Omukai Y, Nohno T, Ikeda M, Watanabe S, Senoo T, Saito T, Hosokawa K
J Steroid Biochem. 1983 Aug;19(2):1055-9. doi: 10.1016/0022-4731(83)90397-7.
The effects of KSCN and other chaotropic salts on the androgen receptor in cytosol of Shionogi carcinoma 115 were studied by means of charcoal adsorption assay and sucrose gradient centrifugation. When KSCN or NaSCN was added to the [3H]-dihydrotestosterone-cytosol mixture at the final concentration of 0.5 M, the androgen binding to the cytosol receptor was considerably inhibited. The inhibition reached maximum within 5 h at 0 degrees C and was dependent on the kind of chaotropic anion added: the potency of inhibitory effect in descending order was KSCN greater than KI greater than KBr greater than KCl. The inhibition was not observed in the estradiol-receptor interaction with KSCN or NaSCN up to 0.5 M. When 0.5 M KSCN-treated androgen-cytosol mixture was subjected to gel filtration or (NH4)2SO4 fractionation to remove the salt, a partial recovery (30-40%) in specific binding activity was observed. The binding activity of androgen receptor was unaffected by a treatment with KSCN up to 0.1 M and the androgen-receptor complex sedimented in a 5S form in 0.1-0.3 M KSCN, 0.5 M KCl or 0.5 M KBr. These results suggest that the binding activity of androgen receptor is more susceptible than that of estrogen receptor to chaotropic salts which cause impairment in intramolecular hydrophobic interactions.
通过活性炭吸附测定法和蔗糖梯度离心法,研究了硫氰酸钾(KSCN)和其他离液盐对狮王癌115细胞溶质中雄激素受体的影响。当将KSCN或硫氰酸钠(NaSCN)以终浓度0.5 M添加到[3H]-二氢睾酮-细胞溶质混合物中时,雄激素与细胞溶质受体的结合受到显著抑制。在0℃下,这种抑制作用在5小时内达到最大值,并且取决于所添加的离液阴离子的种类:抑制作用的效力从高到低依次为KSCN>KI>KBr>KCl。在高达0.5 M的KSCN或NaSCN存在下,雌二醇-受体相互作用未观察到抑制作用。当对经0.5 M KSCN处理的雄激素-细胞溶质混合物进行凝胶过滤或硫酸铵分级分离以去除盐分后,观察到特异性结合活性有部分恢复(30%-40%)。高达0.1 M的KSCN处理对雄激素受体的结合活性没有影响,并且在0.1-0.3 M KSCN、0.5 M KCl或0.5 M KBr中,雄激素-受体复合物以5S形式沉淀。这些结果表明,雄激素受体的结合活性比雌激素受体对导致分子内疏水相互作用受损的离液盐更敏感。