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Spinning disk-based superresolution microscopy for subdiffraction structured illumination imaging of living cells

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    SYSNO ASEP0517466
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JOstatní články
    TitleSpinning disk-based superresolution microscopy for subdiffraction structured illumination imaging of living cells
    Author(s) Lunov, Oleg (FZU-D) ORCID
    Smolková, Barbora (FZU-D) ORCID
    Lynnyková, Anna (FZU-D) RID
    Uzhytchak, Mariia (FZU-D) ORCID
    Kubinová, Šárka (FZU-D) RID, ORCID
    Dejneka, Alexandr (FZU-D) RID, ORCID
    Number of authors6
    Source TitleJemná mechanika a optika. - : Fyzikální ústav AV ČR, v. v. i. - ISSN 0447-6441
    Roč. 64, č. 5 (2019), s. 127-129
    Number of pages3 s.
    Publication formPrint - P
    Languageeng - English
    CountryCZ - Czech Republic
    Keywordssuperresolution microscopy ; structured illumination microscopy (SIM) ; lysosomes ; mitochondria
    Subject RIVBO - Biophysics
    OECD categoryBiophysics
    R&D ProjectsLO1409 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Method of publishingLimited access
    Institutional supportFZU-D - RVO:68378271
    AnnotationSuperresolution microscopy enables to see previously hidden details of cellular structures. However, it requires to use high irradiation intensities that may cause artefacts and photodamage of fragile biological samples. Newly developed confocal technique and Olympus super resolution (OSR), that combines spinning disk confocal with structured illumination microscopy, represents a reliable and fast superresolution avoiding photodamage. We demonstrate an OSR microscope platform, that enables subsecond, multicolour data acquisition. It also provides access to subdiffraction structured illumination imaging. We show that OSR allows live-cell experiments without any noticeable cellular damage. OSR system has an improved lateral (∼2) and axial (∼3) resolution compared with conventional confocal imaging. Moreover, OSR is compatible with both fixed and live cell imaging.
    WorkplaceInstitute of Physics
    ContactKristina Potocká, potocka@fzu.cz, Tel.: 220 318 579
    Year of Publishing2020
    Electronic addresshttps://jmo.fzu.cz/sites/jmo.fzu.cz/files/oldweb/2019/2019-05/jmo_19_05_obsah.pdf
Number of the records: 1  

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