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Activation of the vasopressin and oxytocin receptor family: structural and mechanistic insights

La-Borde, Penelope Jane (2017)
Ph.D. thesis, University of Birmingham.

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Abstract

G-protein-coupled receptors (GPCRs) are major pharmaceutical drug targets due to their crucial role in cell signalling. The neurohypophysial peptide hormones [Arg\(^8\)] vasopressin (AVP) and oxytocin (OT) signal through a subfamily of GPCRs, comprising the AVP receptors (V\(_1\)\(_a\)R, V\(_1\)\(_b\)R and V\(_2\)R) and the OT receptor (OTR).

The aim of this work was to understand the molecular basis of receptor activation by defining exact contacts between agonist and receptor. Molecular modelling suggested that two conserved negatively-charged residues may be important for agonist binding and receptor activation. Interactions between agonists and the human AVP/OT receptors were probed using a combination of site-directed mutagenesis of the receptors and ligands incorporating modifications at specific points. The wild-type (WT) and mutant receptors were expressed in HEK 293T cells and pharmacologically characterised with respect to ligand binding, receptor activation, cell surface expression and ligand-induced internalisation when stimulated by endogenous, or modified, ligands.

Mutual exchange of functional groups revealed direct interactions between AVP/OT/[Arg\(^8\)] vasotocin (AVT; a chimera of AVP and OT) and the human AVP/OT receptors required for receptor activation. These studies advance current understanding of the molecular basis of receptor activation and have the potential to facilitate future rational drug design.

Type of Work:Ph.D. thesis.
Supervisor(s):Wheatley, Mark
School/Faculty:Colleges (2008 onwards) > College of Life & Environmental Sciences
Department:School of Biosciences
Additional Information:

Thesis is under an option D embargo until 31/07/2020.

Subjects:QD Chemistry
QH301 Biology
RM Therapeutics. Pharmacology
Institution:University of Birmingham
ID Code:7639
This unpublished thesis/dissertation is copyright of the author and/or third parties. The intellectual property rights of the author or third parties in respect of this work are as defined by The Copyright Designs and Patents Act 1988 or as modified by any successor legislation. Any use made of information contained in this thesis/dissertation must be in accordance with that legislation and must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the permission of the copyright holder.
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