Abstract

Several proteins including bovine erythrocyte acetylcholinesterase are anchored in the membrane through glycoinositol phospholipids containing an alkyl linkage at the sn -1 position of the glycerol. However, the existence of 1-alkyl-2-acyl- sn -glycero-3-phosphoinositol (alkylacyl-GPI) in biological systems has not been demonstrated. In this study, we identified the presence of alkylacyl-GPI in bovine erythrocytes by the following criteria: (1) TLC-R f value, (2) radyllyso-GPI was produced after phospholipase A 2 treatment of the diradyl-GPI, and (3) benzoate derivatives of alkylacylglycerols produced by phospholipase C hydrolysis of diradyl-GPI had the same retention time as that of authentic alkylacylglycerobenzoates on normal-phase HPLC. Diradyl-GPI consisted of 5–10% alkylacyl-GPI. Reverse-phase HPLC analysis of alkylacylglycerobenzoates derived from bovine erythrocyte alkylacyl-GPI showed a multiplicity of species with 18:0–20:4 (11.7%), 16:0–18:1 + 18:0–18:2 (34.9%), and 18:0–18:1 (19.4%) being the major components. Composition of alkyl chains of alkylacyl-GPI from bovine erythrocytes was similar to the reported value for alkylacylglycerols isolated from the glycoinositol phospholipid anchor of bovine erythrocyte acetylcholinesterase. Based on these results, we suggest that alkylacyl-GPI serves as a precursor for the glycoinositol phospholipid of the anchored proteins.

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