National Repository of Grey Literature 24 records found  1 - 10nextend  jump to record: Search took 0.00 seconds. 
New antimcrobial peptides isolated from the bee venom and the study of their action mechanism
Čujová, Sabína ; Čeřovský, Václav (advisor) ; Fusek, Martin (referee) ; Hlaváček, Jan (referee)
EN The growing emergence of bacteria resistant to conventional antibiotics is very alarming. This has prompted an intensive search for alternative antimicrobial agents which kill bacteria with different modes of action than do traditional antibiotics and do not develop drug resistance. Among these, antimicrobial peptides (AMPs) are considered as promising compounds against resistant pathogens. These positively charged peptides permeabilize or disrupt bacterial cell envelope which leads to leakage of cytoplasmic components and cell death. The aim of my dissertation thesis was the study of the action mechanism of novel antimicrobial peptides which I have isolated from the venom of different wild bees. I identified six novel AMPs which were named panurgines (PNG), codesane (COD) and antapines (ANTPs). These peptides were isolated from the venom of three different bee species (Panurgus calcaratus, Collete daviesanus and Anthophora plumipes). I was also involved in the structural studies of lasiocepsin (Las), the antimicrobial peptide identified in the venom earlier in our laboratory. All studied peptides possess activity against various strains of bacteria and low or moderate hemolytic activity. We prepared series of PNG, COD and ANTP analogs in order to study the effect of physicochemical properties...
Antimicrobial peptides isolated from the venom of hymenopterous insect
Monincová, Lenka ; Čeřovský, Václav (advisor) ; Macek, Tomáš (referee) ; Fusek, Martin (referee)
Rapid development of bacterial resistance and multiresitance to conventional antibiotics has resulted in an intensive search for alternative antimicrobial agents. Antimicrobial peptides (AMPs) belong to promising anti-infective candidates since they do not development bacterial resistance. They kill microbes by disturbing or permeabilizing the cytoplasmic membrane, or may target putative key intracellular compartments. Their advantages include fast action and selectivity between prokaryotic and eukaryotic cells. We have isolated several novel AMPs from the venom of wild bees: halictines (HAL-1 and HAL-2) from Halictus sexcinctus, lasiocepsin (Las) from Lasioglossum laticeps and macropin (MAC-1) from Macropis fulvipes. They are active against Gram-positive and Gram- negative bacteria and against yeast Candida albicans. While halictines and macropin have moderate hemolytic activity, Las shows no hemolytic activity. A novel AMP was isolated also from the mucus of Xiphydria camelus. This AMP belongs to the category of insect defensins. It contains 55 amino acid residues, three disulphide bridges and its C-terminus is amidated. CD and NMR studies of HAL-1, HAL-2 and MAC-1 revealed propensity to form amphipathic α-helical structure in the presence of sodium dodecyl sulfate or trifluoroethanol. For the...
New antimcrobial peptides isolated from the bee venom and the study of their action mechanism
Čujová, Sabína ; Čeřovský, Václav (advisor) ; Fusek, Martin (referee) ; Hlaváček, Jan (referee)
EN The growing emergence of bacteria resistant to conventional antibiotics is very alarming. This has prompted an intensive search for alternative antimicrobial agents which kill bacteria with different modes of action than do traditional antibiotics and do not develop drug resistance. Among these, antimicrobial peptides (AMPs) are considered as promising compounds against resistant pathogens. These positively charged peptides permeabilize or disrupt bacterial cell envelope which leads to leakage of cytoplasmic components and cell death. The aim of my dissertation thesis was the study of the action mechanism of novel antimicrobial peptides which I have isolated from the venom of different wild bees. I identified six novel AMPs which were named panurgines (PNG), codesane (COD) and antapines (ANTPs). These peptides were isolated from the venom of three different bee species (Panurgus calcaratus, Collete daviesanus and Anthophora plumipes). I was also involved in the structural studies of lasiocepsin (Las), the antimicrobial peptide identified in the venom earlier in our laboratory. All studied peptides possess activity against various strains of bacteria and low or moderate hemolytic activity. We prepared series of PNG, COD and ANTP analogs in order to study the effect of physicochemical properties...
Capillary electrophoretic separation and structure-mobility relationship study of cyclic antimicrobial peptides
Tůmová, Tereza ; Monincová, Lenka ; Čeřovský, Václav ; Kašička, Václav
Capillary electrophoresis (CE) has been employed for qualitative and quantitative analysis, separation and physicochemical characterization of antimicrobial peptides isolated from the venom of eusocial bee Lassioglossum laticeps. From the CE experiments at various pH, the important physico-chemical parameters of analyzed peptides, effective mobilities and acidity constants were determined and the structure-mobility relationships of peptides with variable intramolecular cyclization of their molecules were investigated.
Chiroptical spectroscopy as a sensitive tool for the conformational analysis of antimicrobial peptides
Kocourková, L. ; Novotná, P. ; Čujová, Sabína ; Čeřovský, Václav ; Urbanová, M. ; Setnička, V.
We tested the utilization of electronic and vibrational circular dichroism for the conformational study of antimicrobial peptides on two examples: melectin and antapin in different solutions of liposomes and micelles mimicking bacterial or eukaryotic membranes. The results show significant content of the alpha-helical conformation in an environment mimicking the bacterial membrane, while it was considerably low in the eukaryotic membrane-mimicking environment.
Analysis and characterization of antimicrobial peptides by capillary electromigration methods
Tůmová, Tereza ; Monincová, Lenka ; Čeřovský, Václav ; Kašička, Václav
High-performance capillary electromigration methods (zone electrophoresis, affinity electrophoresis, isotachophoresis and micellar electrokinetic chromatography) have been applied to analysis and physicochemical characterization of halictines – antimicrobial peptides isolated from the bee Halictus sexcinctus.
Analysis and characterization of antimicrobial peptides by capillary electrophoresis
Tůmová, Tereza ; Monincová, Lenka ; Čeřovský, Václav ; Kašička, Václav
Capillary electrophoresis has been employed for quantitative and qualitative analysis, separation and characterization of antimicrobial peptides – halictines. In addition to purity degree of synthetic peptides, also their effective and ionic mobilities and charges within a wide pH range were determined.
Real time in vivo monitoring of cytotoxic activity of two different antimicrobial peptides lasioglossin III and lasiocepsin
Tůmová, Tereza ; Lovecká, P. ; Čeřovský, Václav ; Slaninová, Jiřina
Real-time cell analyzer dual-plate (RTCA DP) can be used to dynamically test the cytotoxic activity of potent antimicrobial peptides. In this study, we tested the activity of two different antimicrobial peptides isolated from venom reservoirs of a wild bee against normal mammalian cell line – rat intestinal epithelial cells. The cytotoxic effect monitored by RTCA DP was expressed as IC50 and compared with the results of standard cytotoxic tests.
Interaction of lasioglossin III with CCRF-CEM cells
Slaninová, Jiřina ; Mlsová, V. ; Günterová, Jana ; Borovičková, Lenka ; Čeřovský, Václav
Antimicrobial peptides isolated recently from the venom reservoirs of wild bees are active not only against bacteria and fungi, but also selectively lyze some cancer cell lines. At the same time they have very low hemolytic activity and concentrations required to lyze control normal cell lines are much higher. Here we describe the time course of the effect of lasioglossin III (LL-III) on CCRF-CEM cells alone and in the mixture with human red blood cells using flow cytometry.

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