Jones T R, Sloman J C, Bell P A
Mol Cell Endocrinol. 1979 Jan;13(1):83-92. doi: 10.1016/0303-7207(79)90078-9.
Competitive steroid-binding studies were performed with intact rat thymus cells and with cytosol preparations at different temperatures using [1,2-3H]dexamethasone as the labelled ligand. Steroids lacking a 17 alpha-hydroxyl group, such as corticosterone, were better able to compete with [1,2-3H]dexamethasone for binding to glucocorticoid receptors at 0 degrees C than compounds containing a 17 alpha-hydroxyl substituent, such as cortisol. At 37 degrees C the reverse was true. This temperature-dependent change in relative affinities appeared to be unrelated to steroid metabolism or receptor activation, and to depend only on the thermodynamic parameters of the steroid--receptor interaction. Relative biological activities for different steroids agree more closely with the relative affinities determined at 37 degrees C than with those determined at lower temperatures.
使用[1,2-³H]地塞米松作为标记配体,在不同温度下对完整的大鼠胸腺细胞和胞质溶胶制剂进行了竞争性类固醇结合研究。缺乏17α-羟基的类固醇,如皮质酮,在0℃时比含有17α-羟基取代基的化合物,如皮质醇,更能与[1,2-³H]地塞米松竞争结合糖皮质激素受体。在37℃时则相反。这种相对亲和力的温度依赖性变化似乎与类固醇代谢或受体激活无关,仅取决于类固醇 - 受体相互作用的热力学参数。不同类固醇的相对生物活性与在37℃时测定的相对亲和力比与在较低温度下测定的相对亲和力更密切相关。