The binding of macromolecules (e.g. antibodies) and macromolecular assemblies (e.g. viruses) to cell surfaces is critical to a host of biologically and medically important processes. The current research proposal attempts to disclose the mechanistic details of such binding via the study of simple and controllable models involving the interaction of amphiphilic polymers with vesicular systems. The polymers are both negatively and positively charged, and they differ in their charge density and degree of polymerization. The vesicles with which they interact differ in curvature (small, large, and giant) and in their content of charged lipid. Association of the polymers with the vesicles will induce structural rearrangement, including lateral lipid segregation (""""""""domains""""""""), pore formation, and flip-flop all of which will be examined as a function of polymer and vesicle composition. Polymer-vesicle interaction has also been shown to affect transport of an antitumor drug, doxorubicin, an effect that will be further studied owing to its importance in the drug delivery arena. Finally, complexation of the polymers with DNA will be examined with respect to the association with, and transport through, the vesicular bilayers.

Agency
National Institute of Health (NIH)
Institute
Fogarty International Center (FIC)
Type
Small Research Grants (R03)
Project #
5R03TW005555-06
Application #
7169893
Study Section
International and Cooperative Projects 1 Study Section (ICP)
Program Officer
Katz, Flora N
Project Start
2001-05-15
Project End
2009-12-31
Budget Start
2007-01-01
Budget End
2009-12-31
Support Year
6
Fiscal Year
2007
Total Cost
$34,836
Indirect Cost
Name
Emory University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
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