This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator.Among the proteins that are interacting candidates of the Urokinase Plasminogen Activator Receptor (uPAR), vitronectin (Vn) is thought to specifically dictate the uPAR monomer-dimer exchange and dynamics at the cell membrane. When cells expressing uPAR are seeded on Vn coated plates, dimers of uPAR should form and be recruited for cell adhesion. Alternatively, coating of Fn, which does not bind uPAR, should not induce the dimerization of the receptor at the adhesion sites of the cell.Dimers will be detected using the new phasor-FLIM analysis of TCSPC decays of uPAR-GFP co-transfected with uPAR-mRFP1 in HEK293 cells

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR003155-23
Application #
7724035
Study Section
Special Emphasis Panel (ZRG1-BCMB-E (41))
Project Start
2008-08-01
Project End
2009-07-31
Budget Start
2008-08-01
Budget End
2009-07-31
Support Year
23
Fiscal Year
2008
Total Cost
$74,514
Indirect Cost
Name
University of California Irvine
Department
Biomedical Engineering
Type
Schools of Engineering
DUNS #
046705849
City
Irvine
State
CA
Country
United States
Zip Code
92697
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