The questions we address deal with the molecular mechanisms that underlie signalling between cells, and cellular responses to stress. These processes are implicated in multiple human diseases including cancer, neurodegeneration, inflammation and infection so, although we mostly do discovery science, our work has wide potential medical relevance.
Our particular focus is the rhomboid-like superfamily of membrane proteins. We were the first to discover rhomboids, and we proved that they were novel intramembrane proteases, conserved across evolution, and that they controlled growth factor signalling. Since then, the rhomboids have been implicated in many biological processes including, for example, growth factor activation, neurodegeneration, mitochondrial function, host cell invasion by parasites and bacterial physiology.
More recently we have become interested in the much wider superfamily of rhomboid-like proteins, the majority of which are not proteases. We have studied a few examples and have uncovered roles in controlling the cellular fate of membrane proteins.
Our experimental approaches include genetics, cell biology, biochemistry and structural biology, mainly in mammalian cells but also with a variety of model systems including mice, Drosophila and yeast. Although our main effort is aimed at understanding fundamental biology of the rhomboid-like superfamily, we are also actively pursuing the potential medical significance of our basic discoveries.
Freeman lab
Investigating the interface between membrane proteins, the cell biology of signalling, and mechanisms of human disease
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About our PhD course
Doing a DPhil in Molecular Cell Biology in Health and Disease at the Dunn School is the best way to start your career.