VAŘECHA, Miroslav, Jana AMRICHOVÁ, Vladan ONDŘEJ, Emilie LUKÁŠOVÁ, Vladimír ULMAN, Petr MATULA, Michal KOZUBEK and Stanislav KOZUBEK. Imaging of mitochondrial apoptogenic proteins released during apoptosis in living and fixed cells. In Book of Abstracts for 13th Euroconference on Apoptosis. 2005. ISBN 963-219-273-7.
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Basic information
Original name Imaging of mitochondrial apoptogenic proteins released during apoptosis in living and fixed cells.
Name in Czech Sledování mitochondriálních apoptotických proteinů uvolněných během apoptózy v živých a fixovaných buňkách.
Authors VAŘECHA, Miroslav (203 Czech Republic, guarantor), Jana AMRICHOVÁ (203 Czech Republic), Vladan ONDŘEJ (203 Czech Republic), Emilie LUKÁŠOVÁ (203 Czech Republic), Vladimír ULMAN (203 Czech Republic), Petr MATULA (203 Czech Republic), Michal KOZUBEK (203 Czech Republic) and Stanislav KOZUBEK (203 Czech Republic).
Edition Book of Abstracts for 13th Euroconference on Apoptosis, 2005.
Other information
Original language English
Type of outcome Conference abstract
Field of Study Genetics and molecular biology
Country of publisher Belgium
Confidentiality degree is not subject to a state or trade secret
RIV identification code RIV/00216224:14330/05:00013294
Organization unit Faculty of Informatics
ISBN 963-219-273-7
Keywords in English living cells; GFP; fluorescent protein; FRET; fluorescent microscopy
Tags CBIA, fluorescent microscopy, fluorescent protein, FRET, GFP, living cells
Tags International impact, Reviewed
Changed by Changed by: Mgr. Miroslav Vařecha, Ph.D., učo 82780. Changed: 19/10/2010 11:15.
Abstract
Our project is focused on study of mitochondrial apoptogenic proteins released during apoptosis and associated with caspase-independent nuclear chromatin condensation and degradation. We introduce our automated 2D/3D/4D/FRET high-resolution image data acquisition and analysis system developed to visualize and quantify fluorescence signals in fixed and living cells. For our studies, we utilize the fluorescent proteins and various low-toxicity cell permeable fluorescent probes that make it possible to conduct the non-invasive quantitative visualization in living cells. In our experiments, cells are stably or transiently transfected or cotransfected by lipofection with DNA plasmids coding fusion proteins of mitochondrial apoptogenic proteins (cytochrom c, AIF, amid, and endonuclease g) with one of fluorescence proteins (EGFP, EYFP, or t-HcRed).
Abstract (in Czech)
Sledování mitochondriálních apoptotických proteinů uvolněných během apoptózy v živých a fixovaných buňkách.
Links
GA202/04/0907, research and development projectName: Cytometrie s vysokým rozlišením na živých buňkách
Investor: Czech Science Foundation, High-resolution cytometry of living cells
GP204/03/D031, research and development projectName: Apoptózu vyvolávající faktor (AIF): Jeho uvolnění z mitochondrie a změny, které vyvolává ve struktuře jaderného chromatinu
Investor: Czech Science Foundation, Apoptosis-inducing factor (AIF): its translocation from mitochondria and its action on nuclear chromatin
GP204/05/P090, research and development projectName: Topografická a funkční charakteristika telomer v různých typech nádorových buněk stanovená in situ a in vivo
Investor: Czech Science Foundation, Topographic and functional characterization of telomeres in various tumor cell lines determined in situ and in vivo
MSM0021622419, plan (intention)Name: Vysoce paralelní a distribuované výpočetní systémy
Investor: Ministry of Education, Youth and Sports of the CR, Highly Parallel and Distributed Computing Systems
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