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Quantifying protein densities on cell membranes using super-resolution optical fluctuation imaging

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F17%3A00482642" target="_blank" >RIV/61388955:_____/17:00482642 - isvavai.cz</a>

  • Alternative codes found

    RIV/68378050:_____/17:00482642 RIV/68407700:21230/17:00315471

  • Result on the web

    <a href="http://dx.doi.org/10.1038/s41467-017-01857-x" target="_blank" >http://dx.doi.org/10.1038/s41467-017-01857-x</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1038/s41467-017-01857-x" target="_blank" >10.1038/s41467-017-01857-x</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Quantifying protein densities on cell membranes using super-resolution optical fluctuation imaging

  • Original language description

    Quantitative approaches for characterizing molecular organization of cell membrane molecules under physiological and pathological conditions profit from recently developed super-resolution imaging techniques. Current tools employ statistical algorithms to determine clusters of molecules based on single-molecule localization microscopy (SMLM) data. These approaches are limited by the ability of SMLM techniques to identify and localize molecules in densely populated areas and experimental conditions of sample preparation and image acquisition. We have developed a robust, model-free, quantitative clustering analysis to determine the distribution of membrane molecules that excels in densely labeled areas and is tolerant to various experimental conditions, i.e. multiple-blinking or high blinking rates. The method is based on a TIRF microscope followed by a super-resolution optical fluctuation imaging (SOFI) analysis. The effectiveness and robustness of the method is validated using simulated and experimental data investigating nanoscale distribution of CD4 glycoprotein mutants in the plasma membrane of T cells.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10608 - Biochemistry and molecular biology

Result continuities

  • Project

    <a href="/en/project/GA15-06989S" target="_blank" >GA15-06989S: Organisation and function of CD4 co-receptor on the surface of T cells at nanoscale</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2017

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Nature Communications

  • ISSN

    2041-1723

  • e-ISSN

  • Volume of the periodical

    8

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    7

  • Pages from-to

  • UT code for WoS article

    000416229300017

  • EID of the result in the Scopus database

    2-s2.0-85035071940