大豆下胚轴可溶性蛋白中钙激活的蛋白激酶

大豆（Ｇｌｙｃｉｎｅ ｍ ａｘ Ｌ．） 下胚轴可溶性蛋白提取液进行自磷酸化，以ＳＤＳ－ＰＡＧＥ电泳分析其标记产物时发现，当有较高浓度的Ｃａ２＋ 存在于反应液中时，有一条１８ ｋＤ蛋白带被高强度标记，同时也可观察到另一条标记强度不高的６７ ｋＤ蛋白带． 当反应时间延长到１５ 或３０ｍ ｉｎ 时，它们的标记强度都逐渐减弱，最终从放射自显影底片上消失；在反应液中加入钙螯合剂ＥＧＴＡ 时，则只有６７ ｋＤ 被高强度标记；在磷酸化反应过程中加入非标记ＡＴＰ，蛋白中的３２Ｐ逐渐被非标记磷取代，表明反应体系处于磷酸化－脱磷酸化的平衡过程中，并有结果显示这一过程是钙依赖性的． 组蛋白Ｈ１ 可以使反应进程加快，表明提取液中的蛋白激酶可以利用它作为底物． 综合结果表明，１８ ｋＤ和６７ ｋＤ蛋白可能是具有自磷酸化能力且对Ｃａ２＋ 敏感的蛋白激酶，它们对Ｃａ２＋ 的不同反应，使得钙信号的传递更具可控性

Ca 2 ACTIVATED PROTEIN KINASES IN HYPOCOTYL OF SOYBEAN(GLYCINE MAX L.)

The soluble protein extract of soybean hypocotyl was autophosphorylated,the labeling products were analyzed by SDS PAGE. A 18 kD protein band was intensely labeled when a relatively high concentration of calcium was present, meanwhile a weakly labeled 67 kD protein band was also observed. When the reaction time was prolonged to 15 or 30 min, the labeling intensity of them was weakened gradually and the labeled bands disappeared eventually from the autoradiograph. If the calcium chelater EGTA was added into the reaction system, only 67 kD was phosphorylated with high intensity.When non labeled ATP was added during the reaction process, 32 P in the labeled proteins could be substituted gradually by Pi. This indicated that the reaction system was in a dynamic equilibrium of phosphorylation dephosphorylation. There were also data inferred that it was a calcium dependent process. Histon H1 could speed up the phosphorylation, suggesting that it was a suitable substrate for protein kinases in the extract. Findings support that 18 kD and 67 kD protein may be Ca 2 sensitive protein kinases that can be autophosphorylated. Their different responses to Ca 2 may make the calcium signal transduction controllable.