Weirich R T, McNabb F M
Gen Comp Endocrinol. 1984 Jan;53(1):90-9. doi: 10.1016/0016-6480(84)90228-4.
Binding studies were conducted using in vitro-labeled quail liver nuclei to identify and characterize receptors for L-triiodothyronine (T3). Saturation binding experiments were analyzed by Scatchard analysis and indicated a single class of high-affinity, limited-capacity T3 binding sites. These receptors exhibited binding specificity as demonstrated by competition experiments between labeled T3 and unlabeled thyroid hormones or hormone analogs. Binding specificity was virtually identical in quail and rat liver nuclei. Thus, apparent differences between mammals and birds, in regard to the biological potency of T4 versus T3, are not apparent at the level of the nuclear T3 receptor.
使用体外标记的鹌鹑肝细胞核进行结合研究,以鉴定和表征L-三碘甲状腺原氨酸(T3)的受体。通过Scatchard分析对饱和结合实验进行分析,结果表明存在一类单一的高亲和力、有限容量的T3结合位点。如标记的T3与未标记的甲状腺激素或激素类似物之间的竞争实验所示,这些受体表现出结合特异性。鹌鹑和大鼠肝细胞核中的结合特异性几乎相同。因此,在核T3受体水平上,哺乳动物和鸟类在T4与T3的生物学效力方面的明显差异并不明显。