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91桃色 Lab Tapped for Research into Preventing Parkinson鈥檚 Disease and Related Dementias

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Matt Meyer

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3D illustration of the brain

For the first time, a researcher in Colorado has received a Stanley Fahn Junior Faculty Award from the Parkinson鈥檚 Foundation to further academic study around the chronic neurodegenerative disorder for which there is no known cure.

Working out of the 91桃色鈥檚 , Assistant Professor of Molecular and Cellular Biophysics and his lab are developing and testing potential treatments for Parkinson鈥檚 disease (PD), which attacks the central nervous system of those affected and kills cells controlling motor function.

The $300,000 grants are awarded each year to only three researchers in North America. Kumar鈥檚 grant will help fund a study on the use of foldamers as potential drugs to treat Parkinson's disease.

Beyond the award, the foundation organizes an annual summit in Washington, D.C. for several days to honor the awardees and develop collaborations between academics and pharmaceutical companies. Kumar is invited to attend as the summit works to build understanding and better therapeutics for PD and related dementias. The foundation also reviews the research and offers feedback, something Kumar says has been valuable in the research.
鈥淭hey see a real potential in it,鈥 Kumar says. 鈥淭he award will be extremely helpful in continuing this work and the reviews for it were really nice.鈥
Graphic illustrating Parkinson's

Simply put, one of the key components of PD is clumping of a protein called a-Synuclein (aS) around neurons in the central nervous system. As the proteins build up or 鈥渁ggregate,鈥 dopamine production is slowly whittled down as cell death occurs around the brain. The drop in dopamine causes irregular brain activity, leading to the visible symptoms of PD like tremors, impaired motor function, rigidity and loss of balance. PD often develops into dementia.

On a basic level, Kumar鈥檚 lab has developed what are called 鈥渘ovel scaffolds,鈥 also known as synthetic protein mimetics or foldamers, to interrupt the buildup of aS, and thereby preserve motor function and cells in the central nervous system. Kumar says that other researchers have used peptides鈥攃hains of amino acids鈥攖o try to accomplish the same task, but the pharmaceutical properties of peptides are such that they struggle to cross the blood-brain barrier. Fully synthetic proteins have been more fruitful and, so far, there has been remarkable success in limiting the progression of PD on mice. The lab has even filed for patents related to the work.

鈥淧eptides are often chewed up by the machinery in our bodies,鈥 Kumar says. 鈥淭hese molecules don鈥檛 get chewed up and they mimic the structures of those proteins. In a person with Parkinson鈥檚, a protein will come along and bind, then another and another. Our molecules stop that. It looks like the same protein and sort of tricks the body, so it won鈥檛 keep on building clumps.鈥

More detailed information on the work can be found and , in a pair of articles in Nature Communications.

Stacia Fritz, an undergraduate researcher in Kumar鈥檚 lab, was also awarded a fellowship by the Parkinson's Foundation to carry out research in the summer. In the past, Courtney Donnelly, another undergraduate student in the lab, also received a grant to further the work.

The project includes a broad set of interdisciplinary units, encompassing NSM and the , the departments of chemistry, biology and biophysics, as well as the (KIHA).

Although it鈥檚 still relatively early in the process, Kumar says there鈥檚 potential to apply these scaffolds to other neurodegenerative diseases like amyotrophic lateral sclerosis (ALS) and even some cancers.

鈥淭here鈥檚 some really cool data and a lot of opportunity,鈥 he says.

Kumar was also quick to point out that the students working in his lab are not just graduate-level students, but also undergraduates who served as authors in different parts of the work.

鈥淲e鈥檝e been able to incorporate the work of a lot of students at different levels and that鈥檚 reflected in the authors on these papers,鈥 Kumar says. 鈥淲e work really hard, but it鈥檚 a collaborative environment.鈥