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Projekt Druckansicht

Laser scanning confocal microscopy system

Fachliche Zuordnung Grundlagen der Biologie und Medizin
Förderung Förderung in 2010
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 193122643
 
Erstellungsjahr 2014

Zusammenfassung der Projektergebnisse

In the last three years, the confocal microscope became an integral and indispensible part of a variety of projects within and outside of our department. Its usage includes a variety of live cells applications and conventional fixed specimen imaging. Internal and external users belonging to multiple departments and disciplines (Physics, Chemistry, Biology) use the system for their research projects. One of the key research in which the instrument has contributed very significantly is our interdisciplinary DFG funded research college 1657 „Molecular and cellular responses to ionizing radiation”. This is part of our department’s research focus on biology of stress responses (http://www.bio.tudarmstadt.de/ag/forschen/schwerpunkte.en.jsp) and includes groups working on microorganisms, to plants and humans. Animal models as well as cellular models are employed here to elucidate the basis of chromosome stability in normal proliferating cells as well as tumor cells and in response to different types of stress, including radiation stress use in therapy. One o the focus here has been to study the kinetics of DNA damage and its repair using live cell imaging combined with laser microirradiation. Other research areas cover the response of cells and organs to exogenous signals and the signal reception at the level of the cell membrane. As a counterpoint also synthetic membranes assembled into artificial vesicles have been analyzed. To improve drug delivery, collaborative projects in the interface between chemistry and biology have used live-cell microscopy to quantify the kinetics of uptake of drugs as well as their function in vivo. In several of the above mentioned research projects, dynamic live cell measurements have been performed and include: fluorescence photobleaching and photoactivation techniques, laser microbeam irradiation and ratiometric measurements (e.g., of radical oxygen species). These experiments have encompassed from synthetic artificial vesicles, stretched DNA molecules, to bacterial microfilms, insects, plants and mammalian cells and organisms. This is made possible by to the large variety of objectives at the microscope, from very low to the highest magnification. In addition, very complex live-cell imaging experiments (already described in the application) have been successfully performed, which is feasible due to the multiple software modules purchased with the system. Our present directions expand into multi color superresolution light microscopy in fixed and living cells to bridge the gap to electron microscopy.

Projektbezogene Publikationen (Auswahl)

 
 

Zusatzinformationen

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