Maruyama M
Brain Res. 1986 Apr 2;370(1):186-90. doi: 10.1016/0006-8993(86)91122-4.
Active substance P binding sites were solubilized from rat brain membranes by treatment with 0.125% sodium glycodeoxycholate and 1 M NaCl. About 50% of the binding activity in membrane-bound binding sites was recovered in the solubilized fraction after centrifugation at 105,000 g for 1 h. [3H]Substance P absorbed extensively to glass tubes and glass filters, but the absorption was greatly reduced by siliconizing glass tubes and preincubating glass filters in a solution containing poly-D-lysine and bovine serum albumin. [3H]Substance P was found to bind the solubilized receptors in a saturable fashion with a Bmax of 145 fmol/mg protein and a Kd of 4.6 nM, and these bindings were completely replaced by low concentrations of unlabeled substance P and physalaemin.
通过用0.125%甘氨脱氧胆酸钠和1 M氯化钠处理,从大鼠脑膜中溶解活性物质P结合位点。在105,000 g离心1小时后,膜结合结合位点中约50%的结合活性在溶解部分中得以恢复。[3H]物质P大量吸附于玻璃管和玻璃滤器,但通过硅化玻璃管以及在含有聚-D-赖氨酸和牛血清白蛋白的溶液中预孵育玻璃滤器,吸附作用可大大降低。发现[3H]物质P以饱和方式结合溶解的受体,Bmax为145 fmol/mg蛋白质,Kd为4.6 nM,并且这些结合可被低浓度的未标记物质P和physalaemin完全取代。