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Isolation of plasma membranes from the bovine retinal pigment epithelium
Institution:1. Faculty of Bioscience Engineering, Department of Food Safety and Food Quality, Research Group Food Chemistry and Human Nutrition – nutriFOODchem (partner in Food2Know), Ghent University, Coupure Links 653, Ghent 9000, Belgium;2. Department of Food and Nutrition, Open University of Tanzania (OUT), P.O. Box 23409, Dar es Salaam, Tanzania;3. Nelson Mandela African Institute of Science and Technology, P.O. Box 447, Arusha, Tanzania;4. Tanzania Food and Drugs Authority, Directorate of Laboratory Services, Mabibo External, P. O. Box 77150, Dar es Salaam, Tanzania;5. Prince Leopold Institute of Tropical Medicine, Department of Public Health, Nutrition and Child Health Unit, Nationalestraat 155, Antwerp 2000, Belgium;1. Department of Biological and Environmental Sciences, Texas A&M University-Commerce, Commerce, TX 75429-3011, United States;2. Department of Drug Discovery and Development, Harrison School of Pharmacy, Auburn University, Auburn, AL 36849, United States
Abstract:Retinal pigment epithelium plasma membranes have been isolated by differential and density gradient centrifugation of glass-bead-bound, collagenase-treated cells. Electron microscopic evidence indicates that the glass-bead-bound cells were devoid of red blood cells, rod outer segments and other ocular cell contaminants. The plasma membranes were recovered in 4–6 μg/eye yields and purified 10-fold by 5′-nucleotidase and alkaline phosphodiesterase 1, and 6.5-fold by (Na+ + K+)-ATPase. Plasma membrane purity as measured by covalent labeling of the epithelial cell plasma membrane proteins with p-(diazonium) benzene32S]sulfonic acid was 8–19-fold. In purified plasma membranes contamination by mitochondria was undetectable and lysosomal contamination reduced 100-fold, while endoplasmic reticulum was 2-fold enriched. SDS-polyacrylamide gel electrophoresis of the plasma membrane proteins revealed 23–26 major bands by Coomassie blue staining and 12–16 major bands by radioactive labeling. The plasma membranes exhibited a 3-fold lower concentration of docosahexaenoic acid, a 3-fold higher cholesterol/phosphate ratio, and were 10-fold enriched in cholesterol per μg protein when compared to the whole cell fraction. Retinal epithelial plasma membranes contain an average of 1 mol cholesterol per mol of lipid phosphorus, a high palmitic acid concentration (39 mol%) and a low concentration of docosahexaenoic acid (2 mol%). The lipid profile of the retinal pigment epithelial plasma membranes indicates that they are typical of plasma membranes from many other cell types and that they appear to be less fluid than total rod outer segment membranes.
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