Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/37221
Title: Development of an NOE driven method for obtaining robust and reliable models of large protein complexes
Authors: Bruton, Shaun
Supervisors: Carr, Mark
Award date: 18-Jun-2015
Presented at: University of Leicester
Abstract: The majority of proteins interact with other proteins/nucleic acids to form functional complexes that are essential to the proteins cellular role. Solving the structures of these complexes is vital for a full understanding of a proteins function. However, many protein complexes have resisted attempts of structure determination by established methods, making modelling based on experimental data and known structures of individual proteins an attractive alternative. The work presented here describes the in silico testing, experimental validation and application of a technique that uses HN-CH3 NOEs to determine sequence-specific 13C/1H NMR assignments for side-chain methyl groups in proteins, which are generally abundant at protein-protein interfaces. The approach developed relies on the preparation of residually protonated protein samples, avoiding limitations imposed by the molecular weight of larger complexes. Using this approach it was possible to obtain comprehensive assignments for the methyl groups of IL-1β (17 kDa) both in the free form and in complex with a potential therapeutic Fab antibody fragment (a complex of 65 kDa). It was shown that these assignments could be used to identify a number of backbone amide to side chain methyl NOEs across the protein-protein interface. These NOEs provided a significant number of 1H-1H distance restraints that made a substantial difference to the accuracy and reliability of docked structures obtained for the IL-1β/Fab complex by restraint driven docking. This was confirmed by comparison to a crystal structure determined for the complex. The developed approach is both conceptually and experimentally straight-forward and is expected to be generally applicable to a wide range of protein complexes up to a molecular weight of approximately 100 kDa. The use of a homology model as the starting structure for the Fab fragment also demonstrates that this technique is tolerant of some differences in the starting and final structures.
Links: http://hdl.handle.net/2381/37221
Type: Thesis
Level: Doctoral
Qualification: PhD
Rights: Copyright © the author. All rights reserved.
Appears in Collections:Theses, Dept. of Biochemistry
Leicester Theses

Files in This Item:
File Description SizeFormat 
2015_BRUTON_S_PhD.pdf8.05 MBAdobe PDFView/Open


Items in LRA are protected by copyright, with all rights reserved, unless otherwise indicated.