Cotecchia S, Rossier O, Fanelli F, Leonardi A, De Benedetti P G
Institut de Pharmacologie et Toxicologie, Université de Lausanne, Faculté de Médecine, Switzerland.
Pharm Acta Helv. 2000 Mar;74(2-3):173-9. doi: 10.1016/s0031-6865(99)00031-x.
In this chapter we summarize some aspects of the structure-functional relationship of the alpha 1a and alpha 1b-adrenergic receptor subtypes related to the receptor activation process as well as the effect of different alpha-blockers on the constitutive activity of the receptor. Molecular modeling of the alpha 1a and alpha 1b-adrenergic receptor subtypes and computational simulation of receptor dynamics were useful to interpret the experimental findings derived from site directed mutagenesis studies.
在本章中,我们总结了α1a和α1b肾上腺素能受体亚型的结构-功能关系的一些方面,这些方面与受体激活过程以及不同α阻滞剂对受体组成活性的影响有关。α1a和α1b肾上腺素能受体亚型的分子建模以及受体动力学的计算模拟有助于解释定点诱变研究得出的实验结果。