Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.745272
Title: In-silico guided prediction of allosteric sites on proteins : application to cyclin-dependent kinase 2
Author: Greener, Joe
ISNI:       0000 0004 7232 6958
Awarding Body: Imperial College London
Current Institution: Imperial College London
Date of Award: 2018
Availability of Full Text:
Access from EThOS:
Access from Institution:
Abstract:
Allostery is the functional change at one site on a protein caused by a change at a distant site. Despite being discovered more than 50 years ago allostery has remained a mystery, and there is no unified scheme to understand and predict it. In order for the the benefits of allostery to be taken advantage of, both for basic understanding of proteins and to develop new classes of drugs, computational methods to predict allosteric sites on proteins need to be developed and validated. This thesis introduces two computational methods to predict allosteric sites on proteins and describes experiments to validate a predicted allosteric site. The concepts of allostery, allosteric prediction, the protein structural ensemble and protein kinases are explained. AlloPred, which uses perturbation of normal modes alongside pocket descriptors in a machine learning approach to predict allosteric pockets, is introduced. AlloPred shows comparable and complementary performance to two existing methods. The AlloPred web server allows visualisation and analysis of predictions. ExProSE (Exploration of Protein Structural Ensembles), a distance geometry-based method that generates an ensemble of protein structures from two input structures, is described. ExProSE is able to access conformational changes inaccessible to classical molecular dynamics. By adding additional constraints to the method, the effect of allosteric modulators can be predicted. ExProSE is shown to be effective at allosteric site prediction in a systematic comparison of methods. A predicted allosteric pocket on cyclin-dependent kinase 2, a medically-important protein kinase involved in cell cycle regulation, is explored experimentally. Selected compounds from virtual screening are tested in two assays, though no conclusive results are obtained. The development and adoption of methods such as those presented here is essential or the long-preached potential of allostery will remain elusive.
Supervisor: Sternberg, Michael Sponsor: Biotechnology and Biological Sciences Research Council
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.745272  DOI:
Share: