Department of Biochemistry, University of Georgia, Athens, Georgia 30602.
Plant Physiol. 1987 Apr;83(4):830-7. doi: 10.1104/pp.83.4.830.
A calcium-dependent protein kinase activity from suspension-cultured soybean cells (Glycine max L. Wayne) was shown to be dependent on calcium but not calmodulin. The concentrations of free calcium required for half-maximal histone H1 phosphorylation and autophosphorylation were similar ( approximately 2 micromolar). The protein kinase activity was stimulated 100-fold by >/=10 micromolar-free calcium. When exogenous soybean or bovine brain calmodulin was added in high concentration (1 micromolar) to the purified kinase, calcium-dependent and -independent activities were weakly stimulated (</=2-fold). Bovine serum albumin had a similar effect on both activities. The kinase was separated from a small amount of contaminating calmodulin by sodium dodecyl sulfate polyacrylamide gel electrophoresis. After renaturation the protein kinase autophosphorylated and phosphorylated histone H1 in a calcium-dependent manner. Following electroblotting onto nitrocellulose, the kinase bound (45)Ca(2+) in the presence of KCl and MgCl(2), which indicates that the kinase itself is a high-affinity calcium-binding protein. Also, the mobility of one of two kinase bands in SDS gels was dependent on the presence of calcium. Autophosphorylation of the calmodulin-free kinase was inhibited by the calmodulin-binding compound N-(6-aminohexyl)-5-chloro-1-naphthalene sulfonamide (W-7), showing that the inhibition of activity by W-7 is independent of calmodulin. These results show that soybean calcium-dependent protein kinase represents a new class of protein kinase which requires calcium but not calmodulin for activity.
从悬浮培养的大豆细胞(Glycine max L. Wayne)中分离出一种依赖钙但不依赖钙调蛋白的钙依赖性蛋白激酶活性。半最大组蛋白 H1 磷酸化和自磷酸化所需的游离钙浓度相似(约 2 微摩尔)。蛋白激酶活性在 >/=10 微摩尔游离钙的刺激下增加了 100 倍。当外源性大豆或牛脑钙调蛋白以高浓度(1 微摩尔)添加到纯化的激酶中时,钙依赖性和非依赖性活性被弱刺激(</=2 倍)。牛血清白蛋白对这两种活性都有类似的影响。激酶通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳从少量污染的钙调蛋白中分离出来。在复性后,蛋白激酶以钙依赖性方式自磷酸化并磷酸化组蛋白 H1。经电转移至硝酸纤维素后,激酶在 KCl 和 MgCl2 的存在下结合(45)Ca(2+),这表明激酶本身是一种高亲和力的钙结合蛋白。此外,SDS 凝胶中两条激酶带之一的迁移率取决于钙的存在。无钙调蛋白的激酶的自磷酸化被钙调蛋白结合化合物 N-(6-氨基己基)-5-氯-1-萘磺酰胺(W-7)抑制,表明 W-7 对活性的抑制与钙调蛋白无关。这些结果表明,大豆钙依赖性蛋白激酶代表了一种新的蛋白激酶类,其活性需要钙而不需要钙调蛋白。