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間眅埶AV researchers developing drug that could halt progression of Parkinson's disease

December 02, 2020
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A team of 間眅埶AV researchers developing a drug design approach that could lead to new disease-modifying therapeutics for diseases such as Parkinsons have been awarded a $1 million grant from the Canadian Institutes for Health Research.

Led by professor of chemistry Andrew Bennet, the team which also includes 間眅埶AVs David Vocadlo, Rob Britton and University of Manitobas Brian Mark hopes to develop the first treatment that can alter the course of the disease and stop its progression, rather than just treating the symptoms.

Parkinsons has been linked to deficiencies in an enzyme called glucocerebrosidase, which is critical to breaking down waste products in the body into more easily metabolized components like glucose and ceramide, a type of fat. However, genetic mutations associated with this enzyme can result in an unstable structure and a loss of function that can cause damage to the body and contributes to the progression of Parkinsons disease.

The approach of Bennets team is to design small molecules that form a chemical bond to the mutated enzyme, acting as a mannequin, mimicking the enzymes natural substrate, and tricking glucocerebrosidase into folding around the small molecules like a suit. Once its job is done, the molecules break off from the tailored enzyme, allowing it to be worn by other molecules in the body and once again perform its critical role of breaking down waste.

The economic cost of Parkinsons disease alone is estimated at $14.4 billion annually in the US and its prevalence is predicted to more than double by 2040. Current therapies treat the symptoms of the disease, but do not alter the disease course. Identifying new disease-modifying therapies is a critical, unmet need. The fundamental chemical biology studies underway by this research team promises to yield key insights and tools that will enable the biotechnology sector to develop disease-modifying therapeutics for Parkinsons disease and the many other so-called lysosomal storage disorders.

AVAILABLE 間眅埶AV EXPERTS

Andrew Bennet, professor, Department of Chemistry, bennet@sfu.ca

CONTACT

Matt Kieltyka,  間眅埶AV Communications & Marketing 
236.880.2187 | matt_kieltyka@sfu.ca

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