Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680932
Title: Electron microscopy of macromolecular complexes, and their interactions with membranes
Author: Thompson, Rebecca Faith
ISNI:       0000 0004 5917 8911
Awarding Body: University of Leeds
Current Institution: University of Leeds
Date of Award: 2015
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Abstract:
Over the last ~4 years, cryo-electron microscopy (EM) has undergone a ‘revolution’, thanks to advances in microscope hardware, such as direct electron detectors, and image processing algorithms. This has improved the quality of data that can be obtained using cryo-EM, and so a diverse range of biological problems can now be effectively tackled using this technique. Here, two biological systems are examined using different cryo-EM imaging modalities. A large number of human diseases are associated with the formation of amyloid fibrils. Amyloid-membrane interactions may play a key role in amyloid mediated cytotoxicity. In Chapter Three, a combination of liposome dye release assays and cryo-EM is used to investigate the effect of amyloid fibrils on membranes of varying compositions. Solution conditions such as pH, alongside lipid composition, were found to have a profound effect on the propensity of β-2-microglobulin (β2m) amyloid fibrils to perturb membranes. In Chapter Four, subcellular fractionation and cryo-EM and tomography were used to further probe the nature of interactions between β2m amyloid fibrils and cellular membranes. Cryo-electron tomography was used to reveal 3D detail of unique interactions at molecular resolution. In Chapter Five, structural properties of the Leviviridae family of bacteriophages, a model family of spherical viruses, were investigated using cryo-EM. The structure of Qβ bacteriophage at 4.2 Å is presented. Using this electron density map, an existing X-ray crystal structure is refined to yield a better quality model of the Qβ capsid. Asymmetric reconstructions were used to generate insight into genome organisation and capsid assembly. This work demonstrates the utility of cryo-EM as a flexible technique to tackle a broad range of research questions by providing structural information at different resolutions.
Supervisor: Ranson, Neil A. ; Hewitt, Eric W. ; Radford, Sheena E. Sponsor: Wellcome Trust
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.680932  DOI: Not available
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