Fanchenko N D, Minima L S, Shchedrina R N, Sturchak S V, Pivnitskiĭ K K
Biull Eksp Biol Med. 1978 Apr;85(4):467-70.
Physico-chemical parameters of estradiol-receptor interaction in guinea pig uterine cytosol (velocity constants of association and dissociation, half-life time of estradiol-receptor complex, and the value of free energy change) were studied. The number of receptor sites per cell was calculated. It was shown that under conditions of different degree of approximation to the equilibrium, the affinity percentage in the system under study remained unchanged for the majority of steroids, this pointing to the achievement of equilibrium in these cases. The steroid affinity to the analyzed R-system depended on presence of intact 3- and 17beta-hydroxils with somewhat greater significance of 3-(phenolic) hydroxil of steroid molecule.
研究了豚鼠子宫胞质溶胶中雌二醇 - 受体相互作用的物理化学参数(结合和解离的速度常数、雌二醇 - 受体复合物的半衰期以及自由能变化值)。计算了每个细胞的受体位点数量。结果表明,在不同程度接近平衡的条件下,所研究系统中大多数类固醇的亲和力百分比保持不变,这表明在这些情况下达到了平衡。类固醇对分析的R - 系统的亲和力取决于完整的3 - 和17β - 羟基的存在,类固醇分子的3 - (酚)羟基的意义稍大一些。