An illustration of how the mitochondria-imitating lipid vesicles are damaged by the Parkinson’s protein alpha-synuclein. The light scattering shows how the membrane is destroyed even at very low, nanomolar, concentrations, where proteins do not aggregate to clumps before they bind. Illustration: Fredrik Höök
Parkinson's disease is an incurable condition in which neurons, the brain's nerve cells, gradually break down and brain functions become disrupted. Symptoms can include involuntary shaking of the body, and the disease can cause great suffering. To develop drugs to slow down or stop the disease, researchers try to understand the molecular mechanisms behind how α-synuclein contributes to the degeneration of neurons.
It is known that mitochondria, the energy-producing compartments in cells, are damaged in Parkinson's disease, possibly due to ‘amyloids’ of α-synuclein. Amyloids are clumps of proteins arranged into long fibres with a well-ordered core structure, and their formation underlies many neurodegenerative disorders. Amyloids or even smaller clumps of α-synuclein may bind to and destroy mitochondrial membranes, but the precise mechanisms are still unknown.
New method reveals structural damage to mitrochondrial membranes
The new study, recently published in the journal PNAS, focuses on two different types of membrane-like vesicles. One of them is made of lipids that are often found in synaptic vesicles, the other contained lipids related to mitochondrial membranes.
The researchers found that the Parkinson’s protein would bind to both vesicle types, but only caused structural changes to the mitochondrial-like vesicles, which deformed asymmetrically and leaked their contents.
“Now we have developed a method which is sensitive enough to observe how α-synuclein interacts with individual model vesicles, which are ‘capsules’ of lipids that can be used as mimics of the membranes found in cells. In our study, we observed that α-synuclein binds to – and destroys – mitochondrial-like membranes, but there was no destruction of the membranes of synaptic-like vesicles. The damage occurs at very low, nanomolar concentration, where the protein is only present as monomers – non-aggregated proteins. Such low protein concentration has been hard to study before but the reactions we have detected now could be a crucial step in the course of the disease,” says Pernilla Wittung-Stafshede, Professor of Chemical Biology at the Department of Biology and Biological Engineering.
"Dramatic differences in how the protein affects membranes"
The new method from the researchers at Chalmers University of Technology makes it possible to study tiny quantities of biological molecules without using fluorescent markers. This is a great advantage when tracking natural reactions, since the markers often affect the reactions you want to observe, especially when working with small proteins such as α-synuclein.
“The chemical differences between the two lipids used are very small, but still we observed dramatic differences in how α-synuclein affected the different vesicles,” says Pernilla Wittung-Stafshede.
“We believe that lipid chemistry is not the only determining factor, but also that there are macroscopic differences between the two membranes – such as the dynamics and interactions between the lipids. No one has really looked closely at what happens to the membrane itself when α-synuclein binds to it, and never at these low concentrations.”
Next step: Investigate proteins with mutations and cellular membranes
The next step for the researchers is to investigate variants of the α-synuclein protein with mutations associated with Parkinson's disease, and to investigate lipid vesicles which are more similar to cellular membranes.
“We also want to perform quantitative analyses to understand, at a mechanistic level, how individual proteins gathering on the surface of the membrane can cause damage” says Fredrik Höök, Professor at the Department of Physics, who was also involved in the research.
“Our vision is to further refine the method so that we can study not only individual, small – 100 nanometres – lipid vesicles, but also track each protein one by one, even though they are only 1-2 nanometres in size. That would help us reveal how small variations in properties of lipid membranes contribute to such a different response to protein binding as we now observed.”
Text: Susanne Nilsson Lindh and Joshua Worth
Illustration: Fredrik Höök
More information on the method
- Vesicle membranes were observed by measuring light scattering and fluorescence from vesicles which were bound to a surface – and monitoring the changes when low concentrations of α-synuclein were added.
- Using high spatiotemporal resolution, protein binding and the resulting consequences on the structure of the vesicles, could be followed in real time. By means of a new theory, the structural changes in the membranes could be explained geometrically.
- The method used in the study was developed by Björn Agnarsson in Fredrik Höök's group and utilises an optical-waveguide sensor constructed with a combination of polymer and glass. The glass provides good conditions for directing light to the sensor surface, while the polymer ensures the light does not scatter and cause unwanted background signals.
- The combination of good light conduction and low background interference makes it possible to identify individual lipid vesicles and microscopically monitor their dynamics as they interact with the environment – in this case, the added protein. Sandra Rocha in Pernilla Wittung-Stafshede's group provided α-synuclein expertise, which is a complicated protein to work with.
- The research project is mainly funded by the Area of Advance for Health Engineering at Chalmers University of Technology, and scholar grants from the Knut and Alice Wallenberg Foundation. The researchers’ complementary expertise around proteins, lipid membranes, optical microscopy, theoretical analysis and sensor design from Chalmers’ clean room has been crucial for this project.
Read the full study in PNAS:
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