A 43,000-dalton proteolytic fragment of the cytoplasmic domain of band 3 was purified, and monospecific antibodies against this fragment were prepared.1z61-Labeled 43,000-dalton fragment associated with pure ankyrin in solution, with a KO of 8 X lo"' M and with a stoichiometry of 0.85 mol of fragment/mol of ankyrin (with limiting concentrations of ankyrin).Anti-43,000dalton fragment IgG, which cross-reacted only with band 3, immunoprecipitated ankyrin, and band 4.2, as well as band 3 from detergent extracts of membranes, provided these were not denatured.1261-Labeled ankyrin associated selectively with the cytoplasmic surface of inside-out vesicles depleted of ankyrin as well as spectrin, actin, and bands 4.1,4.2,and 6.The binding of '2sI-labeled ankyrin was decreased over 90% by preincubating this protein above 54"C, or by preincubating the vesicles in 3 M guanidine.Scatchard plots of binding were biphasic, with high affinity (KO = 5 x M) and low affinity (KO = 1.4 X 10" M) components, and extrapolated to 65 to 75 p g of ankyrin/mg of ghost protein, or about 10' sites/erythrocyte.Selective proteolytic cleavage of vesicles and release of the cytoplasmic domain of band 3 abolished the high affinity binding of 12%labeled ankyrin, and decreased the number of low affinity sites by about 50%.Anti-43,OOO-dalton fragment IgG at 12 pg/ml inhibited over 90% of binding of low concentrations of '261-labeled ankyrin, and decreased binding by 60% at high concentrations of ankyri n.The 43,000-dalton fragment blocked binding of '2611-labeled ankyrin to vesicles by a competitive type of inhibition with a ki of 6.6 X 10" M.It is concluded that ankyrin and the cytoplasmic domain of band 3 associate directly without requirement for intermediary proteins, and that the cytoplasmic domain of band 3 participates, perhaps with other protein@), in attachment of ankyrin to the inner surface of the membrane.Human erythrocyte ankyrin (band 2.1') is a polypeptide of M, = 215,000 localized on the cytoplasmic surface of the membrane which has been identified as the high affinity membrane attachment site for spectrin (Bennett and Stenbuck, 1979a; Luna et al., 1979 Yu andGoodman, 1979).Association of spectrin with ankyrin has been demonstrated
No takes yet. Share an insight, caveat, or question.
Bennett et al. (1980) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: