The general objective of our proposed research is to characterize and compare dissipative processes that occur in the plane of composite membranes of human red cells and lamellar lipid systems. Transport phenomena in the plane of the membrane are limited by these dissipative processes, represented by coefficients of surface viscosity and surface diffusivity. With complex membrane materials such as the red cell membrane, dissipation rates are specific to the regime of material behavior being investigated, i.e., solid, semi-solid and liquid (plastic). The behavior of the material is characterized by viscoelastic recovery, """"""""creep"""""""" and relaxation, and viscoplastic flow experiments. Dissipative behavior in these general material regimes will be studied as a function of temperature, and duration and magnitude of applied membrane forces. The transition from solid to liquid-like behavior in complex membranes is especially significant and represents permanent structural alteration or rearrangement which depends on molecular relaxation processes in the composite membrane. Simple membranes such as lamellar lipid systems (above the phase transition for ordered acyl chains) behave only as surface liquids. The state of the lipid membrane is altered by changes in temperature and surface density (produced by changes in membrane tension). Dissipation in lipid bilayers will be studied by measuring the changes in surface (lateral) diffusivity of specific membrane marker particles. Membranes forces and deformations will be produced using micromanipulation methods on human red cells and large lipid vesicles. The time dependent state of red cell membrane deformation and the fluorescence recovery of bleached fluorophores in lipid membranes will be used to determine the coefficients of surface viscosity and surface diffusivity, respectively.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL023728-06
Application #
3337401
Study Section
Surgery and Bioengineering Study Section (SB)
Project Start
1979-04-01
Project End
1985-11-30
Budget Start
1984-12-01
Budget End
1985-11-30
Support Year
6
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Duke University
Department
Type
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
Hochmuth, Robert M; Marcus, Warren D (2002) Membrane tethers formed from blood cells with available area and determination of their adhesion energy. Biophys J 82:2964-9
Marcus, Warren D; Hochmuth, Robert M (2002) Experimental studies of membrane tethers formed from human neutrophils. Ann Biomed Eng 30:1273-80
Levin, J D; Ting-Beall, H P; Hochmuth, R M (2001) Correlating the kinetics of cytokine-induced E-selectin adhesion and expression on endothelial cells. Biophys J 80:656-67
Hochmuth, R M (2000) Micropipette aspiration of living cells. J Biomech 33:15-22
Dai, J; Ting-Beall, H P; Hochmuth, R M et al. (1999) Myosin I contributes to the generation of resting cortical tension. Biophys J 77:1168-76
Shao, J Y; Hochmuth, R M (1999) Mechanical anchoring strength of L-selectin, beta2 integrins, and CD45 to neutrophil cytoskeleton and membrane. Biophys J 77:587-96
Gerald, N; Dai, J; Ting-Beall, H P et al. (1998) A role for Dictyostelium racE in cortical tension and cleavage furrow progression. J Cell Biol 141:483-92
Shao, J Y; Ting-Beall, H P; Hochmuth, R M (1998) Static and dynamic lengths of neutrophil microvilli. Proc Natl Acad Sci U S A 95:6797-802
Shao, J Y; Hochmuth, R M (1997) The resistance to flow of individual human neutrophils in glass capillary tubes with diameters between 4.65 and 7.75 microns. Microcirculation 4:61-74
Shao, J Y; Hochmuth, R M (1996) Micropipette suction for measuring piconewton forces of adhesion and tether formation from neutrophil membranes. Biophys J 71:2892-901

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