• Login
• Admin

Mayer, Matthias (2023) Analysis of substrate selectivity determinants in Ubiquitin Specific Proteases 11 and 15. PhD thesis, University of Nottingham.

PDF (Thesis - as examined) - Repository staff only until 21 December 2024. Subsequently available to Repository staff only - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader Available under Licence Creative Commons Attribution. Download (5MB)

Abstract

Ubiquitin Specific Proteases (USPs) have long been studied for various physiological effects, being involved in many cellular processes as well as many different cancers. The variety of the USP family as well as the large variation in substrates has made them the subject of drug trials in the past. However, as one USP can target many different substrate in cells, more work should be done to analyse what directs this substrate specificity.

This investigation aims to elucidate which amino acids direct the substrate specificity of USPs.

USP11, a poor cleaver of linear diubiquitin, was analysed using sequence analysis and a previous structure to identify amino acids which affect substrate specific activity. This aspartic acid residue proximal to the catalytic histidine (USP11D886) was shown to affect cleavage of linear diubiquitin, with a glycine in this position drastically increasing cleavage rates. The reverse mutation in USP15 (USP15G860D) demonstrated complementary results. However, two binding forms leads to a complex analysis of the interaction through isothermal titration calorimetry (ITC) and microscale thermophoresis (MST). An X-ray crystallography derived structure with novel protein tags to aid crystallographic study shows evidence of multiple binding sites between USP11 and diubiquitin. This showcases a promising target for substrate specific activity, with the proximal aspartic acid/glycine residue being a druggable target for specific interactions.

Item Type:	Thesis (University of Nottingham only) (PhD)
Supervisors:	Dreveny, Ingrid
Keywords:	Ubiquitin Specific Proteases, Ubiquitin, enzymes
Subjects:	Q Science > QP Physiology > QP501 Animal biochemistry R Medicine > RM Therapeutics. Pharmacology
Faculties/Schools:	UK Campuses > Faculty of Science > School of Pharmacy
Item ID:	76574
Depositing User:	Mayer, Matthias
Date Deposited:	16 Jan 2024 10:43
Last Modified:	16 Jan 2024 10:43
URI:	https://eprints.nottingham.ac.uk/id/eprint/76574

Actions (Archive Staff Only)

Edit View