Newly described process in Parkinson's protein as a potential new therapy route
Flanders Institute for Biotechnology (VIB) News Oct 24, 2017
An international group of researchers led by Professor Wim Versées (VIB-VUB) has unraveled the workings of an essential mechanism in ParkinsonÂs protein LRRK2. Their study demonstrates a direct link between the proteinÂs dimerization  two copies that are bound together  and mutations that lead to ParkinsonÂs disease. This process could eventually lead to a promising therapy route.
The research findings were published in the journal Nature Communications.
The most frequent genetic causes of ParkinsonÂs disease are mutations in the gene responsible for controlling the production of protein LRRK2, which includes two enzymes: a kinase and a GTPase. Because this kinase is at the root of neuronal problems, kinase inhibitors have already been clinically tested. However, these inhibitors eventually cause lung and kidney problems, making it imperative for scientists to seek alternative solutions.
In close collaboration with Prof. Arjan Kortholt (University of Groningen), the team of Prof. Wim Versées (VIB-VUB) sought a better understanding of LRRK2Âs complex structure. It is already known that the kinase portion of the protein is active in the proteinÂs Âdimeric or Âdouble state, which involves two identical copies of the protein bound together. Using this information as a starting point, the team investigated how this binding is established. To do so, the scientists observed similar proteins occurring in certain bacteria.
Prof. Wim Versées (VIB-VUB): ÂThe GTPase enzyme, a component of LRRK2, regulates the state of the entire protein. In doing so, it determines whether a LRRK2 protein is in its inactive Âsingle state, or its active Âdouble state. In addition, we saw a clear link between the protein dimerization and genetic mutations in ParkinsonÂs disease. As a result, this regulation process constitutes an attractive new target for future drug development.Â
Prof. Arjan Kortholt (Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen) said: ÂOur study is a milestone in the long-term scientific discussion covering the dimeric state of LRRK2 and its link with ParkinsonÂs. But although this is a significant step forward, it will be quite some time before we understand all the details enough to manipulate the process.Â
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The research findings were published in the journal Nature Communications.
The most frequent genetic causes of ParkinsonÂs disease are mutations in the gene responsible for controlling the production of protein LRRK2, which includes two enzymes: a kinase and a GTPase. Because this kinase is at the root of neuronal problems, kinase inhibitors have already been clinically tested. However, these inhibitors eventually cause lung and kidney problems, making it imperative for scientists to seek alternative solutions.
In close collaboration with Prof. Arjan Kortholt (University of Groningen), the team of Prof. Wim Versées (VIB-VUB) sought a better understanding of LRRK2Âs complex structure. It is already known that the kinase portion of the protein is active in the proteinÂs Âdimeric or Âdouble state, which involves two identical copies of the protein bound together. Using this information as a starting point, the team investigated how this binding is established. To do so, the scientists observed similar proteins occurring in certain bacteria.
Prof. Wim Versées (VIB-VUB): ÂThe GTPase enzyme, a component of LRRK2, regulates the state of the entire protein. In doing so, it determines whether a LRRK2 protein is in its inactive Âsingle state, or its active Âdouble state. In addition, we saw a clear link between the protein dimerization and genetic mutations in ParkinsonÂs disease. As a result, this regulation process constitutes an attractive new target for future drug development.Â
Prof. Arjan Kortholt (Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen) said: ÂOur study is a milestone in the long-term scientific discussion covering the dimeric state of LRRK2 and its link with ParkinsonÂs. But although this is a significant step forward, it will be quite some time before we understand all the details enough to manipulate the process.Â
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