A method has been developed for the fractionation of human erythrocyte
membranes, using sodium deoxycholate, EDTA, differential ultracentrifugation, and
DEAE-cellulose column chromatography. Serologic studies demonstrate the presence of
ABO blood group antigens in a 50,000 g supernatant. This fraction is further purified
on DEAE-cellulose, and in type AB ghost preparations results in the separation of A
and B antigens. Phytohemagglutinin binding activity is also in the same supernatant and
after DEAE chromatography is located in the fraction that exhibited A activity. Rh and
MN activity is associated with a larger membrane fragment which is pelleted at 30,000 g.
The S, s, and I antigens are present in a soluble form, and remain in the supernatant following
centrifugation at 100,000 g.