The overall goals of Dr. McIntosh's proposal are to determine the impact on important biological processes of short-and long-range interactions measured between lipid membranes. These interactions include entropic (steric) interactions due to membrane flexibility or motion of individual lipid molecules, and attractive and repulsive interactions caused by oriented dipoles in the membrane.
Specific aims i nclude determining: (1) the magnitude and origin of the adhesion energies of selected membrane glycolipids, including galactosyl- and glucosyl-ceramides, (2) the molecular organization and adhesive properties of the specialized ceramide-containing lipid lamellae that comprise the extracellular matrix of the skin stratum corneum, (3) the effects on both bilayer structure and interbilayer repulsive pressures of small peptides and lipophilic molecules that inhibit or promote cell fusion, (4) the influence of entropic pressures and dipolar electric fields on the binding of proteins to lipid membranes, and (5) the mechanism by which custom-designed polyphenolic molecules increase the adhesion between membranes. The research involves the combined use of x-ray and neutron diffraction/osmotic stress measurements of membrane structure and short-range interactions; resonance energy transfer and circular dichroism studies of peptide and protein binding; differential scanning calorimetry , dipole potential, microelectrophoresis, and micropipette analyses of bilayer thermal, electrostatic, and mechanical properties; and direct observations on in vivo extravasation of drug-containing liposomes. This fundamental basic research has several practical biomedical applications, including the development of intravenous and transdermal drug delivery systems and biocompatible coatings for medical implants.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM027278-19
Application #
6179422
Study Section
Physical Biochemistry Study Section (PB)
Program Officer
Lewis, Catherine D
Project Start
1980-07-01
Project End
2001-03-31
Budget Start
2000-04-01
Budget End
2001-03-31
Support Year
19
Fiscal Year
2000
Total Cost
$284,308
Indirect Cost
Name
Duke University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
McIntosh, Thomas J (2015) Stepping between membrane microdomains. Biophys J 108:783-784
Tong, Jihong; Canty, John T; Briggs, Margaret M et al. (2013) The water permeability of lens aquaporin-0 depends on its lipid bilayer environment. Exp Eye Res 113:32-40
Zhang, Xiao-Xiang; McIntosh, Thomas J; Grinstaff, Mark W (2012) Functional lipids and lipoplexes for improved gene delivery. Biochimie 94:42-58
Godeau, Guilhem; Navailles, Laurence; Nallet, Frédéric et al. (2012) From Brittle to Pliant Viscoelastic Materials with Solid State Linear Polyphosphonium - Carboxylate Assemblies. Macromolecules 45:2509-2513
Tong, Jihong; Briggs, Margaret M; McIntosh, Thomas J (2012) Water permeability of aquaporin-4 channel depends on bilayer composition, thickness, and elasticity. Biophys J 103:1899-908
LaManna, Caroline M; Lusic, Hrvoje; Camplo, Michel et al. (2012) Charge-reversal lipids, peptide-based lipids, and nucleoside-based lipids for gene delivery. Acc Chem Res 45:1026-38
Picazo-Juárez, Giovanni; Romero-Suárez, Silvina; Nieto-Posadas, Andrés et al. (2011) Identification of a binding motif in the S5 helix that confers cholesterol sensitivity to the TRPV1 ion channel. J Biol Chem 286:24966-76
Zhang, Xiao-Xiang; Prata, Carla A H; Berlin, Jason A et al. (2011) Synthesis, characterization, and in vitro transfection activity of charge-reversal amphiphiles for DNA delivery. Bioconjug Chem 22:690-9
Zhang, Xiao-Xiang; Prata, Carla A H; McIntosh, Thomas J et al. (2010) The effect of charge-reversal amphiphile spacer composition on DNA and siRNA delivery. Bioconjug Chem 21:988-93
Rosenbaum, Tamara; Simon, Sidney A; Islas, Leon D (2010) Ion channels in analgesia research. Methods Mol Biol 617:223-36

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