This research seeks to exploit a new technique to study the biophysics and biochemistry of """"""""cell-cell recognition,"""""""" especially involving cellular components of the immune system. The new technique, dubbed the evanescent wave, supported lipid monolayer (EWSM) technique, replaces one cell of a cell-cell pair by a lipid monolayer a solid support such as a microscope slide. When specific molecules that link a cell to the monolayer are fluorescent, then the linker molecules that are within about 700/Angstroms of the monolayer membrane are stimulated to emit when a laser beam undergoes total external reflection in the microscope slide. Using this technique, information on the motion and distribution of molecules involved in specific cell-membrane, monolayer membrane binding and triggering can be observed with a fluorescence microscope, for molecules such as lipid haptens, antibodies, viral proteins, and histocompatibility antigens. The unique information obtainable indicates that the EWSM technique can be used to guide biochemical experiments such as the identification and isolation of cell membrane receptors, especially the elusive T-cell receptor. In such experiments, selected cross-linking agents are included in the lipid monolayer so as to bond only to those cell plasma membrane components that bind specifically to the monolayer.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI013587-12
Application #
3125500
Study Section
Biophysics and Biophysical Chemistry B Study Section (BBCB)
Project Start
1976-05-01
Project End
1989-04-30
Budget Start
1987-05-01
Budget End
1988-04-30
Support Year
12
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Stanford University
Department
Type
Schools of Arts and Sciences
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
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Hall, Frances C; Visconti, Kevin C; Ahmad, Regina-Celeste et al. (2003) Cytokines elicited by T cell epitopes from a synovial autoantigen: altered peptide ligands can reduce interferon-gamma and interleukin-10 production. Arthritis Rheum 48:2375-85
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McConnell, Harden M; Radhakrishnan, Arun (2003) Condensed complexes of cholesterol and phospholipids. Biochim Biophys Acta 1610:159-73
Hall, Frances C; Rabinowitz, Joshua D; Busch, Robert et al. (2002) Relationship between kinetic stability and immunogenicity of HLA-DR4/peptide complexes. Eur J Immunol 32:662-70
Belmares, Michael P; Busch, Robert; Wucherpfennig, Kai W et al. (2002) Structural factors contributing to DM susceptibility of MHC class II/peptide complexes. J Immunol 169:5109-17
Vrljic, Marija; Nishimura, Stefanie Y; Brasselet, Sophie et al. (2002) Translational diffusion of individual class II MHC membrane proteins in cells. Biophys J 83:2681-92
Radhakrishnan, Arun; McConnell, Harden M (2002) Critical points in charged membranes containing cholesterol. Proc Natl Acad Sci U S A 99:13391-6
Anderson, Thomas G; McConnell, Harden M (2002) A thermodynamic model for extended complexes of cholesterol and phospholipid. Biophys J 83:2039-52

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