Recent advances in structure, binding sites with ligands and pharmacological function of β-adrenoceptors obtained by molecular biology and molecular modeling

被引:0
作者
Nagatomo, T
Koike, K
机构
[1] Niigata Coll Pharm, Dept Pharmacol, Niigata 9502018, Japan
[2] Toho Univ, Sch Pharmaceut Sci, Dept Chem Pharmacol, Chiba 2748510, Japan
关键词
beta-adrenoceptor; beta-blocker; binding site; interaction sites; molecular biology; molecular modeling; ligand-receptor interaction;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The structure, binding sites interacting with ligands and the physiological functions of G-protein coupled beta-adrenoceptors (beta-ARs) are being elucidated by molecular biology and molecular modeling studies. The definition given amino acid sequences of beta-ARs in molecular biology and the analysis of three-dimensional and functional binding sites interacting with ligands by molecular modeling may be important for identifying other functional beta-ARs in various tissues and discovering new drugs. Thus, this review focuses on the interaction sites for receptor-ligand and roles of functional beta-ARs as studied by molecular biology and molecular modeling.
引用
收藏
页码:2419 / 2426
页数:8
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