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dc.contributor.advisorFessl, Tomáš
dc.contributor.authorKruglhuber, Anna
dc.date.accessioned2026-01-06T11:54:25Z
dc.date.available2026-01-06T11:54:25Z
dc.date.issued2023
dc.date.submitted2023-08-09
dc.identifier.urihttps://dspace.jcu.cz/handle/20.500.14390/48537
dc.description.abstractAmongst bacteria, living in complex and varying communities and surroundings, rivalry for crucial resources exists. Due to the constant pressure, strategies to allow competition and communication have been developed within bacterial communities. In this respect, Contact Dependent Growth Inhibition (CDI) is often of relevance. The aim was to elucidate a newly found pathway of transport of the CDI toxins across the inner bacterial membrane via Sec translocon. Since all proteins are transported via Sec translocon in an unfolded state, and there is no obvious mechanism which would drive or facilitate this transport in the retrograde fashion, the hypothesis that the effector domain of CDI toxins evolved an anisotropic energy landscape of mechanical unfolding was constructed. That would allow the toxin to be mechanically more labile in the direction of translocation and mechanically stable in the orthogonal directions. This anisotropy would permit efficient translocation and overall thermodynamic stability at the same time. The unfolding landscape was assessed by a molecular dynamics simulation combined with umbrella sampling. Developed methodology, complemented with a rational design of "circular permutants", helped to estimate the forces required to unfold the toxins under different geometries.cze
dc.format51 p. (110 296 characters)
dc.format51 p. (110 296 characters)
dc.language.isoeng
dc.publisherJihočeská univerzitacze
dc.rightsPráce bude přístupná od 20.09.2026
dc.subjectcontact-dependent inhibition (CDI)cze
dc.subjectSecYEG transloconcze
dc.subjectmolecular dynamics simulationscze
dc.subjectCdiA toxincze
dc.subjectanisotropycze
dc.subjectmechanical unfoldingcze
dc.subjectretrograde translocation mechanismcze
dc.subjectcontact-dependent inhibition (CDI)eng
dc.subjectSecYEG transloconeng
dc.subjectmolecular dynamics simulationseng
dc.subjectCdiA toxineng
dc.subjectanisotropyeng
dc.subjectmechanical unfoldingeng
dc.subjectretrograde translocation mechanismeng
dc.titleMechanism of retrograde transport in contact-dependent inhibition (CDI) toxins through the bacterial transloconcze
dc.title.alternativeMechanism of retrograde transport in contact-dependent inhibition (CDI) toxins through the bacterial transloconeng
dc.typebakalářská prácecze
dc.identifier.stag66640
dc.description.abstract-translatedAmongst bacteria, living in complex and varying communities and surroundings, rivalry for crucial resources exists. Due to the constant pressure, strategies to allow competition and communication have been developed within bacterial communities. In this respect, Contact Dependent Growth Inhibition (CDI) is often of relevance. The aim was to elucidate a newly found pathway of transport of the CDI toxins across the inner bacterial membrane via Sec translocon. Since all proteins are transported via Sec translocon in an unfolded state, and there is no obvious mechanism which would drive or facilitate this transport in the retrograde fashion, the hypothesis that the effector domain of CDI toxins evolved an anisotropic energy landscape of mechanical unfolding was constructed. That would allow the toxin to be mechanically more labile in the direction of translocation and mechanically stable in the orthogonal directions. This anisotropy would permit efficient translocation and overall thermodynamic stability at the same time. The unfolding landscape was assessed by a molecular dynamics simulation combined with umbrella sampling. Developed methodology, complemented with a rational design of "circular permutants", helped to estimate the forces required to unfold the toxins under different geometries.eng
dc.date.accepted2023-09-20
dc.description.departmentPřírodovědecká fakultacze
dc.thesis.degree-disciplineBiological Chemistrycze
dc.thesis.degree-grantorJihočeská univerzita. Přírodovědecká fakultacze
dc.thesis.degree-nameBc.
dc.thesis.degree-programBiological Chemistrycze
dc.description.gradeDokončená práce s úspěšnou obhajoboucze
dc.contributor.refereeFranta, Zdeněk
dc.description.defence<p>Dr Štěrba welcomed the student and commission members; Prof Vácha was not present. The student presented the theoretical background of her work on the transport system the studied proteins and the used methods, followed by the experimental part and the results. The supervisor, Dr Fessl, and the opponent, Dr. Franta, presented their reviews. The student answered all the questions of the opponent and also questions from the commission members regarding future experiments, additional possible measurements, the requirement of energy for unfolding and refolding and the conditions for refolding of the transported proteins.<br /> Votes: 4x 1<br /> Final grade: 1<br /> Points:&nbsp; 145&nbsp;&nbsp; &nbsp;<br /> The commission recommends this thesis to be awarded by the head of the department.</p>cze


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