Number of the records: 1  

Multi-step synthesis of caspase-3 sensor based on Förster resonance energy transfer

  1. 1.
    SYSNO ASEP0422636
    Document TypeC - Proceedings Paper (int. conf.)
    R&D Document TypeConference Paper
    TitleMulti-step synthesis of caspase-3 sensor based on Förster resonance energy transfer
    Author(s) Lišková, Marcela (UIACH-O)
    Klepárník, Karel (UIACH-O) RID, ORCID
    Pazdera, P. (CZ)
    Foret, František (UIACH-O) RID, ORCID
    Number of authors4
    Source TitleChemické Listy. Roč. 107, Issue s3.. - Praha : Česká společnost chemická, 2013 - ISSN 0009-2770
    Pagess. 315-317
    Number of pages3 s.
    Publication formOnline - E
    ActionCECE Junior 2013
    Event date12.11.2013-13.11.2013
    VEvent locationBrno
    CountryCZ - Czech Republic
    Event typeWRD
    Languageeng - English
    CountryCZ - Czech Republic
    Keywordscaspase-3 ; Förster resonance energy transfer ; apoptotic cells
    Subject RIVCB - Analytical Chemistry, Separation
    R&D ProjectsEE2.3.20.0182 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    GAP301/11/2055 GA ČR - Czech Science Foundation (CSF)
    GBP206/12/G014 GA ČR - Czech Science Foundation (CSF)
    GAP206/11/2377 GA ČR - Czech Science Foundation (CSF)
    Institutional supportUIACH-O - RVO:68081715
    UT WOS000328730800013
    AnnotationProgrammed cell death or apoptosis is regulated process of cell suicide. The central role in apoptosis play cysteine proteases called caspases. Caspases recognize tetra-peptide sequences Asp-Glu-Val-Asp (DEVD) on their substrates and hydrolyze peptide bonds after aspartic acid residues. Various techniques for the determination of caspase-3 are commercially available e.g. Enzyme Linked Immuno-Sorbent Assay (ELISA), Western blotting or flow cytometric analysis. The products of the cleavage can be detected by spectrophotometry, fluorimetry, chemiluminescence (CL) or ELISA. In this work, we suggested fluorescent sensor based on Förster Resonance Energy Transfer (FRET) to determine caspase-3 in cell nucleus or cytoplasm by apoptosis for very fast analysis by fluorescence microscopy without sample destroying.
    WorkplaceInstitute of Analytical Chemistry
    ContactIveta Drobníková, drobnikova@iach.cz, Tel.: 532 290 234
    Year of Publishing2014
Number of the records: 1  

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