Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.638480
Title: Novel approaches to target infectious diseases : the utility of Auger electrons and scFvs for imaging and control
Author: Rathje, Claudia Cattoni
ISNI:       0000 0004 5362 1900
Awarding Body: University of Kent
Current Institution: University of Kent
Date of Award: 2014
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Please try the link below.
Access from Institution:
Abstract:
With an increasing number of infectious agents resistant to one or more existing antibiotics, there is a global requirement for new therapeutics. One possible method for treatment of infectious diseases proposed in this study is the adaptation of a technique developed for cancer treatment, targeted radionuclide therapy, with particular interest in Auger electron radiation. Auger electrons are short range and low energy particles emitted from a range of radioactive isotopes. As a targeting agent, the antimicrobial peptide fragment UBI 29-41 was used. Antimicrobial peptides have a broad range of target microorganisms, ideal for toxicological studies of Auger electrons. Here, the baseline toxicity of UBI 29-41 was established in a range of model organisms. This enabled the analysis of the toxic effect of Auger electron emitting radio-nuclides using the isotope125I. Although no direct toxic effect was observed with this particular isotope, the labelling allows easy replacement with more potent isotopes. To further develop the targeting agent a lipoarabinomannan (LAM) specific single-chain variable fragment (scFv) was developed. LAM is a glycolipid and virulence factor associated with M. tuberculosis, the primary cause of tuberculosis in humans. By isolating the variable domains of a LAM specific monoclonal antibody, linked via a poly-glycine linker, the scFv was assembled in silico. The nucleotide sequence was optimised for and transfected into a Pichia pink expression system. Expression was successful with a ~27kDa product being secreted. The novel anti-LAM scFv generated in this study combined with the potential toxic effects of Auger electrons could provide a new avenue for the treatment and diagnosis of tuberculosis.
Supervisor: Lloyd, Dan Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.638480  DOI: Not available
Keywords: QP517 Biochemistry
Share: