Stoichiometry of wheat germ agglutinin as a morphology controlling agent and as a morphology controlling agent and as a morphology protective agent for the human erythrocyte.
Open Access
- 1 June 1980
- journal article
- research article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 85 (3) , 534-548
- https://doi.org/10.1083/jcb.85.3.534
Abstract
The lectin wheat germ agglutinin (WGA) is an unusually effective agent in controlling the forward and reverse reactions of the reversible morphology conversion discocyte .dblarw. echinocyte for the human erythrocyte. Under conditions severe enough to drive the reactions to completion in either direction without the lectin, WGA is able to stabilize these morphologies and to fully prevent conversion of either morphology. The lectin can quantitatively block both reactions. The ability of WGA to carry out these functions has no obvious rate limitation. Its effectiveness depends mainly on its binding stoichiometry, particularly toward the transmembrane glycoprotein, glycophorin. The critical binding stoichiometries for the lectin and the echinocytic agent were determined in relation to the binding isotherms using 125I-labeled WGA and 35S-labeled dodecyl sulfate. Two apparent principal stoichiometries for WGA binding are important in its control of erythrocyte morphology. The 1st stoichiometry marks the threshold of obvious protection of the discocyte against strong echinocytic agents such as detergents and, likely, is simply a 1:1 stoichiometry of WGA: glycophorin, assuming currently recognized values of 3-5 .times. 105 copies of glycophorin/cell. The 2nd important stoichiometry, whereby the cell''s morphology is protected against extremely severe stress, involves binding of .apprx.4-5 WGA molecules/glycophorin. The controls that WGA exerts can be instantly abolished by added N-acetylglucosamine. N-acetylglucosamine ligands on the erythrocyte are of less importance than membrane neuraminic acid residues in enabling WGA to control the cell''s morphology, as is shown by comparing intact cells with completely desialated cells. WGA can be used to produce elliptocytes in vitro, but it does this at levels approaching monolayer coverage of the cell with WGA.This publication has 35 references indexed in Scilit:
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