This proposal is aimed at understanding fundamental aspects of membrane fusion in neurons. Membrane fusion is mediated by SNARE proteins (v-SNAREs on the vesicle membrane, t-SNAREs on the target membrane) and is tightly controlled by regulatory factors. We have largely focused on the Ca2+triggered exocytosis of synaptic vesicles, which is controlled by the Ca2+binding protein synaptotagmin (syt) 1. Syt I operates through direct physical interactions with t-SNAREs and membranes. This proposal continues our studies of syt I but also extends our work to address the functions of the other fifteen isoforms of this protein.
Aim 1 a employs a defined reconstituted system to test the hypothesis that the syt gene family has diverged in ways that help confer specificity to intracellular membrane fusion reactions. We hypothesize that specificity is achieved, in part, through selective pairing between different isoforms of syt and t-SNAREs in various sub-cellular compartments. We will determine the syt-SNARE pairing-code and compare this with the distribution of these proteins in neurons.
In Aim 1 b we continue to pursue our goal of reconstituting rapid membrane fusion that recapitulates the rapid kinetics of synaptic vesicle exocytosis in neurons. This is a key step toward defining the precise molecular mechanism that underlies exocytosis.
In Aim 2 we will bridge the gap between the minimal fusion assay used in Aim 1 and studies of synaptic transmission (e.g.
Aim 3 below), by analyzing directly the fusion activity of synaptic vesicles isolated from knock-out/knock-in mice. This approach compliments electrophysiological analysis because it reports the intrinsic fusion properties of vesicles lacking specific proteins. These experiments will also make it possible to address the function of synaptic vesicle proteins that we have been unable to reconstitute in an active form in Aim 1.
In Aim 3, we will test the hypothesis that different isoforms of syt have diverged to impart synapses with distinct kinetic components of release. We predict that syt isoforms with fast kinetics mediate synchronous transmission, while syt isoforms with slower kinetics mediate asynchronous transmission. These studies will provide new insights into information flow in neuronal circuits. Together, the experiments proposed here will provide critical information regarding our understanding of membrane fusion at synapses. This will aid efforts to alter communication between neurons in disease states where synaptic transmission is impaired.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH061876-09
Application #
8085793
Study Section
Synapses, Cytoskeleton and Trafficking Study Section (SYN)
Program Officer
Asanuma, Chiiko
Project Start
2002-03-01
Project End
2013-04-14
Budget Start
2011-07-01
Budget End
2013-04-14
Support Year
9
Fiscal Year
2011
Total Cost
$287,158
Indirect Cost
Name
University of Wisconsin Madison
Department
Physiology
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Bao, Huan; Das, Debasis; Courtney, Nicholas A et al. (2018) Dynamics and number of trans-SNARE complexes determine nascent fusion pore properties. Nature 554:260-263
Chapman, Edwin R (2018) A Ca2+ Sensor for Exocytosis. Trends Neurosci 41:327-330
Xue, Renhao; Ruhl, David A; Briguglio, Joseph S et al. (2018) Doc2-mediated superpriming supports synaptic augmentation. Proc Natl Acad Sci U S A 115:E5605-E5613
Courtney, Nicholas A; Briguglio, Joseph S; Bradberry, Mazdak M et al. (2018) Excitatory and Inhibitory Neurons Utilize Different Ca2+ Sensors and Sources to Regulate Spontaneous Release. Neuron 98:977-991.e5
Bendahmane, Mounir; Bohannon, Kevin P; Bradberry, Mazdak M et al. (2018) The synaptotagmin C2B domain calcium-binding loops modulate the rate of fusion pore expansion. Mol Biol Cell :
Rao, Tejeshwar C; Santana Rodriguez, Zuleirys; Bradberry, Mazdak M et al. (2017) Synaptotagmin isoforms confer distinct activation kinetics and dynamics to chromaffin cell granules. J Gen Physiol 149:763-780
Zurawski, Zack; Page, Brian; Chicka, Michael C et al. (2017) G?? directly modulates vesicle fusion by competing with synaptotagmin for binding to neuronal SNARE proteins embedded in membranes. J Biol Chem 292:12165-12177
Ugur, Berrak; Bao, Huan; Stawarski, Michal et al. (2017) The Krebs Cycle Enzyme Isocitrate Dehydrogenase 3A Couples Mitochondrial Metabolism to Synaptic Transmission. Cell Rep 21:3794-3806
Hanna 4th, Michael G; Mela, Ioanna; Wang, Lei et al. (2016) Sar1 GTPase Activity Is Regulated by Membrane Curvature. J Biol Chem 291:1014-27
McVicker, Derrick P; Awe, Adam M; Richters, Karl E et al. (2016) Transport of a kinesin-cargo pair along microtubules into dendritic spines undergoing synaptic plasticity. Nat Commun 7:12741

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