Shared determinants of receptor binding for subtype selective, and dual endothelin-angiotensin antagonists on the AT1 angiotensin II receptor

被引:16
作者
Dascal, D
Nirula, V
Lawus, K
Yoo, SE
Walsh, TF
Sandberg, K
机构
[1] Georgetown Univ, Med Ctr, Dept Med, Washington, DC 20007 USA
[2] Korea Res Inst Chem Technol, Taejon 305343, South Korea
[3] Merck Res Labs, Dept Med Chem, Rahway, NJ 07065 USA
关键词
angiotensin; endothelin; AT(1) receptor; non-peptide; biphenylimidazole; dual receptor antagonist;
D O I
10.1016/S0014-5793(98)00040-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Site-directed interspecies amino acid exchange mas used to compare the binding determinants of a novel dual endothelial-angiotensin receptor Ligand, L-746,072, with type-1 angiotensin receptor (AT(1)) selective antagonists on AT receptors expressed in COS cells, These studies suggest that residues on AT receptors which are non-conserved between amphibian and mammalian species play a greater role in subtype selective ligand recognition than for dual receptor ligands, These data also support the hypothesis that a common non-peptide binding site exists within transmembrane domains on peptidergic receptors. (C) 1998 Federation of European Biochemical Societies.
引用
收藏
页码:15 / 18
页数:4
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