The DNA-damage response (DDR) is underpinned by a complex set of signalling pathways involving interactions that are often regulated by post-translation modifications (PTMs). In most cases the physiological effects of these modifications are unknown but it has become clear that many act as molecular ‘switches', signalling the spatially and temporally appropriate of protein assemblies. Of the many known PTMs, phosphorylation is arguably the most important and abundant and we now know of several proteins and domains https://www.findaphd.com/ t are able to specifically ‘read' phosphorylated motif signatures in target proteins. Nonetheless, the range of interactions regulated in this way remains frustratingly unclea
This project seeks to address the generic problem of how to identify and match individual phosphorylation events to functional interactions that may be rather transient in nature, initially in the specific context the DDR. This will require a highly multi-disciplinary approach combining structural, chemical and synthetic https://www.findaphd.com/test phospho-interactome of a key DDR signalling component, Nbs1. The focus will be to generate engineered Nbs1 variants that are able to trap interacting phospho-proteins allowing more robust identification than has previously been possible, thus expanding our systems-level understanding of the intricacies of DDR signalling pathways and networks. https://www.findaphd.com/test
Applicants should have a strong background in biochemistry, and ideally a background in molecular biology and/or chemistry. They should have a commitment to research in biomedicine and hold or realistically expect to obtain at least an Upper Second Class Honours Degree in biochemistry.