Počet záznamů: 1  

Potential of correlative luminescence and electron microscopy for detection and location of individual molecules in cells

  1. 1.
    SYSNO ASEP0438715
    Druh ASEPA - Abstrakt
    Zařazení RIVZáznam nebyl označen do RIV
    Zařazení RIVNení vybrán druh dokumentu
    NázevPotential of correlative luminescence and electron microscopy for detection and location of individual molecules in cells
    Tvůrce(i) Klepárník, Karel (UIACH-O) RID, ORCID
    Celkový počet autorů1
    Zdroj.dok.20th International workshop on "Single Molecule Spectroscopy and Ultrasensitive Analysis in the Life Sciences". Program and Abstract Book.. - : PiCoQuant GmbH, 2014
    S. 128-128
    Poč.str.1 s.
    Forma vydáníTištěná - P
    AkceInternational workshop on "Single Molecule Spectroscopy and Ultrasensitive Analysis in the Life Sciences" /20./
    Datum konání02.09.2015-05.09.2015
    Místo konáníBerlin-Adlershof
    ZeměDE - Německo
    Typ akceWRD
    Jazyk dok.eng - angličtina
    Země vyd.DE - Německo
    Klíč. slovaelectron microscopy ; individual molecules ; cell
    Vědní obor RIVCB - Analytická chemie, separace
    CEPGA14-28254S GA ČR - Grantová agentura ČR
    Institucionální podporaUIACH-O - RVO:68081715
    AnotaceRapidly growing field of correlative light and electron microscopy (CLEM) overcomes some drawbacks of EM together with a time consuming process of the localization of studied structures. This technique bridges the functionality of LM with the high resolution of EM. The dynamic data from an optical source are correlated with ultrastructural analysis done by EM by rendering an overlay image of the same area of the specimen. In the last few years, CLEM has become a unique tool for the investigation of relations between a structure and its biological function. The possibility to reliably map locations of receptors (or any protein) onto a cellular surface with a nanometer accuracy has initiated a tremendous interest in this technique. Usually, a specific antibody is conjugated with a high electron density luminophore nanoparticle to form a probe for tracing cellular objects. Under LM, the luminescence image shows the regions of interest and/or functional changes. Subsequently, an electron beam reveals examined structures highlighted by the nanoparticle dots with the nanometer resolution. A unique approach takes advantage of cathodoluminescence of quantum dots (QD). Electron beam excites QD similarly as a laser and the luminescence emission is detected using a sensitive light detector in the same device. Our investigation is focused on two transmembrane proteins, Fas receptor and Fas ligand. These membrane receptors switch the external apoptotic pathways typical for surveillance strategies of the immune system.
    PracovištěÚstav analytické chemie
    KontaktIveta Drobníková, drobnikova@iach.cz, Tel.: 532 290 234
    Rok sběru2015
Počet záznamů: 1  

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