Banerji A, Kalimi M
Steroids. 1981 Apr;37(4):409-21. doi: 10.1016/0039-128x(81)90043-x.
An exchange assay for the assessment of glucocorticoid binding sites both free and steroid bound, in rat liver cytosol has been developed. The procedure, which is straight forward and noncumbersome involves the utilization of two sulfhydryl interacting agents, p-hydroxymercuribenzoate and dithiothreitol. The former in low concentration dissociates the steroid from the glucocorticoid receptor complex in relatively short time. The latter regenerates, quite rapidly and with good yield, the glucocorticoid binding activity of the receptor treated with the mercurial compound. The high recovery (99%) of the hormone binding activity of the receptor may be due to the few steps involved in the procedure. The exchange assay when applied to a physiological experimental situation was found to be valid and gave a true measure of total receptor content in rat hepatic cytosolic preparations.
已开发出一种用于评估大鼠肝细胞溶胶中游离和类固醇结合的糖皮质激素结合位点的交换测定法。该方法简单直接且不繁琐,涉及使用两种巯基相互作用剂,对羟基汞苯甲酸和二硫苏糖醇。前者在低浓度下能在相对较短时间内使类固醇从糖皮质激素受体复合物中解离。后者能非常迅速且高产率地使经汞化合物处理的受体的糖皮质激素结合活性再生。受体激素结合活性的高回收率(99%)可能归因于该方法涉及的步骤较少。当将该交换测定法应用于生理实验情况时,发现其是有效的,并且能真实测量大鼠肝细胞溶胶制剂中的总受体含量。