Awardee OrganizationUNIVERSITY OF CALIF-LAWRENC BERKELEY LAB
Description
Abstract Text
DESCRIPTION (provided by applicant): Cells interact with each other and their
environment through myriad membrane associated receptors and signaling
molecules. In addition to individual receptor-ligand binding, spatial
rearrangement of receptors into complex patterns (synapses) is rapidly emerging
as a broadly significant aspect of cell recognition. Two prominent examples,
which will be the foci of this investigation, are the T-cell and NK-cell
immunological synapses. The PI's are mounting a quantitative investigation of
the physical characteristics and principles governing the reorganization events
that lead to synapse formation. They have developed a theoretical model, which
compares well with experimental observations, and suggests that the essential
features of immunological synapse formation are the result of spontaneous
self-organization processes. Here, they propose to test and develop this
hypothesis. A three-pronged investigative platform, that combines sophisticated
theoretical calculations and computer simulations with novel membrane
experiments in reconstituted lipid membranes and living cells, has been
formulated to meet the specific aims. In aim 1, they develop sophisticated
theoretical and computational tools, and use these methods and experiments to
understand the differential morphology of T cell and NK cell synapses. In aim
2, they perform a stability analysis of their model and this, in conjunction
with experiments, will allow them to study how key cell surface parameters
regulate synapse formation. In aim 3, they determine the effects of regulatory
factors within the cell on synapse formation. In aim 4, will use a genetic
algorithm to explore other synaptic patterns and will perform experiments to
determine if such patterns can be observed based on the current vocabulary of
known molecular interactions and cell types, or based on synthetic
interactions. These studies will provide a deep and quantitative understanding
of synaptic pattern formation in the immune system and may lead to novel
biomimetic and therapeutic approaches.
No Sub Projects information available for 5R01GM064900-02
Publications
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Patents
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Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
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Clinical Studies
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History
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