Parkinson’s Protein Plays Vital Marshalling Role in Healthy Brains

Summary: Researchers report alpha-synuclein helps to marshal the correct number of vesicles into the right position to release their neurotransmitters across synapses.

Source: Imperial College London.

Researchers have uncovered the normal function of a protein associated with Parkinson’s disease, giving clues about what happens when it malfunctions.

By showing how the protein – called alpha-synuclein – works in healthy patients, the study offers important clues about what may be happening when it malfunctions and people develop the disease.

While malfunctioning alpha-synuclein has long been recognised as a hallmark of Parkinson’s disease, its role in healthy brains was not properly understood until now. The new study, carried out by researchers at Imperial College London and the University of Cambridge shows that the protein plays a vital role in signalling in the brain.

The research team found that alpha-synuclein regulates the interaction between synaptic vesicles, which are small containers of neurotransmitters – the signalling chemicals of the brain. Alpha-synuclein helps to marshal the correct number of vesicles into the right position to release their neurotransmitters across junctions between nerve cells, known as synapses.

Two different regions of the protein were found to have membrane-binding properties that mean it can attach itself to vesicles and hold some of them in place, while others are released.

Significantly, the researchers also tested mutated forms of alpha-synuclein that are linked to Parkinson’s disease. These were found to interfere with the same mechanism, compromising the ability of the brain to signal between neurons. The research is published today in Nature Communications.

MACHINE LEARNING

Study co-author Dr Alfonso De Simone from the Department of Life sciences at Imperial said: “If you remove part of a machine, you need to know what it is supposed to do before you can understand what the consequences of its removal are likely to be.”

“We have had a similar situation with Parkinson’s disease; we needed to know what alpha-synuclein actually does in order to identify the right strategies to target it as a therapeutic approach to Parkinson’s.”

Giuliana Fusco, a Chemistry PhD student from the University of Cambridge who has now joined the team at Imperial, carried out the main experiments underpinning the research. She said: “It was already clear that alpha-synuclein plays some sort of role in regulating the flow of synaptic vesicles at the synapse, but our study presents the mechanism, explaining exactly how it does it.”

Image shows a-synuclein linking transporters.
Alpha-synuclein (red) acts as a bond between cellular
transporters in healthy brains NeuroscienceNews.com image is adapted from the Imperial College press release.

“Because we have shown that mutated forms of alpha-synuclein, which are associated with early onset familial forms of Parkinson’s disease, affect this process, we also now know that this is a function that may be impaired in people who carry these mutations.”

COMPROMISED ROLE

The research suggests that in some familial cases of early onset Parkinson’s disease, because alpha-synuclein malfunctions as a result of genetic alterations, the protein’s marshalling role is compromised.

One of the trademarks of Parkinson’s disease, for example, is an excess of alpha-synuclein in the brain. In such circumstances, it is possible that too much binding will take place and the flow of vesicles will be limited, preventing effective neurotransmission.

The study involved lab-based experiments in which synthetic vesicles, modelling the synaptic vesicles found the brain, were exposed to alpha-synuclein.

Using nuclear magnetic resonance spectroscopy, the researchers examined how the protein organised itself structurally in relation to the vesicles. To verify the findings, additional tests were then carried out on samples taken from the brains of rats.

About this neuroscience research article

Source: Hayley Dunning – Imperial College London
Image Source: NeuroscienceNews.com image is adapted from the Imperial College press release.
Original Research: Full open access research for “Structural Basis of Synaptic Vesicle Assembly Promoted by α-Synuclein” by Giuliana Fusco, Tillmann Pape, Amberley D. Stephens, Pierre Mahou, Ana Rita Costa, Clemens F. Kaminski, Gabriele S. Kaminski Schierle, Michele Vendruscolo, Gianluigi Veglia, Christopher M. Dobson and Alfonso De Simone in Nature Communications. Published online September 19 2016 doi:10.1038/ncomms12563

Cite This NeuroscienceNews.com Article

[cbtabs][cbtab title=”MLA”]Imperial College London “Parkinson’s Protein Plays Vital Marshalling Role in Healthy Brains.” NeuroscienceNews. NeuroscienceNews, 19 September 2016.
<https://neurosciencenews.com/parkinsons-genetics-alpha-synuclein-5072/>.[/cbtab][cbtab title=”APA”]Imperial College London (2016, September 19). Parkinson’s Protein Plays Vital Marshalling Role in Healthy Brains. NeuroscienceNew. Retrieved September 19, 2016 from https://neurosciencenews.com/parkinsons-genetics-alpha-synuclein-5072/[/cbtab][cbtab title=”Chicago”]Imperial College London “Parkinson’s Protein Plays Vital Marshalling Role in Healthy Brains.” https://neurosciencenews.com/parkinsons-genetics-alpha-synuclein-5072/ (accessed September 19, 2016).[/cbtab][/cbtabs]


Abstract

Structural Basis of Synaptic Vesicle Assembly Promoted by α-Synuclein

α-synuclein (αS) is an intrinsically disordered protein whose fibrillar aggregates are the major constituents of Lewy bodies in Parkinson’s disease. Although the specific function of αS is still unclear, a general consensus is forming that it has a key role in regulating the process of neurotransmitter release, which is associated with the mediation of synaptic vesicle interactions and assembly. Here we report the analysis of wild-type αS and two mutational variants linked to familial Parkinson’s disease to describe the structural basis of a molecular mechanism enabling αS to induce the clustering of synaptic vesicles. We provide support for this ‘double-anchor’ mechanism by rationally designing and experimentally testing a further mutational variant of αS engineered to promote stronger interactions between synaptic vesicles. Our results characterize the nature of the active conformations of αS that mediate the clustering of synaptic vesicles, and indicate their relevance in both functional and pathological contexts.

“Structural Basis of Synaptic Vesicle Assembly Promoted by α-Synuclein” by Giuliana Fusco, Tillmann Pape, Amberley D. Stephens, Pierre Mahou, Ana Rita Costa, Clemens F. Kaminski, Gabriele S. Kaminski Schierle, Michele Vendruscolo, Gianluigi Veglia, Christopher M. Dobson and Alfonso De Simone in Nature Communications. Published online September 19 2016 doi:10.1038/ncomms12563

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