Traish A M, Müller R E, Wotiz H H
J Steroid Biochem. 1985 May;22(5):601-9. doi: 10.1016/0022-4731(85)90212-2.
This study shows that cytosolic androgen receptor of rat ventral prostate sediments at 10-11 S on conventional low salt sucrose density gradients (SDG), and at 4.6 S on high salt SDG, whether it is activated or not; inclusion of 10 mM Na2MoO4 in all buffers does not alter these sedimentation coefficients. In the presence of 50 mM Na2MoO4 non-activated and activated androgen receptors sediment in high salt SDG at 7-8 S and 4.6 S, respectively. Thus the presence of high concentrations of molybdate during centrifugation inhibits the KCl induced disaggregation of receptor into subunits. Similar effects are observed on Sephacryl-S200 gel filtration; in 50 mM MoO2-4 and 0.4 M KCl non-activated receptor has an estimated Stokes radius of 67 A; this value decreases to 52 A upon activation in the presence of proteolysis inhibitors; omission of molybdate during chromatography yielded 52 A and 27 A entities. Estimated mol. wts are 198,000 Daltons for the non-activated 67 A form and 98,000 Daltons for the activated 52 A receptor. Sodium molybdate (50 mM) prevents temperature (18 degrees C) and high ionic strength (0.4 M KCl) induced receptor activation. This inhibition was overcome by removing molybdate by centrifugal gel filtration, or by increasing the KCl concentration to 0.8 M. The inhibitory effects of molybdate on salt induced receptor disaggregation into activated subunits are no longer observed at pH greater than 7.4 or after chemical modification of sulfhydryl groups. Once androgen receptor has been disaggregated into its activated subunits the activated state is maintained even upon reassociation to 10-11 S aggregates in low salt. The relative concentrations of KCl and molybdate are critical; thus, 10 mM Na2MoO4/0.4 M KCl and 50 mM Na2MoO4/0.8-1.2 M KCl did not differentiate activated from non-activated androgen receptor based on their hydrodynamic properties. In the presence of 0.4 M KCl and 50 mM molybdate, however, the hydrodynamic properties of androgen receptor can be correlated with receptor activation.
本研究表明,大鼠腹侧前列腺的胞质雄激素受体在常规低盐蔗糖密度梯度(SDG)上于10 - 11 S沉降,在高盐SDG上于4.6 S沉降,无论其是否被激活;在所有缓冲液中加入10 mM Na2MoO4不会改变这些沉降系数。在50 mM Na2MoO4存在下,未激活和激活的雄激素受体在高盐SDG中分别于7 - 8 S和4.6 S沉降。因此,离心过程中高浓度钼酸盐的存在抑制了KCl诱导的受体解聚为亚基。在Sephacryl - S200凝胶过滤中观察到类似的效果;在50 mM MoO2-4和0.4 M KCl存在下,未激活的受体估计斯托克斯半径为67 Å;在蛋白水解抑制剂存在下激活后,该值降至52 Å;色谱过程中省略钼酸盐会产生52 Å和27 Å的实体。未激活的67 Å形式的估计分子量为198,000道尔顿,激活的52 Å受体的估计分子量为98,000道尔顿。钼酸钠(50 mM)可防止温度(18℃)和高离子强度(0.4 M KCl)诱导的受体激活。通过离心凝胶过滤去除钼酸盐或通过将KCl浓度提高到0.8 M可克服这种抑制作用。在pH大于7.4或巯基化学修饰后,不再观察到钼酸盐对盐诱导的受体解聚为激活亚基的抑制作用。一旦雄激素受体解聚为其激活的亚基,即使在低盐条件下重新聚合成10 - 11 S聚集体,激活状态仍会维持。KCl和钼酸盐的相对浓度至关重要;因此,10 mM Na2MoO4/0.4 M KCl和50 mM Na2MoO4/0.8 - 1.2 M KCl根据其流体动力学性质无法区分激活的和未激活的雄激素受体。然而,在0.4 M KCl和50 mM钼酸盐存在下,雄激素受体的流体动力学性质可与受体激活相关联。