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dc.contributor.advisorWhite, Malcolm F.
dc.contributor.advisorPenedo, Carlos
dc.contributor.authorFritzen, Remi
dc.coverage.spatial261en_US
dc.date.accessioned2023-04-18T08:16:42Z
dc.date.available2023-04-18T08:16:42Z
dc.date.issued2021-11-30
dc.identifier.urihttps://hdl.handle.net/10023/27415
dc.description.abstractDNA, or deoxyribonucleic acid, contains the molecular blueprint of organisms. Although, very stable, DNA can be damaged by genotoxic agents such as UV-light, reactive oxygen species or chemotherapeutic drugs, amongs others. Organisms have evolved several biological pathways to repair different types of damage and nucleotide excision repair (NER) is one of them. NER repairs mainly lesions inducing structural distortion of the double helix. Briefly, the lesion is detected, unwinding takes place to create a 30 nucleotides long bubble, the damage-containing single strand is then excised; using the opposite strand as a template, the DNA is resynthesized and ligated. Nucleotide Excision Repair is a non-mutagenic repair system. Single-strand DNA binding proteins (SSB) are involved in NER and many other pathways. Their role is to coat and protect the ssDNA from degradation and re-hybridisation. Here, we studied SSBs from Saccharolobus solfataricus and Sulfolobus acidocaldarius as well as a chimeric protein containing DNA binding domains from both organisms. We showed that the chimeric protein had better resistance to extreme conditions of temperature, ionic strength or acidic pH. We also proved that our chimeric SSB can be used as a tool to image single strand DNA or RNA using super resolution microscopy. The first step of NER is damage recognition by XPC. We studied XPC binding to a DNA substrate and showed the possibility of two XPC binding to a damage whilst demonstrating that the presence of a nick on the DNA backbone does not constitute a substrate for XPC. Furthermore, we used single molecule FRET technique to show that XPC could bind a three nucleotides bubble in two different modes, showing a strong preference for one of these binding modes. The second step is the unwinding by the XPD helicase, we studied the impact of the purine/pyrimidine composition on the unwinding activity and investigated a possible damage sensor role of XPD, using Archaean models. To complete our work, we demonstrated a cooperative effect on the distortion of the repair bubble of XPA and RPA.en_US
dc.description.sponsorship"This work was supported by a Wellcome Trust ISSF grant (number: 20481/Z/12/Z) as well as a BBSRC grant (number: BBR015570/1)." --Fundingen
dc.language.isoenen_US
dc.publisherUniversity of St Andrews
dc.relationShedding Light on DNA-Protein Interactions involved in the Nucleotide Excision Repair pathway - Chapter III - SSBs (thesis data) Fritzen, R., University of St Andrews, 4 Feb 2025. DOI: https://doi.org/10.17630/963932fc-cc3e-4b69-b92d-58108e138657en
dc.relationColizzi, F., Perez-Gonzalez, C., Fritzen, R., Levy, Y., White, M. F., Penedo, J. C., & Bussi, G. (2019). Asymmetric base-pair opening drives helicase unwinding dynamics. Proceedings of the National Academy of Sciences of the United States of America, 116(45), 22471-22477. https://doi.org/10.1073/pnas.1901086116 [http://hdl.handle.net/10023/18714 : Open Access version]en
dc.relation.urihttps://doi.org/10.17630/963932fc-cc3e-4b69-b92d-58108e138657
dc.relation.urihttp://hdl.handle.net/10023/18714
dc.subjectXPAen_US
dc.subjectRPAen_US
dc.subjectTFIIHen_US
dc.subjectXPDen_US
dc.subjectNucleotide excision repairen_US
dc.subjectSingle-strand binding proteinsen_US
dc.subjectXPCen_US
dc.subjectSingle molecule microscopyen_US
dc.subject.lccQH467.F8
dc.subject.lcshDNA repairen
dc.titleShedding light on DNA-protein interactions involved in the nucleotide excision repair pathwayen_US
dc.typeThesisen_US
dc.contributor.sponsorWellcome Trust. Institutional Strategic Support Fund (ISSF)en_US
dc.contributor.sponsorBiotechnology and Biological Sciences Research Council (BBSRC)en_US
dc.type.qualificationlevelDoctoralen_US
dc.type.qualificationnamePhD Doctor of Philosophyen_US
dc.publisher.institutionThe University of St Andrewsen_US
dc.rights.embargodate2025-02-04en
dc.rights.embargodateThesis restricted in accordance with University regulations. Restricted until 4th February 2025en
dc.identifier.doihttps://doi.org/10.17630/sta/404
dc.identifier.grantnumber204821/Z/12/Zen_US
dc.identifier.grantnumberBB/R015570/1en_US


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