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Design and synthesis of specific colevelin derivatives for in vitro and in vivo studies
Kostomoiri, M. ; Zikos, C. ; Benaki, D. ; Slaninová, Jiřina ; Pirmettis, I. ; Papadopoulos, M. ; Pelecanou, M. ; Livaniou, E.
Colivelin is the most potent member of the humanin family of neuroprotective peptides with in vitro and in vivo action against insults associated with Alzeimer’s Disease. The mechanism of action of colivelin is not yet elucidated. The objective of the present study is the design and synthesis of specific colivelin derivatives that can be used as molecular probes in in vitro and in vivo biological experiments. In the frame of the study three colivelin derivatives bearing suitable tags, i.e the fluorescent moiety FITC, the 99mTc-radiometal chelating unit dimethylGly-Ser-Cys, and the streptavidin-counterpart biotinyl-group, were designed and synthesized. These derivatives will be used in in vitro cell component binding and in vivo biodistribution experiments, in order to gain better insight on the mode of the neuroprotective action of colivelin.
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In vitro and in vivo antimicrobial effect of lasioglossins on the Candida albicans
Kašperová, A. ; Turánek, J. ; Čeřovský, Václav ; Raška, M.
Lasioglossins represent a new group of amphipathic α-helical peptides with significant antimicrobial effect on the Candida albicans. This study examines the antifungal activity of two peptides LL-III and all D-LL-III as measured by the suppression of Candida proliferation and suppression of induced morphological differentiation both in in vitro and in vivo assays. In the in vitro Candida proliferation assay, the inhibitory effect of lasioglossins LL-III and all D-LL-III was more than 70% within 24 h and more than 84% after 48 h of incubation (final concentration of either peptide was 17.5 .mu.M). Delaying of blastoconidial transition to hyphae in vitro and tendency to suppress vaginal candidiasis in experimental mice were detected.
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Different charged short lipopeptides
Ježek, R. ; Slaninová, Jiřina ; Králová, M. ; Macková, M.
Series of short peptides palmitoylated in different positions was designed, synthesized and tested for antimicrobial activities. The palmitoyl group was situated either on the alpha - amino group in position 1 or on the epsilon - amino group of lysine in position 3. The peptide charge ranged from –3 to +4. The peptide part of the lipopeptides constituted mainly from lysine, arginine and glutamic acid.
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Lucifensin, a peptide behind the maggot therapy
Čeřovský, Václav
The larvae of the green bottle fly (Lucilia sericata) are routinely used as a medication for the treatment of necrotic, non-healing and highly infected wound in many hospitals all over the world. We have identified and determined primary structure of the defensin originated from the immune system of Lucilia sericata larvae and named it lucifensin. This is 40 amino acid residues and three intramolecular disulfide bridges peptide. The synthetic lucifensin was active against Gram-positive bacteria and was not hemolytic. We studied the importance of lucifensin disulfide bridges and the N-terminal part of its molecule for the structure and for antimicrobial activity.
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Analysis of antimicrobial peptides by capillary electrophoresis
Ehala, Sille ; Niederhafner, Petr ; Čeřovský, Václav ; Řezanka, P. ; Sýkora, D. ; Král, V. ; Kašička, Václav
Capillary electrophoresis was used for the purity degree determination of new antimicrobial peptides: octadecapeptide melectin and tetradecapeptide mastoparan PDD-B, and their synthetic analogues. Besides, four semiempirical models correlating electrophoretic mobilities of these peptides with their charge and size (relative molecular mass) were applied to predict their probable structures in solution. Additionally, capillaries coated with gold nanoparticles were employed for the separation of mixtures of antimicrobial peptides.
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Capillary electrophoresis applied to analysis and characterization of mono-N-acyl-2,6-diaminopimelic acid derivatives
Vítovcová, M. ; Hlaváček, Jan ; Pícha, Jan ; Vaněk, Václav ; Jiráček, Jiří ; Kašička, Václav
Capillary zone electrophoresis and micellar electrokinetic chromatography have been employed for determination of electrophoretic purity degree, limit of detection and limit of quantification of twelve mono-Nacylated derivatives of 2,6-diaminopimelic acid (DAP). In addition, the DAP derivatives were characterized by effective electrophoretic mobilities of their cationic and anionic forms in several classical and isoelectric buffer-based background electrolytes within a broad pH range 2.18 – 8.64.
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