Virtually all neurodegenerative diseases are characterized by the accumulation of proteins that are thought to play a significant role in disease pathogenesis. One of the cell?s primary systems for the removal and degradation of misfolded or damaged proteins is the Ubiquitin Proteasome System (UPS). However, numerous studies have shown significant impairment of the UPS in essentially all of these neurodegenerative diseases. What is not known is why protein degradation is impaired, allowing misfolded proteins to accumulate and become toxic in these diseases, or if the stimulation of the proteasome function could be a viable treatment. All of these diseases are characterized by their own unique protein deposits. However, the microtubule associated protein tau is unique in that it is ubiquitously implicated in most neurodegenerative diseases as the secondary protein involved in these protein deposits. The preliminary data that we have gathered led us to the central hypothesis that tau oligomers bind to the 20S proteasome, and inhibit protein degradation by stabilizing the closed gate conformation.
The first aim i n this proposal is to determine the molecular mechanism by which soluble tau oligomers impair the proteasome. This will allow us to identify and understand at a molecular level, a general mechanism of toxicity that could be common to many neurodegenerative diseases.
The second aim i n this proposal is to determine the feasibility of increasing proteasome activity to reduce toxicity due to the presence of specific oligomers in neuronal cell models. The proposal is expected to have an important and positive impact because it will allow us to identify and understand, at a molecular level, a general mechanism of toxicity in Alzheimer?s disease that could be common to many neurodegenerative diseases; and furthermore, it will assess the feasibility of reversing this toxicity to potentially treat neurodegenerative diseases.

Public Health Relevance

Approximately 5 million individuals across the United States suffer from Alzheimer?s disease, and the cost of care for this disease is estimated to be astronomical. Neurodegenerative diseases are characterized by the accumulation of misfolded proteins due to disruption of protein degradation systems, but what is not known, is the mechanism behind this disruption. The proposal is expected to have an important and positive impact because it will allow us to identify and understand, at a molecular level, a general mechanism of toxicity in Alzheimer?s disease that could be common to many neurodegenerative diseases; and furthermore, it will assess the feasibility of reversing this toxicity to potentially treat neurodegenerative diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
1F31AG058473-01
Application #
9469637
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Yang, Austin Jyan-Yu
Project Start
2017-12-01
Project End
2020-11-30
Budget Start
2017-12-01
Budget End
2018-11-30
Support Year
1
Fiscal Year
2017
Total Cost
Indirect Cost
Name
West Virginia University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
191510239
City
Morgantown
State
WV
Country
United States
Zip Code
26506