3D membrane segmentation and quantification of intact thick cells using cryo soft X-ray transmission microscopy: A pilot study

dc.contributor.authorCárdenes, Rubén
dc.contributor.authorZhang, Chong
dc.contributor.authorKlementieva, Oxana
dc.contributor.authorWerner, Stephan
dc.contributor.authorGuttmann, Peter
dc.contributor.authorPratsch, Christoph
dc.contributor.authorCladera, Josep
dc.contributor.authorBijnens, Bart
dc.date.accessioned2018-09-10T10:15:37Z
dc.date.available2018-09-10T10:15:37Z
dc.date.issued2017-04-04
dc.date.updated2018-07-24T12:08:54Z
dc.description.abstractStructural analysis of biological membranes is important for understanding cell and subcellular organelle function as well as their interaction with the surrounding environment. Imaging of whole cells in three dimension at high spatial resolution remains a significant challenge, particularly for thick cells. Cryo-transmission soft X-ray microscopy (cryo-TXM) has recently gained popularity to image, in 3D, intact thick cells (similar to 10 mu m) with details of subcellular architecture and organization in near-native state. This paper reports a new tool to segment and quantify structural changes of biological membranes in 3D from cryo-TXM images by tracking an initial 2D contour along the third axis of the microscope, through a multi-scale ridge detection followed by an active contours-based model, with a subsequent refinement along the other two axes. A quantitative metric that assesses the grayscale profiles perpendicular to the membrane surfaces is introduced and shown to be linearly related to the membrane thickness. Our methodology has been validated on synthetic phantoms using realistic microscope properties and structure dimensions, as well as on real cryo-TXM data. Results demonstrate the validity of our algorithms for cryo-TXM data analysis.
dc.format.extent22 p.
dc.format.mimetypeapplication/pdf
dc.identifier.pmid28376110
dc.identifier.urihttps://hdl.handle.net/2445/124408
dc.language.isoeng
dc.publisherPublic Library of Science (PLoS)
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1371/journal.pone.0174324
dc.relation.ispartofPLoS One, 2017, vol. 12, num. 4, p. e0174324
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/283570/EU//BIOSTRUCT-X
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/278486/EU//DEVELAGE
dc.relation.urihttps://doi.org/10.1371/journal.pone.0174324
dc.rightscc by (c) Cárdenes et al., 2017
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject.classificationMembranes cel·lulars
dc.subject.classificationRadiografia
dc.subject.otherCell membranes
dc.subject.otherRadiography
dc.title3D membrane segmentation and quantification of intact thick cells using cryo soft X-ray transmission microscopy: A pilot study
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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