Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.600257
Title: Development of polypyridine metal-dependent switches as artificial regulation sites
Author: Oheix, Emmanuel
ISNI:       0000 0004 5350 4544
Awarding Body: University of Birmingham
Current Institution: University of Birmingham
Date of Award: 2014
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Abstract:
This thesis describes the design, preparation and study of synthetic peptides dimerised with polypyridine linkers. Their conformational transitions, which result from the coordination of metal-ions, are proposed to trigger the orientation of their peptide substituents, thus allowing for the design of conjugates incorporating artificial regulation sites. To test this hypothesis, different polypyridine linkers were designed, such that the substituents orientation is either dependent or independent of the polypyridine conformations. The approach developed herein includes a detailed conformational study of low-molecular weight species (model conjugates) and the preparation of conjugates mimicking a natural protein, for which dimerisation is essential for its bioactivity. For the latter conjugates, which are based on the GCN4 transcription factor, the influence of metal addition on sequence-specific DNA binding was tested using a combination of spectroscopic and electrophoretic techniques. The results presented herein indicate that metal addition can influence the interaction of the polypyridine peptide conjugates with DNA, depending on the peptides and linkers design, and that this can be partly attributed to a conformational transition of the polypyridine linker. As an extension, the potential of these conjugates as sequence-specific DNA sensors or nuclease agents was partly investigated.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.600257  DOI: Not available
Keywords: QD Chemistry
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