Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.736482
Title: Targeting the essential interactions of the M2-1 protein of human respiratory syncytial virus (HRSV) for anti-viral drug development
Author: Dods, Rachel Linda
ISNI:       0000 0004 6500 2840
Awarding Body: University of Leeds
Current Institution: University of Leeds
Date of Award: 2017
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Thesis embargoed until 01 Mar 2023
Access from Institution:
Abstract:
Human respiratory syncytial virus (HRSV) is a non-segmented negative stranded RNA virus classified within the Mononegavirales order. HRSV is the leading cause of lower respiratory tract illness in young children and the immunocompromised, with over 250,000 annual fatalities worldwide. HRSV-mediated diseases are especially prevalent in developing countries, where no financially viable treatment exists. The M2-1 protein of HRSV represents a promising potential anti-viral target for the treatment of HRSV-mediated diseases. M2-1 is a transcription antiterminator with an essential role in viral gene expression. M2-1 binds both viral RNA and the polymerase co-factor phosphoprotein (P), and these interactions are essential for its anti-termination activity. Here, the crystal structure of M2-1 in complex with a P protein peptide was determined and used in addition to the unbound M2-1 crystal structure as a basis to identify potential anti-viral compounds. Structure based drug design (SBDD) of M2-1s interaction interface with RNA/ P produced hit compounds that were analysed through biophysical, structural and in cellulo methods including the use of a mini-genome and infectious HRSV assay. SBDD identified hit compounds that significantly inhibited the growth of HRSV. Subsequently, synthetic chemistry was used to generate libraries of molecules to establish structure-activity relationships (SAR) as well as assess their pharmacokinetic properties. Further, a novel facility that allowed assessment of fragment binders to HRSV M2-1 by X-ray crystallography was utilised to determine hit binders towards the entire M2-1 protein, including the previously targeted RNA/ P surface and allowed further rapid SAR. The work presented here represents an effective strategy to rationally design anti-viral compounds for the M2-1 protein of HRSV with potential applications for the related virus, bovine respiratory syncytial virus (BRSV).
Supervisor: Barr, John N. Sponsor: University of Leeds
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.736482  DOI: Not available
Share: