Professor David Allsop
Professor of Neuroscience
The formation of fibrillar aggregates from a range of different proteins is a common feature of numerous different 'protein conformational' diseases. In these diseases, normally soluble proteins are deposited in the form of insoluble fibrils inside and/or outside of cells. In the systemic amyloidoses, extracellular fibrillar deposits (often called amyloid) can be found in many different tissues and organs throughout the body. Localised deposits are found in some other diseases, such as late-onset diabetes, where they are restricted to the pancreas, and some important neurodegenerative diseases, where they are often found only in the brain. Examples of the latter include Alzheimer's disease, Parkinson's disease, the prion diseases (e.g. CJD in humans), Huntington's disease, frontotemporal dementia and motor neuron disease. My research is concerned with the pathological role of these misfolded proteins, and is focussed mainly on neurodegenerative disease and late-onset (type 2) diabetes.