Scheer A, Cotecchia S
Institut de Pharmacologie et de Toxicologie Université de Lausanne, Switzerland.
J Recept Signal Transduct Res. 1997 Jan-May;17(1-3):57-73. doi: 10.3109/10799899709036594.
Mutations of G protein-coupled receptors can increase their constitutive (agonist-independent) activity. Some of these mutations have been artificially introduced by site-directed mutagenesis, others occur spontaneously in human diseases. The analysis of the constitutively active G protein-coupled receptors has provided important informations about the molecular mechanisms underlying receptor activation and drug action.
G蛋白偶联受体的突变可增加其组成性(不依赖激动剂)活性。其中一些突变是通过定点诱变人工引入的,另一些则在人类疾病中自发发生。对组成型活性G蛋白偶联受体的分析为受体激活和药物作用的分子机制提供了重要信息。