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Molecular Pharmacology

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Research ArticleARTICLE

Influence of Agonist Efficacy and Receptor Phosphorylation on Antagonist Affinity Measurements: Differences between Second Messenger and Reporter Gene Responses

Jillian G. Baker, Ian P. Hall and Stephen J. Hill
Molecular Pharmacology September 2003, 64 (3) 679-688; DOI: https://doi.org/10.1124/mol.64.3.679
Jillian G. Baker
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Ian P. Hall
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Stephen J. Hill
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Abstract

The ability of an antagonist to bind to a receptor is an innate property of that ligand-receptor chemical interaction. Provided no change in the antagonist or receptor chemical nature occurs, this affinity should remain constant for a given antagonist-receptor interaction, regardless of the agonists used. This fundamental assumption underpins the classification of receptors. Here, measurements of β2-adrenoceptor-mediated cAMP accumulation and cAMP response-element (CRE)-mediated reporter-gene transcription revealed differences in antagonist affinity that depended upon agonist incubation time and the efficacy of the competing agonist. In cAMP accumulation studies (10-min agonist incubation), antagonist affinities were the same regardless of the agonist used. The CRE-reporter gene assay (5 h of incubation) antagonist affinities were 10-fold lower in the presence of isoprenaline and adrenaline than when salbutamol or terbutaline were present (e.g., log KD propranolol –8.65 ± 0.08, n = 22, and –9.68 ± 0.07, n = 17, for isoprenaline and salbutamol-induced responses, respectively). Isoprenaline and adrenaline were more efficacious in functional studies, and their ability to internalize GFP-tagged human β2-adrenoceptors. Longer-term cAMP studies also showed significant differences in KD values moving toward that seen with gene transcription. Agonist-dependent differences in antagonist affinity were reduced for reporter-gene responses when a phosphorylation-deficient mutant of the β2-adrenoceptor was used. This study suggests that high-efficacy agonists induce a chemical modification in β2-adrenoceptors (via phosphorylation) that reduces antagonist affinities. Because reporter-gene assays are used for high-throughput screening in drug discovery, less efficacious or partial agonists may be more reliable than highly efficacious agonists when reporter-gene techniques are used to estimate antagonist affinity.

  • Received February 10, 2003.
  • Accepted May 21, 2003.
  • The American Society for Pharmacology and Experimental Therapeutics
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Molecular Pharmacology: 64 (3)
Molecular Pharmacology
Vol. 64, Issue 3
1 Sep 2003
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Research ArticleARTICLE

Influence of Agonist Efficacy and Receptor Phosphorylation on Antagonist Affinity Measurements: Differences between Second Messenger and Reporter Gene Responses

Jillian G. Baker, Ian P. Hall and Stephen J. Hill
Molecular Pharmacology September 1, 2003, 64 (3) 679-688; DOI: https://doi.org/10.1124/mol.64.3.679

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Research ArticleARTICLE

Influence of Agonist Efficacy and Receptor Phosphorylation on Antagonist Affinity Measurements: Differences between Second Messenger and Reporter Gene Responses

Jillian G. Baker, Ian P. Hall and Stephen J. Hill
Molecular Pharmacology September 1, 2003, 64 (3) 679-688; DOI: https://doi.org/10.1124/mol.64.3.679
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