Kanigür G, Kan B, Tiryaki D, Bermek E
Biochem Biophys Res Commun. 1983 Nov 30;117(1):135-40. doi: 10.1016/0006-291x(83)91551-6.
The treatment of reticulocyte post-ribosomal supernatant containing ribosome wash with high pO2 or glutathione disulfide resulted in the activation of an inhibitor of protein synthesis of approximately 23,000-Mr as implicated by its elution from Sephadex G-100. This inhibitor could also be directly activated by exposure of the approximately 23,000-Mr fractions of the control eluate to high pO2 or glutathione disulfide. The high pO2-dependent activation of the inhibitor was blocked by the presence of glucose-6-phosphate or cAMP (2 mM). The inhibitor was stable (and activable) during a 5 minute incubation at 80 degrees C. The analysis by sodium dodecyl sulfate-polyacrylamide gel electrophoresis of the G-100 (approximately 23,000-Mr) fractions treated with [14C]N-ethylmaleimide revealed the abolishment of the label in a approximately 23,000-Mr protein band in parallel to high pO2-dependent inhibitor activation.
用高氧分压或二硫化谷胱甘肽处理含有核糖体洗涤液的网织红细胞核糖体后上清液,导致一种分子量约为23,000的蛋白质合成抑制剂被激活,这可从其在Sephadex G - 100上的洗脱情况看出。将对照洗脱液中分子量约为23,000的组分暴露于高氧分压或二硫化谷胱甘肽也可直接激活该抑制剂。葡萄糖 - 6 - 磷酸或环磷酸腺苷(2 mM)的存在可阻断该抑制剂的高氧分压依赖性激活。该抑制剂在80摄氏度孵育5分钟期间稳定(且可激活)。用[14C]N - 乙基马来酰亚胺处理G - 100(分子量约为23,000)组分后进行的十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳分析显示,与高氧分压依赖性抑制剂激活同时,分子量约为23,000的蛋白条带中的标记消失。