection ribbons

cris.virtual.author-orcid0000-0001-7725-5579
cris.virtualsource.author-orcid349cf5ae-49f5-48c4-b902-24bdbd29d56b
cris.virtualsource.author-orciddd3192fa-2c79-48e8-8703-7ae4724d6319
cris.virtualsource.author-orcide050e437-7048-4ed7-8f07-6eaad53734c2
datacite.rightsopen.access
dc.contributor.authorStuder, Daniel Franz
dc.contributor.authorKlein, Alycia
dc.contributor.authorIacovache, Mircea Ioan
dc.contributor.authorGnaegi, Helmut
dc.contributor.authorZuber, Benoît
dc.date.accessioned2024-10-15T06:12:47Z
dc.date.available2024-10-15T06:12:47Z
dc.date.issued2014-01
dc.description.abstractA close to native structure of bulk biological specimens can be imaged by cryo-electron microscopy of vitreous sections (CEMOVIS). In some cases structural information can be combined with X-ray data leading to atomic resolution in situ. However, CEMOVIS is not routinely used. The two critical steps consist of producing a frozen section ribbon of a few millimeters in length and transferring the ribbon onto an electron microscopy grid. During these steps, the first sections of the ribbon are wrapped around an eyelash (unwrapping is frequent). When a ribbon is sufficiently attached to the eyelash, the operator must guide the nascent ribbon. Steady hands are required. Shaking or overstretching may break the ribbon. In turn, the ribbon immediately wraps around itself or flies away and thereby becomes unusable. Micromanipulators for eyelashes and grids as well as ionizers to attach section ribbons to grids were proposed. The rate of successful ribbon collection, however, remained low for most operators. Here we present a setup composed of two micromanipulators. One of the micromanipulators guides an electrically conductive fiber to which the ribbon sticks with unprecedented efficiency in comparison to a not conductive eyelash. The second micromanipulator positions the grid beneath the newly formed section ribbon and with the help of an ionizer the ribbon is attached to the grid. Although manipulations are greatly facilitated, sectioning artifacts remain but the likelihood to investigate high quality sections is significantly increased due to the large number of sections that can be produced with the reported tool.
dc.description.numberOfPages4
dc.description.sponsorshipInstitut für Anatomie
dc.identifier.doi10.7892/boris.46869
dc.identifier.pmid24269483
dc.identifier.publisherDOI10.1016/j.jsb.2013.11.005
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/118132
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofJournal of structural biology
dc.relation.issn1047-8477
dc.relation.organizationDCD5A442BCD7E17DE0405C82790C4DE2
dc.subjectCryo-electron microscopy Cryosectioning Electron microscopy Frozen-hydrated sections High pressure freezing Micromanipulation Ultramicrotomy
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleA new tool based on two micromanipulators facilitates the handling of ultrathin cryosection ribbons
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPage128
oaire.citation.issue1
oaire.citation.startPage125
oaire.citation.volume185
oairecerif.author.affiliationInstitut für Anatomie
oairecerif.author.affiliationInstitut für Anatomie
oairecerif.author.affiliationInstitut für Anatomie
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
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unibe.description.ispublishedpub
unibe.eprints.legacyId46869
unibe.journal.abbrevTitleJ STRUCT BIOL
unibe.refereedtrue
unibe.subtype.articlejournal

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