RRC ID 6551
著者 Hossain M, Ahmed M, Bhuiyan MA, Ishiguro M, Nakamura T, Ozaki M, Nagatomo T.
タイトル Mutation of important amino acid residue of Asp104Lys in human beta(1)-adrenergic receptor triggers functional and constitutive inactivation.
ジャーナル Biol Pharm Bull
Abstract Based on our previous molecular modeling and radioligand binding study, we have demonstrated that aspartic acid of 104 in transmembrane helix (TMH) II of beta(1)-adrenergic receptor (beta(1)-AR) is important for functional characteristics of these receptors. We have also showed that mutation of negatively charged aspartic acid to neutral charged alanine exhibited constitutive activity of beta(1)-AR. However, the mutation of negatively charged aspartic acid to positively charged lysine is still remained to be examined, which is very important to know for fully understanding the characteristics of beta(1)-AR. At the present study, we mutated aspartic acid to lysine (Asp104Lys) residue in human beta(1)-AR. This resultant mutant (Asp104Lys) markedly reduced the binding affinity of isoproterenol and (-)-epinephrine. On the other hand, antagonist binding with this mutant was similar to the wild type receptor. Isoproterenol at its saturation concentrations produced lower amount of intracellular cyclic adenosine-3',5' cyclic monophosphate (cAMP) in HEK-293 cells expressing Asp104Lys mutant receptor as compared to cells expressing wild type receptor. Moreover, cAMP accumulation of Asp104Lys mutant was unchanged in the presence or absence of isoproterenol. Therefore, it has been demonstrated that Asp104Lys mutation in the human beta(1)-AR differentially affects the binding of antagonist and exhibits a functional uncoupling of G-protein-coupled receptors. Thus, we may suggest that mutation of negatively charged aspartic acid to positively charged lysine as well as neutral charged alanine may help to understand the mechanism of the activation or inactivation of beta(1)-AR by its conformational changes and this finding would be helpful for clarifying the functional responses mediated by beta(1)-AR.
巻・号 31(8)
ページ 1517-22
公開日 2008-8-1
DOI 10.1248/bpb.31.1517
PII JST.JSTAGE/bpb/31.1517
PMID 18670082
MeSH Adrenergic beta-Agonists / metabolism Adrenergic beta-Agonists / pharmacology Adrenergic beta-Antagonists / metabolism Adrenergic beta-Antagonists / pharmacology Amino Acid Substitution Binding, Competitive / drug effects Blotting, Western Cyclic AMP / metabolism DNA, Complementary / biosynthesis DNA, Complementary / genetics Humans Isoproterenol / pharmacology Mutagenesis, Site-Directed Mutation / physiology Radioligand Assay Receptors, Adrenergic, beta-1 / drug effects* Receptors, Adrenergic, beta-1 / genetics* Receptors, Adrenergic, beta-1 / metabolism Receptors, G-Protein-Coupled / physiology Transfection
IF 1.863
引用数 4
WOS 分野 PHARMACOLOGY & PHARMACY
リソース情報
ヒト・動物細胞