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Approach to map nanotopography of cell surface receptors

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F22%3A00555456" target="_blank" >RIV/61388955:_____/22:00555456 - isvavai.cz</a>

  • Alternative codes found

    RIV/68378050:_____/22:00579083

  • Result on the web

    <a href="http://hdl.handle.net/11104/0329971" target="_blank" >http://hdl.handle.net/11104/0329971</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1038/s42003-022-03152-y" target="_blank" >10.1038/s42003-022-03152-y</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Approach to map nanotopography of cell surface receptors

  • Original language description

    Cells communicate with their environment via surface receptors, but nanoscopic receptor organization with respect to complex cell surface morphology remains unclear. This is mainly due to a lack of accessible, robust and high-resolution methods. Here, we present an approach for mapping the topography of receptors at the cell surface with nanometer precision. The method involves coating glass coverslips with glycine, which preserves the fine membrane morphology while allowing immobilized cells to be positioned close to the optical surface. We developed an advanced and simplified algorithm for the analysis of single-molecule localization data acquired in a biplane detection scheme. These advancements enable direct and quantitative mapping of protein distribution on ruffled plasma membranes with near isotropic 3D nanometer resolution. As demonstrated successfully for CD4 and CD45 receptors, the described workflow is a straightforward quantitative technique to study molecules and their interactions at the complex surface nanomorphology of differentiated metazoan 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

    30102 - Immunology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2022

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Communications Biology

  • ISSN

    2399-3642

  • e-ISSN

    2399-3642

  • Volume of the periodical

    5

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    16

  • Pages from-to

    218

  • UT code for WoS article

    000766635700001

  • EID of the result in the Scopus database

    2-s2.0-85126077799