VAŘECHA, Miroslav, Jana AMRICHOVÁ, Michal ZIMMERMANN, Vladimír ULMAN, Marek KAŠÍK and Michal KOZUBEK. Fluorescent microscopy of living cells. In Analytical Cytometry IV: Book of Abstracts. 2007. ISBN 978-80-239-9591-6.
Other formats:   BibTeX LaTeX RIS
Basic information
Original name Fluorescent microscopy of living cells
Name in Czech Fluorescenční mikroskopie živých buněk
Authors VAŘECHA, Miroslav (203 Czech Republic, guarantor), Jana AMRICHOVÁ (203 Czech Republic), Michal ZIMMERMANN (203 Czech Republic), Vladimír ULMAN (203 Czech Republic), Marek KAŠÍK (203 Czech Republic) and Michal KOZUBEK (203 Czech Republic).
Edition Analytical Cytometry IV: Book of Abstracts, 2007.
Other information
Original language English
Type of outcome Conference abstract
Field of Study Genetics and molecular biology
Country of publisher Czech Republic
Confidentiality degree is not subject to a state or trade secret
RIV identification code RIV/00216224:14330/07:00020659
Organization unit Faculty of Informatics
ISBN 978-80-239-9591-6
Keywords in English fluorescence; microscopy; living cells; image analysis
Tags CBIA, fluorescence, Image analysis, living cells, microscopy
Tags International impact, Reviewed
Changed by Changed by: Mgr. Miroslav Vařecha, Ph.D., učo 82780. Changed: 19/10/2010 11:29.
Abstract
Fluorescent protein technology has started by using aequorea victoria fluorescent protein derivatives. These have become the essential tools for the cell biology research. Enhanced green fluorescent protein (EGFP) has been mutated to cyan (ECFP) and yellow (EYFP) fluorescent variants, to allow the simultaneous observation of several protein fusions in live cells especially for co-localization studies and to use the biophysical properties of these fluorophores to detect protein-protein interactions and conformational changes by fluorescence resonance energy transfer (FRET) technique. The discovery and development of red fluorescent protein variants have led to fluorophores that can be distinctly imaged together with other fluorescent proteins to achieve two- or three-color imaging. The practical use of these fluorophores has many challenges: photobleaching of these proteins; signal bleeding due to overlapping emission/excitation spectra; and relatively low amount of fluorescent signal from some of the proteins. Time-lapse microscopy of living cells is especially sensitive to photobleaching due to frequent exposures of sample, cells viability on microscopic stage, and cell movement and changes. In this presentation, we will discuss various experimental methods used in living-cells fluorescent microscopy and we will also discuss numerous challenges and approaches to image analysis of obtained image data. This work is supported by the Grant Agency of the Czech Republic (grant number 204/03/D031) and by The Ministry of Education, Youth and Sports of the Czech Republic (project numbers MSM0021622419 and LC535).
Abstract (in Czech)
Fluorescenční mikroskopie živých buněk
Links
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
LC535, research and development projectName: Dynamika a organizace chromosomů během buněčného cyklu v normě a patologii
Investor: Ministry of Education, Youth and Sports of the CR, Dynamika a organizace chromosomů během buněčného cyklu v normě a patologii
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
PrintDisplayed: 3/5/2024 21:17