The central nervous system relies on a vast network of interconnected nerve cells to maintain physiological and behavioral homeostasis. Communication between the cells that comprise neuronal networks is mediated by the regulated secretion of chemical messengers. Through the work outlined in this proposal, we hope to better understand the molecular mechanisms which regulate the secretion of neurotransmitters and neuromodulators from nerve terminals. Our focus is on the proteins which comprise the critical organelle involved in synaptic transmission, the synaptic vesicle. We propose to further characterize molecules specifically localized to synaptic vesicles. Through an understanding of the interactions of these synaptic vesicle proteins with other components of the nerve terminal, we will gain insight into the functions of specific molecules. The availability of recombinant DNA clones encoding synaptic vesicle proteins makes it possible to introduce modified forms of the molecules into cells in culture and to study the resultant phenotypes. Understanding the mechanisms of synaptic transmission, as will be revealed by the experiments proposed here, is critical in defining the underlying defects that give rise to behavioral disorders. This research will aid in the prevention of psychiatric illness and the development of therapies for afflicted individuals.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37MH038710-14
Application #
2890315
Study Section
Special Emphasis Panel (NSS)
Program Officer
Asanuma, Chiiko
Project Start
1986-04-01
Project End
2002-04-30
Budget Start
1999-05-01
Budget End
2000-04-30
Support Year
14
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Stanford University
Department
Biophysics
Type
Schools of Medicine
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305