? We propose experiments that have significance at two levels. First we will continue to develop and prove the effectiveness of our recently developed, transgenically encoded technique for protein photoinactivation in vivo. If we continue to be successful in this arena, it will substantiate this technique and encourage the use of this approach in other transgenic systems. This technique has the potential to be broadly applicable to diverse areas of basic research in cell biology, neuroscience, cancer and stem cell biology. Second, we propose to use our technique of protein photoinactivation to further dissect the molecular mechanisms that control synaptic vesicle endocytosis in vivo. Synaptic vesicle endocytosis is essential for the maintenance of appropriate neural function in the nervous system. It has been hypothesized that rapid, clathrin-independent endocytosis occurs at the neuronal synapse and that this form of endocytosis is necessary to maintain a releasable pool of synaptic vesicles. However, because clathrin mutations are early embryonic lethal it has not been possib]e to eliminate clathrin assembly at a mature neuronal synapse and directly test whether clathrin-independent endocytosis exists. Dominant interfering approaches have been attempted but in no case has it been possible to eliminate clathrin function at a mature synapse. We propose to photoinactivate clathrin heavy chain (Chc) and block clathrin assembly over a timecourse of seconds to minutes. If we observe clathrin-independent endocytosis following photoinactivation we will then be able to study this form of synaptic vesicle endocytosis in isolation, and we will do so in vivo. Regardless of the experimental outcome, we will also be able to use our new tools to pursue a new generation of experiments examining the molecular mechanisms of clathrin-dependent endocytosis in vivo. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21MH072698-01
Application #
6848910
Study Section
Synapses, Cytoskeleton and Trafficking Study Section (SYN)
Program Officer
Asanuma, Chiiko
Project Start
2004-09-30
Project End
2006-08-31
Budget Start
2004-09-30
Budget End
2005-08-31
Support Year
1
Fiscal Year
2004
Total Cost
$189,652
Indirect Cost
Name
University of California San Francisco
Department
Biochemistry
Type
Schools of Medicine
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Heerssen, Heather; Fetter, Richard D; Davis, Graeme W (2008) Clathrin dependence of synaptic-vesicle formation at the Drosophila neuromuscular junction. Curr Biol 18:401-9
Thompson, Scott M; Kao, Joseph P Y; Kramer, Richard H et al. (2005) Flashy science: controlling neural function with light. J Neurosci 25:10358-65