Staehelin M, Hertel C
J Recept Res. 1983;3(1-2):35-43. doi: 10.3109/10799898309041921.
[3H]CGP-12177, in contrast to lipophilic ligands like [3H]Dihydroalprenolol, shows very little non-specific binding to intact cells. It also differs from lipophilic ligands in that it can be completely displaced from the receptors on intact cells by isoproterenol. Furthermore, binding sites for this ligand disappear rapidly upon exposure of cells to agonists. These binding sites reappear rapidly upon removal of the agonist, if any possible interaction with residual traces of the agonist are prevented. These results indicate that [3H]CGP-12177 binds only to cell surface receptors and that agonist causes a rapid and reversible shift of receptors from the cell surface to the interior of the cell.
与亲脂性配体如[³H]二氢阿普洛尔不同,[³H]CGP - 12177与完整细胞的非特异性结合非常少。它也与亲脂性配体不同,因为异丙肾上腺素能将其从完整细胞的受体上完全置换下来。此外,细胞暴露于激动剂后,该配体的结合位点会迅速消失。如果防止与激动剂残留痕迹的任何可能相互作用,去除激动剂后这些结合位点会迅速重新出现。这些结果表明,[³H]CGP - 12177仅与细胞表面受体结合,并且激动剂会导致受体从细胞表面快速且可逆地转移到细胞内部。