Every thought, movement, and memory depends on AMPA receptors—tiny protein gateways on brain cells that handle the vast majority of signals passing between neurons. This project investigates how neurons manage the extraordinary task of placing these receptors in exactly the right spots at exactly the right times, and how they rapidly adjust their numbers and positions in response to activity. The problem is fundamental: we know AMPA receptors must be precisely positioned for the brain to work, but the molecular machinery that transports, anchors, and removes them remains poorly understood. Without this knowledge, we cannot fully grasp how healthy brains process information, nor what goes wrong when receptor trafficking fails—as it does in conditions like epilepsy, stroke, and neurodegenerative diseases. This is fundamental science. It will not produce a drug or device tomorrow. But understanding the basic rules of receptor trafficking has historically opened unexpected doors: similar work on synaptic proteins laid groundwork for drugs that treat depression and chronic pain. A clearer picture of how neurons control receptor location could eventually reveal new targets for therapies that restore normal signalling in diseased brains.
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Glutamate is a molecule in the brain that transfers messages from one neurone to the next. In the receiving neurone, glutamate binds to proteins called receptors that activate that neurone which, in turn, often stimulates it to release glutamate itself to activate the next neurone in the chain. We are particularly interested in the glutamate receptor subtype called AMPA receptors (AMPARs). Information passing through AMPARs represents the vast majority of information flow in the brain. To function correctly, AMPARs need to be precisely located on the surface of the neurone. The focus of our work is how neurones achieve the remarkable feat of getting the AMPARs to the right place at the right time. In addition, the number and location of AMPARs can be rapidly changed. It has been discovered that there are proteins that direct and anchor AMPARs; they determine the level and location of AMPAR expression and they connect to specific signalling pathways inside the neurone. This project aims to provide a more complete picture of how AMPARs are transported (trafficked) around the neurone and define the specific roles of interacting proteins. We shall use a combination of methods that takes full advantage of the technological advances made over the last few years to elucidate the principles that govern the turnover and surface expression of AMPARs. To do this we will look at what happens in both resting, unstimulated neurones and also in neurones that have been stimulated with physiologically relevant stimuli. We will use new microscopes and special fluorescent protein labels that allow us to actually see AMPARs moving in the cell and how this is changed by different conditions. We will then use biochemical methods to work out what proteins are involved in orchestrating these movements and what happens when we prevent them from working properly. The public can access neuroscience research in the University of Bristol via Bristol Neuroscience (BN). There is an extensive website that allows the public to gain access to the research going on in our labs. BN is also active in arranging events to increase public understanding of science. Via BN and the widening participation scheme the PI gives talks about ?how the brain works? to A-level students in schools.
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