Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.768760
Title: Structural and biochemical characterisation of p14ARF-E3 ubiquitin ligase complexes
Author: Kowalczyk, Dominika
ISNI:       0000 0004 7655 3277
Awarding Body: University of Glasgow
Current Institution: University of Glasgow
Date of Award: 2019
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Abstract:
Post-translational modifications are a common mechanism in defining proteins role, fate and engagement in different intracellular processes. One of such modifications is ubiquitination - attachment of a small ubiquitin polypeptide to the target's lysine residue. This process involves a complex enzymatic cascade, consisting of three enzymes - E1, E2 and E3. As a result, ubiquitin is activated, conjugated and ligated to the target in a well-controlled but poorly understood manner. Ubiquitination can designate proteins for proteasomal degradation, endocytosis or alter their interaction with other partners. Any disorganisation and misregulation of that process can lead to severe disruption of cellular processes, resulting in the development of serious diseases, such as cancer or neurodegenerative disorders. MDM2 is a RING-E3 ubiquitin ligase, mainly known for its ability to ubiquitinate tumour suppressor p53 and is overexpressed in different types of cancer. MDM2 can act either as a homodimer or a heterodimer, when it's bound with its homolog - MDM4. Interestingly, despite the high sequence homology, the two proteins behave differently, depending on the dimerisation state. HUWE1 is a HECT-E3 ubiquitin ligase, which has been shown to influence the activity of a range of pro- and anti-apoptotic proteins, such as p53, MCL1 and c-MYC. Both MDM2 and HUWE1 have been reported to be inhibited by p14ARF protein, which has a prominent effect on cell survival and homeostasis. This thesis presents my work on deciphering how p14ARF influences the activity of MDM2 and HUWE1. I have focused my work on recombinant proteins grown in bacterial expression system, which were further analysed with an implementation of a range of biochemical and structural techniques. Defining an exact mechanism of p14ARF-driven inhibition of MDM2 and HUWE1 could provide long awaited knowledge, relevant for the design of new anti-cancer therapeutics.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.768760  DOI:
Keywords: QH301 Biology
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