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Examination of the Antibacterial and Immunostimulatory Activity of a Wasp Venom PeptideMobley, Yuvon Rondreise January 2013 (has links)
<p>Antimicrobial peptides (AMPs) are part of the innate immune system that is widely distributed in nature, acting as a defense mechanism against invading microorganisms. AMPs have potent antimicrobial activity against a range of microorganisms including fungi, bacteria and viruses. In view of growing multidrug resistance, AMPs are increasingly being viewed as potential therapeutic agents with a novel mechanism of action. Mastoparan is a natural, highly positively charged AMP derived from the venom of wasps. It was originally of interest based on its inherent mast cell degranulation activity. Previously, mastoparan has been shown to exhibit antimicrobial activity in vitro however these studies have been limited in scope. Here we hypothesize that mastoparan possess the capacity to be a potent broad spectrum antibacterial agent including activity against multidrug resistant bacteria. </p><p>We examined the scope of antibacterial activity exhibited by mastoparan using a variety of antimicrobial susceptibility tests and have utilized a bacterial skin infection (S. aureus) model to determine the potential of mastoparan to serve as a therapeutic agent. We tested mastoparan against 4 Gram-positive clinical isolates (e.g., S. aureus, and E. faecium), 9 Gram-negative clinical isolates (e.g., E. coli, P. aeruginosa, and B. cepacia), and 4 multidrug resistant clinical isolates (e.g., MRSA, ESBL E.coli, and ESBL K. pneumonia). These studies reveal that mastoparan exhibits broad spectrum activity against both Gram-negative (MIC: 1.9 - 125 &mug/ml) and Gram-positive (MIC: 15.6 - 125 &mug/ml) bacteria and against multidrug resistant bacteria (MIC: 7.8 - 125 &mug/ml). We also demonstrated that mastoparan disrupts the bacterial membrane, exhibits fast acting antibacterial activity and is highly effective against both multiplying and non-multiplying bacteria. Furthermore, we have shown that mastoparan demonstrates efficacy as a topical antimicrobial agent reducing lesion size by up to 79% and the amount of bacteria recovered from skin lesions by up to a 98% reduction. Based on these results we conclude that mastoparan is a highly effective antibacterial agent and is therefore a potential alternative to currently antibiotics. Mastoparan offers a promising new therapeutic option for treating bacterial infections.</p> / Dissertation
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The Adjuvant Activity and Mechanisms of Action for Mastoparan 7 Peptide After Intranasal Immunization in MiceWanyonyi, Moses Sichangi January 2014 (has links)
<p>No</p> / Dissertation
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Studies on the activation of G proteins by opioid receptors and receptor-mimetic peptidesSzekeres, Philip Graham January 1995 (has links)
No description available.
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Venom Peptides Lasioglossin II and Mastoparan B as Escherichia coli ATP synthase InhibitorsBello, Rafiat Ajoke 01 August 2016 (has links)
The inhibitory effects on Escherichia coli ATPase activity by two venom peptides, lasioglossin II and mastoparan B. Membrane bound F1FO ATP synthase was isolated from E. coli strain pBWU13.4/DK8 and treated with varied concentrations of lasioglossin II and mastoparan B. Lasioglossin II caused very low inhibition of ATPase activity, but the inhibition profile of mastoparan B was suggestive of an interesting biological effect. A relatively shorter total length, a smaller net positive charge, and a reduced amphipathic character of both peptides, as compared to previously tested antimicrobial peptides, may account for the limited degree of inhibition observed in the present study.
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Estudo da conformação e atividade lítica de peptídeos antimicrobianos de vespasCabrera, Marcia Perez dos Santos [UNESP] 18 August 2006 (has links) (PDF)
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cabrera_mps_dr_sjrp.pdf: 1625766 bytes, checksum: 6073fec2bef34125e9db4700102a3680 (MD5) / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) / Neste trabalho estudamos a conformação em ambientes anisotrópicos e a atividade lítica em vesículas aniônicas e zwitteriônicas de um conjunto de peptídeos biologicamente ativos, extraídos de veneno de vespas solitárias, que se caracterizam por usar seus venenos para paralisar as presas com as quais alimentam suas larvas. Esses peptídeos que são desgranuladores de mastócitos, apresentam atividade antimicrobiana e a maioria deles não é hemolítica. Possuem entre 10 e 15 resíduos, são catiônicos, com alta proporção de resíduos carregados e polares, e são lineares e helicoidais em meios miméticos de membranas. Buscamos correlacionar a atividade lítica em vesículas de diferentes composições, analisada em experimentos de fluorimetria, às mudanças conformacionais, induzidas por diferentes ambientes miméticos, monitoradas por dicroísmo circular, complementando com a análise das características físico-químicas como comprimento da cadeia, amidação do terminal-C, carga líquida, influências no macrodipolo da hélice, hidrofobicidade, momento hidrofóbico e ângulo polar. Observamos que estes peptídeos apresentam intensa atividade em membranas modelo, interagem preferencialmente com bicamadas aniônicas, e sua atividade lítica acontece de modo cooperativo tanto em vesículas aniônicas como nas zwitteriônicas. Com exceção de Anoplin, todos os peptídeos com ação antimicrobiana apresentam curvas de dose-resposta que mostram uma dependência sigmoidal com a concentração do peptídeo. Isso sugere que esses peptídeos se acumulam na superfície da vesícula até atingir uma concentração crítica, além da qual o vazamento aumenta cooperativamente. De uma forma geral os peptídeos mais eficientes como antimicrobianos, são também aqueles caracterizados