β-Arrestin: a Protein that Regulates β-adrenergic Receptor Function

Martin J. Lohse(Howard Hughes Medical Institute), Jeffrey Benovic(Howard Hughes Medical Institute), Juan Codina(Baylor College of Medicine), Marc G. Caron(Howard Hughes Medical Institute), Robert J. Lefkowitz(Howard Hughes Medical Institute)
Science
June 22, 1990
Cited by 1,210

Abstract

Homologous or agonist-specific desensitization of beta-adrenergic receptors is thought to be mediated by a specific kinase, the beta-adrenergic receptor kinase (beta ARK). However, recent data suggest that a cofactor is required for this kinase to inhibit receptor function. The complementary DNA for such a cofactor was cloned and found to encode a 418-amino acid protein homologous to the retinal protein arrestin. The protein, termed beta-arrestin, was expressed and partially purified. It inhibited the signaling function of beta ARK-phosphorylated beta-adrenergic receptors by more than 75 percent, but not that of rhodopsin. It is proposed that beta-arrestin in concert with beta ARK effects homologous desensitization of beta-adrenergic receptors.


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