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dc.contributor.advisorZíková, Alena
dc.contributor.authorVáchová, Hana
dc.date.accessioned2021-12-06T14:19:29Z
dc.date.available2021-12-06T14:19:29Z
dc.date.issued2015
dc.date.submitted2015-04-24
dc.identifier.urihttps://dspace.jcu.cz/handle/20.500.14390/24797
dc.format47
dc.format47
dc.language.isocze
dc.publisherJihočeská univerzitacze
dc.rightsBez omezení
dc.subjectT. bruceieng
dc.subjectRNAieng
dc.subjectFoF1 ATPase/ATP synthaseeng
dc.titleFunctional analysis of novel F<sub>1</sub>-ATPase subunit in <i>Trypanosoma brucei</i>cze
dc.title.alternativeFunctional analysis of novel F<sub>1</sub>-ATPase subunit in <i>Trypanosoma brucei</i>eng
dc.typediplomová prácecze
dc.identifier.stag37502
dc.description.abstract-translatedAlthough F1-ATPase is extremely conserved among organisms, a putative subunit p18 was identified in Trypanosoma brucei F1-ATPase complex. To explore its function in the procylic, bloodstream and dyskinetoplastic trypanosomes, three different RNAi cell lines were created. Upon p18 silencing the F1-moiety structural integrity was impaired suggesting that p18 is indeed a bona fide subunit of this complex. Since F1-ATPase is crucial for the bloodstream form survival, its potential inhibitor from the 4-oxopiperidine-3,5-dicarboxylates class (JK-11) was examined. JK-11 inhibited growth of the bloodstream trypanosomes, decreased mitochondrial membrane potential and reduced ATPase and ATP synthase activity in mitochondrial lysates. Our results suggest that JK-11 may act on FoF1-ATP synthase/ATPase and its inhibition may contribute to the cytotoxicity of this drug.eng
dc.date.accepted2015-05-27
dc.description.departmentPřírodovědecká fakultacze
dc.thesis.degree-disciplineExperimentální biologie - specializace Buněčná a vývojová biologiecze
dc.thesis.degree-grantorJihočeská univerzita. Přírodovědecká fakultacze
dc.thesis.degree-nameMgr.
dc.thesis.degree-programBiologiecze
dc.description.gradeDokončená práce s úspěšnou obhajoboucze
dc.contributor.refereeHoráková, Eva
dc.contributor.refereeVerner, Zdeněk


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