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.: Home > International Journal of Medical Sciences > 2009 > Volume 6 Number 6 > Waldemar Waldeck1, Gabriele Mueller1, Manfred Wiessler2, Manuela Brom3, Katalin Tَth1 and Klaus Braun2

Autofluorescent Proteins as Photosensitizer in Eukaryontes

Waldemar Waldeck1, Gabriele Mueller1, Manfred Wiessler2, Manuela Brom3, Katalin Tَth1 and Klaus Braun2
1. German Cancer Research Center, Dept. of Biophysics of Macromolecules, INF 580, D-69120 Heidelberg, Germany 2. German Cancer Research Center, Dept. of Medical Physics in Radiology, INF 280, D-69120 Heidelberg, Germany 3. German Cancer Research Center, Core Facility Light Microscopy, INF 581, D-69120 Heidelberg, Germany
Abstract :

Since the discovery of the green fluorescent green protein (GFP) in 1961 many variants of fluorescent proteins (FP) were detected. The importance was underlined by the Nobel price award in chemistry 2008 for the invention, application, and development of the GFP by Shimomura, Chalfie and Tsien. GFP, first described by Shimomura now is indispensible in the scientific daily life. Since then and also in future fluorescent proteins will lead to new applications as reporters in cell biology. Such FPs can absorb visible day-light and predominantly one variant of the red fluorescent protein, the KillerRed protein (KRED) emits active electrons producing reactive oxygen species (ROS) leading to photokilling processes in eukaryotes. KRED can be activated by daylight as a photosensitizing agent. It is quite obvious that the KRED’s expression and localization is critical with respect to damage, mutation and finally killing of eukaryotic
cells. We found evidence that the KRED’s cytotoxicity is ascendantly location-dependent from the cell membrane over the nuclear lamina to the chromatin in the cell nucleus. Daylight illumination of cells harbouring the KRED protein fused with the histone H2A, a DNA-binding protein which is critical for the formation of the chromatin structure results in cell killing. Therefore the H2A-KRED fusion protein can be considered as an appropriate candidate for the photodynamic therapy (PDT). This finding can be transferred to current photodynamic approaches and can enhance their therapeutic outcome.

Keywords :
Melanoma; fluorescent Proteins; KillerRed; Photo-Dynamic-Therapy (PDT); ROS; Skin Tumors; subcellular Localization; topical Application

Date Deposited : 28 Jul 2011 10:06

Last Modified : 28 Jul 2011 10:06

Official URL: http://www.medsci.org/archive

Volume 6, Number 6, - 2009 , ISSN 1449-1907

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