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J. Biol. Chem., Vol. 263, Issue 35, 18776-18784, 12, 1988
WL Roberts, S Santikarn, VN Reinhold and TL Rosenberry
The glycoinositol phospholipid membrane anchor of human erythrocyte
acetylcholinesterase (EC 3.1.1.7) is composed of a glycan linked through a
glucosamine residue to an inositol phospholipid that is resistant to the
action of phosphatidylinositol-specific phospholipase C. Deamination
cleavage of the glucosamine with nitrous acid released the inositol
phospholipid which was purified by high performance liquid chromatography.
Analysis by fast atom bombardment mass spectrometry with negative ion
monitoring and by the complementary technique of collision-induced
dissociation revealed molecular and daughter ions that indicated a
plasmanylinositol with a palmitoyl group on an inositol hydroxyl. The
intact membrane anchor was released from reductively methylated human
erythrocyte acetylcholinesterase by proteolysis with papain or Pronase,
deacylated by base hydrolysis, and purified by high performance liquid
chromatography. Positive and negative ion fast atom bombardment mass
spectrometry of the major products isolated by high performance liquid
chromatography indicated the following structure for the complete
glycoinositol phospholipid anchor. (formula; see text) Methylation of free
amino groups by reduction with deuterium instead of hydrogen permitted
determination of the number of free amino groups in individual fragment
ions as further confirmation of structural assignments. The structure of
the glycan portion of the human erythrocyte acetylcholinesterase membrane
anchor appears to be similar to that described for Trypanosome brucei
variant surface glycoprotein MITat 1.4 (variant 117) (Ferguson, M.A.J.,
Homans, S.W., Dwek, R.A., and Rademacher, T.W. (1988) Science 239, 753-759)
except for the absence of a galactose antenna and the presence of a
phosphorylethanolamine on the hexose adjacent to glucosamine.
Structural characterization of the glycoinositol phospholipid membrane anchor of human erythrocyte acetylcholinesterase by fast atom bombardment mass spectrometry
Department of Pharmacology, School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106.
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