ESR spin-label studies of lipid-protein interactions in membranes

• Published in: Biophysical journal Vol. 37; no. 1; pp. 265 - 274
• Main Authors: Marsh, D., Watts, A., Pates, R.D., Uhl, R., Knowles, P.F., Esmann, M.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 1982
• Subjects: Animals; Cattle; Chondrichthyes; Dimyristoylphosphatidylcholine; E.S.R; Electron Spin Resonance Spectroscopy; Electron Transport Complex IV - physiology; frogs; History of medicine; History, Medieval; In Vitro Techniques; Lipid Bilayers - physiology; lipids; Membrane Fluidity; Membranes - physiology; Models, Biological; Phosphatidylcholines; Photoreceptor Cells - physiology; proteins; Ranidae; rectal gland; Rod Cell Outer Segment - physiology; rod outer segment membranes; Salt Gland - enzymology; Sharks; Sodium-Potassium-Exchanging ATPase - physiology; Spin Labels; vesicles; Yeasts - enzymology
• ISSN: 0006-3495; 1542-0086
• DOI: 10.1016/S0006-3495(82)84675-4

Lipid spin labels have been used to study lipid-protein interactions in bovine and frog rod outer segment disc membranes, in (Na+, K+)-ATPase membranes from shark rectal gland, and in yeast cytochrome oxidase-dimyristoyl phosphatidylcholine complexes. These systems all display a two component ESR spectrum from 14-doxyl lipid spin-labels. One component corresponds to the normal fluid bilayer lipids. The second component has a greater degree of motional restriction and arises from lipids interacting with the protein. For the phosphatidylcholine spin label there are effectively 55 +/- 5 lipids/200,000-dalton cytochrome oxidase, 58 +/- 4 mol lipid/265,000 dalton (Na+, K+)-ATPase, and 24 +/- 3 and 22 +/- 2 mol lipid/37,000 dalton rhodopsin for the bovine and frog preparations, respectively. These values correlate roughly with the intramembrane protein perimeter and scale with the square root of the molecular weight of the protein. For cytochrome oxidase the motionally restricted component bears a fixed stoichiometry to the protein at high lipid:protein ratios, and is reduced at low lipid:protein ratios to an extent which can be quantitatively accounted for by random protein-protein contacts. Experiments with spin labels of different headgroups indicate a marked selectivity of cytochrome oxidase and the (Na+, K+)-ATPase for stearic acid and for cardiolipin, relative to phosphatidylcholine. The motionally restricted component from the cardiolipin spin label is 80% greater than from the phosphatidylcholine spin label for cytochrome oxidase (at lipid:protein = 90.1), and 160% greater for the (Na+, K+)-ATPase. The corresponding increases for the stearic acid label are 20% for cytochrome oxidase and 40% for (Na+, K+)-ATPase. The effective association constant for cardiolipin is approximately 4.5 times greater than for phosphatidylcholine, and that for stearic acid is 1.5 times greater, in both systems. Almost no specificity is found in the interaction of spin-labeled lipids (including cardiolipin) with rhodopsin in the rod outer segment disc membrane. The linewidths of the fluid spin-label component in bovine rod outer segment membranes are consistently higher than those in bilayers of the extracted membrane lipids and provide valuable information on the rate of exchange between the two lipid components, which is suggested to be in the range of 10(6)-10(7) s-1.