Rodnight R, Perrett C, Dosemeci A
Neurochem Res. 1986 Jul;11(7):1049-60. doi: 10.1007/BF00965593.
Endogenous protein phosphorylation patterns were compared in occluded and non-occluded cytosol fractions prepared from rat forebrain. The occluded fraction was taken as representative of synaptosomal cytosol. One- and two-dimensional autoradiographs revealed the presence in non-occluded cytosol of a substrate for cAMP- and Ca2+/calmodulin-dependent protein kinase activities of Mr 300kD, corresponding to phosphorylated microtubule-associated protein-2 (MAP-2); this protein was absent in occluded cytosol. In contrast, a major substrate for protein kinase C was observed exclusively in occluded cytosol after phosphorylation under basal conditions. However, after phosphorylation in the presence of exogenous lipids, approximately equal amounts of the 82kD substrate were detected in both fractions, suggesting that protein kinase C in the occluded fraction was present in a partially activated state. Other minor differences in phosphorylation patterns between the two fractions were observed.
对从大鼠前脑制备的封闭和未封闭胞质溶胶组分中的内源性蛋白质磷酸化模式进行了比较。封闭组分被视为突触体胞质溶胶的代表。一维和二维放射自显影片显示,在未封闭的胞质溶胶中存在一种分子量为300kD的cAMP和Ca2+/钙调蛋白依赖性蛋白激酶活性的底物,对应于磷酸化的微管相关蛋白-2(MAP-2);该蛋白在封闭的胞质溶胶中不存在。相反,在基础条件下磷酸化后,仅在封闭的胞质溶胶中观察到蛋白激酶C的主要底物。然而,在外源脂质存在下磷酸化后,在两个组分中检测到的82kD底物量大致相等,这表明封闭组分中的蛋白激酶C处于部分活化状态。观察到两个组分之间磷酸化模式的其他微小差异。