MRC DTP 4 Year PhD Programme: Prediction of protein specificity determining sites from population genetics
Prof G J Barton
Dr U Zachariae
No more applications being accepted
Competition Funded PhD Project (European/UK Students Only)
This project is part of our exciting and challenging University of Dundee 4-year MRC DTP Programme in Quantitative and Interdisciplinary approaches to biomedical science. This PhD programme brings together leading experts from the School of Life Sciences (SLS), the School of Medicine (SoM) and the School of Science and Engineering (SSE) to train the next generation of scientists at the forefront of international science. Further information on the programme structure and training can be found at https://www.dundee.ac.uk/study/pg/phds/dtp/mrc-dtp/
Our research has focused for more than 20 years on developing effective computational methods to predict the function, structure and specificity of proteins from the amino acid sequence. This experience is encapsulated in widely used software tools which include the Jalview (www.jalview.org) sequence analysis workbench that has over 70,000 regular users world-wide and JPred (www.compbio.dundee.ac.uk/jpred) which performs up to 500,000 predictions of secondary structure and other features from the amino acid sequence for scientists in laboratories in the UK and internationally. Together, Jalview and JPred have accumulated over 7,000 citations to the papers that describe them.
The rapid advances in DNA sequencing technology over recent years have stimulated the large-scale sequencing of populations of single species. There is now publically available data on variation in over 200,000 human individuals, human cancers, bacterial strains, major food crops (e.g. wheat and barley) and animals (e.g. cow). While most effort to date has focused on exploiting these data to identify variants involved in genetic disease, the variation data provides a completely new resource to inform details of protein structure, function and interactions within a species. Recent work from our group (MacGowan et al, 2017) has demonstrated that variation data can identify key residues important in protein-ligand specificity and protein-protein interaction specificity in over 200 protein domain families. This Ph.D. project will build on these findings to characterise the identified sites by a variety of techniques including molecular dynamics simulations to identify which are most likely to affect molecular function. The project will focus initially on the GPCR family of transmembrane proteins since they are a large family that provides the most statistically significant signals for specificity sites and are a focus of the research of our co-supervisor Dr Ulrich Zachariae who is also an expert in MD simulation techniques.
This project will train the student in software development and advanced bioinformatics research techniques including machine learning noSQL technology and statistics. On completion of the Ph.D. the student will be well prepared for a research career in bioinformatics, but also have excellent transferrable skills appropriate to careers in Big Data analytics or software engineering.
Stuart A MacGowan, Fábio Madeira, Thiago Britto Borges, Melanie S Schmittner, Christian Cole, and Geoffrey J Barton, (2017), “Human Missense Variation is Constrained by Domain Structure and Highlights Functional and Pathogenic Residues”, bioRxiv preprint, https://doi.org/10.1101/127050