Abstract

In erythrocytes treated with 2,4,6-trinitrobenzenesulfonate (a non-penetrating probe) for 24 hours, a maximum of 33% of the phosphatidylethanolamine and none of the phosphatidylserine reacts with this reagent. In erythrocyte ghosts, however, 95% of the phosphatidylethanolamine and over 50% of the phosphatidylserine reacts in 90 minutes under the same conditions. When extracted erythrocyte lipids are treated with 2,4,6-trinitrobenzenesulfonate in either a chloroform-methanolbicarbonate or a sonicated aqueous bicarbonate system, both phosphatidylethanolamine and phosphatidylserine react essentially to completion within minutes. We interpret these results to indicate the localization of nearly all of the phosphatidylserine on the interior surface of the membrane thus demonstrating an asymmetric distribution of phospholipids in the erythrocyte membrane.

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