An Unusual Mechanism for Ligand Antagonism

Author:

Torigoe Chikako1,Inman John K.1,Metzger Henry1

Affiliation:

1. C. Torigoe and H. Metzger, Arthritis and Rheumatism Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892–1820, USA. J. K. Inman, Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892–1820, USA.

Abstract

The ratio of late to early events stimulated by the mast cell receptor for immunoglobulin E (IgE) correlated with the affinity of a ligand for the receptor-bound IgE. Because excess receptors clustered by a weakly binding ligand could hoard a critical initiating kinase, they prevented the outnumbered clusters engendered by the high-affinity ligands from launching the more complete cascade. A similar mechanism could explain the antagonistic action of some peptides on the activation of T cells.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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