? The goal of this project is to design, synthesize, and test the requirements for a multivalent ligand to bind simultaneously to erythrocytes and blood borne pathogens and clear the latter from circulation by directing them to the liver. The ligand will be comprised of a ring opening metathesis polymerization (ROMP)-derived block copolymer functionalized with antibody fragments (Fab'). Half of the polymer will contain Fab' targeted against complement receptor type 1 (CR1) receptors on the surface of erythrocytes, while the other half will be functionalized with Fab' against Staphylococcus aureus. This project is based on the knowledge that randomly cross-linked antibody complexes specific for both CR1 and surface antigens on other cells are able to aggregate the two cell types and deliver the nonerythrocyte to be destroyed in the liver. The multivalent ligand proposed offers significant improvement over previous attempts towards similar goals through the use of structural homogeneity. If successful, the result of this project will be a powerful method for the rapid and general removal of pathogens from circulation. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32AI060305-01
Application #
6793362
Study Section
Special Emphasis Panel (ZRG1-F04 (20))
Program Officer
Peters, Kent
Project Start
2004-04-01
Project End
2007-03-31
Budget Start
2004-04-01
Budget End
2005-03-31
Support Year
1
Fiscal Year
2004
Total Cost
$41,068
Indirect Cost
Name
University of Wisconsin Madison
Department
Biochemistry
Type
Schools of Earth Sciences/Natur
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715