Interactions between conserved residues in transmembrane helices 2 and 7 during angiotensin AT1 receptor activation

Gregory V. Nikiforovich, Meng Zhang, Qing Yang, Gowraganahalli Jagadeesh, Hao Chia Chen, László Hunyady, Garland R. Marshall, Kevin J. Catt

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Abstract

Site-directed mutagenesis studies and independent molecular modeling studies were combined to investigate the network of inter-residue interactions within the transmembrane region of the angiotensin AT1a receptor. Site-directed mutagenesis was focused on residues Tyr292, Asn294, Asn295, and Asn298 in transmembrane helix 7, and the conserved Asp74 in helix 2 and other polar residues. Functional interactions between pairs of residues were evaluated by determining the effects of single and double-reciprocal mutations on agonist-induced AT1a receptor activation. Replacement of Tyr292 by aspartate in helix 7 abolished radioligand binding to both Y292D and D74Y/Y292D mutant receptors. Reciprocal mutations of Asp74/Asn294, Ser115/Asn294, Ser252/Asn294, and Asn298/Sen115 caused additive impairment of function, suggesting that these pairs of residues make independent contributions to AT1a receptor activation. In contrast, mutations of the Asp74/Tyr298 pair revealed that the D74N/N298D reciprocal mutation substantially increased the impaired inositol phosphate responses of the D74N and N298D receptors. Extensive molecular modeling yielded 3D models of the TM region of the AT 1 receptor and the mutants as well as of their complexes with angiotensin II, which were used to rationalize the possible reasons of impairing of function of some mutants. These data indicate that Asp74 and Asn298 are not optimally positioned for direct strong interaction in the resting conformation of the AT1a receptor. Balance of interactions between residues in helix 2 (as D74) and helix 7 (as N294, N295 and N298) in the AT1 receptors, however, has a crucial role both in determining their functional activity and levels of their expression.

Original languageEnglish
Pages (from-to)239-249
Number of pages11
JournalChemical Biology and Drug Design
Volume68
Issue number5
DOIs
Publication statusPublished - Nov 1 2006

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Keywords

  • Angiotensin receptor type 1
  • G protein-coupled receptors
  • Molecular modeling
  • Site- directed mutagenesis

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Medicine
  • Pharmacology
  • Drug Discovery
  • Organic Chemistry

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