Synaptic activity depends on constant cycles of protein complex formation and dissociation, from the SNARE complexes that induce synaptic vesicle fusion to the clathrin:clathrin and clathrin:adaptor interactions required for endocytic retrieval of SV proteins. Regulating the assembly and disassembly of these complexes is the job of molecular chaperones, particularly the Hsp70s and their co-chaperone regulators. Chaperone dysfunction results in aggregation of the highly interactive proteins that form these complexes, and leads to neuronal dysfunction and neurodegeneration, induced either by aggregation-driven depletion of essential proteins or the toxic effects of the aggregates themselves. An understanding of chaperone mechanisms is therefore essential to understanding basic synaptic mechanisms and to understanding and treating neurodegenerative disease. Chaperones also have multiple functions in all cell types, and this adds to the significance of elucidating their mechanisms. Over the previous project period our focus on the roles and mechanisms of molecular chaperones in synaptic function has increased. We now propose to pursue the following broad themes: (1) Characterization of the structures, mechanisms, and regulation of two chaperones--Hsp110 and Hip--that have been relatively understudied, but that are highly abundant in brain and that have demonstrated roles in neuronal function or neurodegenerative disease. (2) Elucidation of the role of chaperone:chaperone associations in chaperone function and inhibition of neurodegenerative disease. This work is expected to advance our fundamental understanding of the mechanisms that underlie synaptic transmission, and as such will be a critical part of our efforts to fight neurological disorders.

Public Health Relevance

This work is focused on understanding the roles and mechanisms of molecular chaperones in synaptic function. Chaperones are involved in synaptic transmission, the process used by neurons to communicate with each other. A common feature of many neurological disorders is aberrant synaptic transmission, so this work will be important for understanding and developing therapeutic strategies that will enable clinical intervention. Moreover, the chaperone proteins that we will study are also involved in many diseases that are a consequence of the accumulation of damaged, aggregated proteins (Alzheimer's, ALS, Parkinson's, Huntington's, and others), so this work will also be relevant to the fight against neurodegenerative disorders.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
High Priority, Short Term Project Award (R56)
Project #
2R56NS029051-25
Application #
8739988
Study Section
Special Emphasis Panel (ZRG1-MDCN-G (02))
Program Officer
Talley, Edmund M
Project Start
1987-04-01
Project End
2014-08-31
Budget Start
2013-09-28
Budget End
2014-08-31
Support Year
25
Fiscal Year
2013
Total Cost
$373,750
Indirect Cost
$123,750
Name
University of Texas Health Science Center San Antonio
Department
Biochemistry
Type
Schools of Medicine
DUNS #
800772162
City
San Antonio
State
TX
Country
United States
Zip Code
78229
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