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ABSTRACTS – ORAL PRESENTATIONS - AMCA, spol. s r.o.

ABSTRACTS – ORAL PRESENTATIONS - AMCA, spol. s r.o.

ABSTRACTS – ORAL PRESENTATIONS - AMCA, spol. s r.o.

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The pore-forming activity of DDHR was investigated on individual giant unilamellar<br />

phospholipid vesicles (GUVs) made of 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC)<br />

and DOPC with 30% content of cholesterol. Using multiphoton fluorescence microscopy<br />

we observed formations of necklace-shaped structures or internal small particles inside<br />

GUVs made of DOPC. This behaviour is consistent with the theory of pore formation<br />

as mode of action explaining the bioactivity of some particular secondary metabolites<br />

(Zemel at al., 2005). Content of cholesterol in GUVs inhibits formation of these structures.<br />

Permeability of membranes after treatment with DDHR was proved in the standard dye<br />

leakage assay performed on the same vesicle types.<br />

We have also proved the direct interaction between cholesterol and DDHR using<br />

FTIR spectroscopy. This interaction could play a crucial role in its bioactivity and<br />

the ability to stain only certain membrane components in cells.<br />

Acknowledgements<br />

This work was supported by Long-Term Research Plans of the Ministry of Education,<br />

Youth and Sports of the Czech Republic No. MSM0021620858. Author is thankful to<br />

the laboratory of RNDr. Miroslav Flieger, CSc., Institute of Microbiology, Academy<br />

of Sciences of the Czech Republic.<br />

References<br />

Berdy, J. (2005). Bioactive Microbial Metabolites. The Journal of Antibiotics, 58(1):<br />

1-26.<br />

Savic, M., Bratic, I., & Vasiljevic, B. (2007). Streptomyces durmitorensis sp. nov., a<br />

producer of an FK506-like immunosuppressant. International journal of systematic and<br />

evolutionary microbiology, 57(Pt 9): 2119-24.<br />

Stodulková, E., Kuzma, M., Hench, I. B., Černý, J., Králová, J., Novák, P., Chudíčková,<br />

M., et al. (2011). New polyene macrolide family produced by submerged culture of<br />

Streptomyces durmitorensis. The Journal of antibiotics, 64(11): 717-22.<br />

Zemel, A., Ben-Shaul, A., May, S. (2005). Perturbation of a lipid membrane by amphipathic<br />

peptides and its role in pore formation. European biophysics journal, 34(3): 230-42.<br />

P12. MODULATION OF HYPERICIN-MEDIATED PHOTODYNAMIC THERAPY USING<br />

HISTONE DEACETYLASE INHIBITORS<br />

Ján Kovaľ, Andrea Halaburková, Rastislav Jendželovský, Jaromír Mikeš, Peter Fedoročko<br />

P. J. Šafárik University in Košice, Faculty of Science, Institute of Biology and Ecology,<br />

Košice, Slovak Republic; jan.koval@upjs.sk<br />

Photodynamic therapy (PDT) is a minimally invasive cancer treatment method which<br />

utilizes different tumor-localizing agents that are activated by irradiation with light<br />

of a specific wavelength. This triggers production of reactive oxygen species, which<br />

subsequently activate processes implicated in irreversible changes to various cellular<br />

targets leading to cell death (Dougherty et al., 1998). Hypericin (HY), a naturally occurring<br />

aromatic polycyclic diantraquinone from St. John’s wort (Hypericum perforatum L.), has<br />

unique photocytotoxic properties suitable for PDT.<br />

Analytical Cytometry VII 101

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