Johnson D E, Bauer G E, Williams F G, Dixit P K
Metabolism. 1984 Jan;33(1):8-14. doi: 10.1016/0026-0495(84)90155-0.
Preliminary studies were conducted to develop a cell-free system for insulin biosynthesis using the streptozotocin-nicotinamide--induced rat islet adenoma. Radiolabeled proteins, migrating on steric exclusion chromatography and SDS-gel electrophoresis in the region of insulin and proinsulin, were synthesized in a system prepared from the tumor 800 X g supernatant fraction, rat liver cytosol, and appropriate energy substrates. The proteins were not synthesized by a rat liver cell-free system, and synthesis could be substantially inhibited by the addition of cycloheximide. In addition, it could be shown that the islet proteins were not the products of residual intact cells within the system, nor were they an artifact due to nonspecific binding of [3H]-L-leucine to pre-existing insulin and proinsulin. The radiolabeled material eluting with insulin on steric exclusion chromatography was identified as [3H]-insulin by immunoaffinity column chromatography.
利用链脲佐菌素 - 烟酰胺诱导的大鼠胰岛腺瘤开展了初步研究,以开发一种用于胰岛素生物合成的无细胞系统。在由肿瘤800X g上清液组分、大鼠肝脏胞质溶胶和合适的能量底物制备的系统中,合成了在胰岛素和胰岛素原区域通过空间排阻色谱法和SDS凝胶电泳迁移的放射性标记蛋白。这些蛋白不是由大鼠无细胞肝脏系统合成的,并且加入环己酰亚胺可显著抑制其合成。此外,可以证明胰岛蛋白不是系统内残留完整细胞的产物,也不是由于[3H]-L-亮氨酸与预先存在的胰岛素和胰岛素原非特异性结合而产生的假象。通过免疫亲和柱色谱法将在空间排阻色谱中与胰岛素一起洗脱的放射性标记物质鉴定为[3H]-胰岛素。