Alpha-synuclein is a key player in Parkinson’s disease, dementia with Lewy bodies, multiple system atrophy, and perhaps even other neurodegenerative diseases, because it accumulates as misfolded species in the brains of the patients as they age and as disease progresses. We know that this protein exists in high amounts in the synaptic compartment, and we know from the work of many colleagues in the field that it seems to influence synaptic function by interfering with the release of synaptic vesicles...
Alpha-synuclein is a key player in Parkinson’s disease, dementia with Lewy bodies, multiple system atrophy, and perhaps even other neurodegenerative diseases, because it accumulates as misfolded species in the brains of the patients as they age and as disease progresses. We know that this protein exists in high amounts in the synaptic compartment, and we know from the work of many colleagues in the field that it seems to influence synaptic function by interfering with the release of synaptic vesicles.
So here in my talk, it’s a short talk, so we’ll not be able to cover everything we do in detail, but what I’ll try to do is to really highlight some of our most recent work where we are trying to use super resolution microscopy techniques to image alpha-synuclein in the synaptic compartment, to image its interactions with other proteins, and we think this might be relevant in the context of the biology, but also of the pathobiology of alpha-synuclein. And I will touch on a study that we did recently, where we used proteomics to find interactors, and we found that some of these dangerous interactions could be with mitochondrial proteins that should normally be going into the mitochondria, and because alpha-synuclein may be interacting with them, they are kept in the cytosol and will not play their role where they should be playing in the mitochondria and so this may compromise mitochondrial function. So in a nutshell, this is what I’ll try to do in my presentation.