pela maior eficiência em permeabilizar vesículas aniônicas do tipo PCPG 7030 e por baixas razões limite P/L. / Solitary wasps use their venoms to paralise prays to feed their larvae. A set of biologically active peptides, obtained from these venoms, have been investigated in relation to the conformational changes they undergo in anisotropic environments and their lytic activity on zwitterionic and anionic vesicles. These peptides are mast cell degranulators, present antimicrobial activities and most of them are not hemolytic. They are cationic, their chain length are 10 to 15 residues long, with high hydrophilic / hydrophobic ratio; they are linear and helical in membrane mimetic environments. We searched correlation between the lytic activity in vesicles of different compositions, monitored in fluorimetric experiments, and conformational changes, induced by varied mimetic media, monitored by circular dichroism. The results have been also correlated with peptides' physical-chemical parameters such as chain length, amidated or carboxylated C-terminal, net charge, influences on the helix macrodipole, hydrophobicity, hydrophobic moment and polar angle. We observed that these peptides present intense activity on model membranes, they interact preferentially with anionic bilayers, and their lytic activity is a cooperative process either in anionic or in zwitterionic vesicles. Exception made to Anoplin, all the other peptides that have antimicrobial activity present in their dose-response curves a sigmoidal dependence with the peptide concentration. This fact suggests that these peptides accumulate on the vesicles surface until they reach a threshold concentration, beyond which leakage increases cooperatively. As a general rule, the most efficient antimicrobial peptides are also those characterized by efficient permeabilization of anionic vesicles, namely PCPG 7030 and by small threshold P/L ratios.
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Estudo da conformação e atividade lítica de peptídeos antimicrobianos de vespas /Cabrera, Marcia Perez dos Santos. January 2006 (has links)
Orientador: João Ruggiero Neto / Banca: João Procópio de Araújo Filho / Banca: Maria Teresa Lamy / Banca: Roberto da Silva / Banca: Valmir Fadel / Resumo: Neste trabalho estudamos a conformação em ambientes anisotrópicos e a atividade lítica em vesículas aniônicas e zwitteriônicas de um conjunto de peptídeos biologicamente ativos, extraídos de veneno de vespas solitárias, que se caracterizam por usar seus venenos para paralisar as presas com as quais alimentam suas larvas. Esses peptídeos que são desgranuladores de mastócitos, apresentam atividade antimicrobiana e a maioria deles não é hemolítica. Possuem entre 10 e 15 resíduos, são catiônicos, com alta proporção de resíduos carregados e polares, e são lineares e helicoidais em meios miméticos de membranas. Buscamos correlacionar a atividade lítica em vesículas de diferentes composições, analisada em experimentos de fluorimetria, às mudanças conformacionais, induzidas por diferentes ambientes miméticos, monitoradas por dicroísmo circular, complementando com a análise das características físico-químicas como comprimento da cadeia, amidação do terminal-C, carga líquida, influências no macrodipolo da hélice, hidrofobicidade, momento hidrofóbico e ângulo polar. Observamos que estes peptídeos apresentam intensa atividade em membranas modelo, interagem preferencialmente com bicamadas aniônicas, e sua atividade lítica acontece de modo cooperativo tanto em vesículas aniônicas como nas zwitteriônicas. Com exceção de Anoplin, todos os peptídeos com ação antimicrobiana apresentam curvas de dose-resposta que mostram uma dependência sigmoidal com a concentração do peptídeo. Isso sugere que esses peptídeos se acumulam na superfície da vesícula até atingir uma concentração crítica, além da qual o vazamento aumenta cooperativamente. De uma forma geral os peptídeos mais eficientes como antimicrobianos, são também aqueles caracterizados pela maior eficiência em permeabilizar vesículas aniônicas do tipo PCPG 7030 e por baixas razões limite P/L. / Abstract: Solitary wasps use their venoms to paralise prays to feed their larvae. A set of biologically active peptides, obtained from these venoms, have been investigated in relation to the conformational changes they undergo in anisotropic environments and their lytic activity on zwitterionic and anionic vesicles. These peptides are mast cell degranulators, present antimicrobial activities and most of them are not hemolytic. They are cationic, their chain length are 10 to 15 residues long, with high hydrophilic / hydrophobic ratio; they are linear and helical in membrane mimetic environments. We searched correlation between the lytic activity in vesicles of different compositions, monitored in fluorimetric experiments, and conformational changes, induced by varied mimetic media, monitored by circular dichroism. The results have been also correlated with peptides' physical-chemical parameters such as chain length, amidated or carboxylated C-terminal, net charge, influences on the helix macrodipole, hydrophobicity, hydrophobic moment and polar angle. We observed that these peptides present intense activity on model membranes, they interact preferentially with anionic bilayers, and their lytic activity is a cooperative process either in anionic or in zwitterionic vesicles. Exception made to Anoplin, all the other peptides that have antimicrobial activity present in their dose-response curves a sigmoidal dependence with the peptide concentration. This fact suggests that these peptides accumulate on the vesicles surface until they reach a threshold concentration, beyond which leakage increases cooperatively. As a general rule, the most efficient antimicrobial peptides are also those characterized by efficient permeabilization of anionic vesicles, namely PCPG 7030 and by small threshold P/L ratios. / Doutor
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