Interaction of Digitonin and Its Analogs with Membrane Cholesterol1

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Abstract
The interaction of digitonin with membrane cholesterol was studied by using variousdigitonin analogs, and radioactive desglucodigitonin. The following results were obtained concerning the effect of digitonin on erythrocytes, granulocytes and liposomes. 1. Digitonin and its analogs showed activity to induce hemolysis, granulocyteactivation and liposomal membrane damage. The activity was affected by changeof the carbohydrate residue of the molecule; the order of hemolytic activity was digitonin ⋛ desglucodigitonin ≫ glucosyl-galactosyl-digitogenin > galactosyl-digito-genin, digitogenin. The relative activities of these compounds to induce granulocyteactivation and liposomal membrane damage were similar to those observed in thehemolysis. 2. [3H]Desglucodigitonin could bind to cholesterol in liposomes. The binding was stoichiometric and the ratio of desglucodigitonin bound to liposomes/cholesterol in liposomes was close to 1, irrespective of the cholesterol content in liposome. Damage to liposomes was, however, induced by desglucodigitonin only when they contained more than 0.2 molar ratio of cholesterol to phospholipid. 3. Addition of digitonin as well as desglucodigitonin to preformed liposomes deprived of cholesterol affected the anisotropic molecular motion of spin-labeled phosphatidylcholine incorporated into the liposomes, suggesting that the molecules could be inserted into the lipid bilayer free of cholesterol. Molecules of desglucodigitonin in the lipid phase may, however, be equilibrated with those in the aqueous phase, unless they form a complex with cholesterol, since no appreciable amount of PH]desglucodigitonin could be detected in the liposome fraction after separation by column chromatography. 4. Digitonin decreased the order parameter of spin-labeled phosphatidylcholine when liposomes contained equimolar cholesterol. This finding, together with the restoration of the phase transition of phosphatidylcholine by digitonin, suggests that digitonin may form a complex with cholesterol, producing cholesterol-free domains on the membranes.