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Biophysical Journal 52: 405-412 (1987)
© 1987 the Biophysical Society
Department of Medicine (Cardiology), Duke University Medical Center, Durham, North Carolina 27710.
ABSTRACT
Competitive ligand binding to periodically activated or accessible receptors is influenced by the interaction between ligand binding kinetics and the interval of time the binding site is accessible. This interaction produces a paradoxical reduction in bound receptors under certain conditions. A mathematical description of multi-ligand binding to a single binding site is presented for both the continuously and transiently accessible cases. The theoretical results predict paradoxical "agonism" and are consistent with the results of studies of lidocaine and bupivacaine binding to cardiac sodium channels.
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