Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.765836
Title: Peptide based biomaterials via thiol-ene chemistry
Author: Colak, Burcu
ISNI:       0000 0004 7652 3465
Awarding Body: Queen Mary University of London
Current Institution: Queen Mary, University of London
Date of Award: 2016
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Abstract:
Thiol-ene radical coupling is increasingly used for the biofunctionalisation of biomaterials and the formation of 3D hydrogels enabling cell encapsulation. Indeed, thiol-ene chemistry presents interesting features that are particularly attractive for platforms requiring specific reactions of peptides or proteins, in particular in situ, during cell culture or encapsulation: thiol-ene coupling occurs specifically between a thiol (from cysteine residues for example) and a non-activated alkene (unlike Michael addition); it is relatively tolerant to the presence of oxygen; it can be triggered by light, to trigger dynamic systems or for patterning. Despite such interest, little is known about the factors impacting thiol-ene chemistry in situ, under biologically relevant conditions. Here we explore some of the molecular parameters controlling photo-initiated thiol-ene coupling chemistry with a series of alkenes and thiols, including peptides, in buffered conditions. 1H NMR spectroscopy and HPLC were used to quantify the efficiency of couplings and the impact of the intensity of UV exposure, pH of the buffer, as well as the molecular structure and local microenvironment close to alkenes and thiols to be coupled. Our studies demonstrate that molecular design should be carefully selected in order to achieve high biofunctionalisation levels in biomaterials with peptides.
Supervisor: Not available Sponsor: Queen Mary University of London
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.765836  DOI: Not available
Keywords: thiol-ene chemistry ; Biomaterials
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