Hashimoto Y, Soderling T R
Howard Hughes Medical Institute, Nashville, Tennessee.
J Biol Chem. 1989 Oct 5;264(28):16524-9.
The site in calcineurin, the Ca2+/calmodulin (CaM)-dependent protein phosphatase, which is phosphorylated by Ca2+/CaM-dependent protein kinase II (CaM-kinase II) has been identified. Analyses of 32P release from tryptic and cyanogen bromide peptides derived from [32P]calcineurin plus direct sequence determination established the site as -Arg-Val-Phe-Ser(PO4)-Val-Leu-Arg-, which conformed to the consensus phosphorylation sequence for CaM-kinase II (Arg-X-X-Ser/Thr-). This phosphorylation site is located at the C-terminal boundary of the putative CaM-binding domain in calcinerin (Kincaid, R. L., Nightingale, M. S., and Martin, B. M. (1988) Proc. Natl. Acad. Sci. U. S. A. 85, 8983-8987), thereby accounting for the observed inhibition of this phosphorylation when Ca2+/CaM is bound to calcineurin. Since the phosphorylation site sequence also contains elements of the specificity determinants for Ca2+/phospholipid-dependent protein kinase (protein kinase C) (basic residues both N-terminal and C-terminal to Ser/Thr), we tested calcineurin as a substrate for protein kinase C. Protein kinase C catalyzed rapid stoichiometric phosphorylation, and the characteristics of the reaction were the same as with CaM-kinase II: 1) the phosphorylation was blocked by binding of Ca2+/CaM to calcineurin; 2) phosphorylation partially inactivated calcineurin by increasing the Km (from 9.9 +/- 1.1 to 17.5 +/- 1.1 microM 32P-labeled myosin light chain); and 3) [32P]calcineurin exhibited very slow autodephosphorylation but was rapidly dephosphorylated by protein phosphatase IIA. Tryptic and thermolytic 32P-peptide mapping and sequential phosphoamino acid sequence analysis confirmed that protein kinase C and CaM-kinase II phosphorylated the same site.
已确定钙调神经磷酸酶(一种Ca2+/钙调蛋白(CaM)依赖性蛋白磷酸酶)中被Ca2+/CaM依赖性蛋白激酶II(CaM激酶II)磷酸化的位点。对源自[32P]钙调神经磷酸酶的胰蛋白酶和溴化氰肽的32P释放进行分析,并结合直接序列测定,确定该位点为-Arg-Val-Phe-Ser(PO4)-Val-Leu-Arg-,它符合CaM激酶II的共有磷酸化序列(Arg-X-X-Ser/Thr-)。该磷酸化位点位于钙调神经磷酸酶中假定的CaM结合结构域的C末端边界(金凯德,R.L.,南丁格尔,M.S.,和马丁,B.M.(1988年)美国国家科学院院刊85,8983 - 8987),因此解释了当Ca2+/CaM与钙调神经磷酸酶结合时观察到的这种磷酸化的抑制现象。由于磷酸化位点序列还包含Ca2+/磷脂依赖性蛋白激酶(蛋白激酶C)特异性决定因素的元件(Ser/Thr的N末端和C末端均为碱性残基),我们测试了钙调神经磷酸酶作为蛋白激酶C的底物。蛋白激酶C催化快速的化学计量磷酸化,并且反应特性与CaM激酶II相同:1)Ca2+/CaM与钙调神经磷酸酶的结合阻断了磷酸化;2)磷酸化通过增加Km(从9.9±1.1到17.5±1.1 microM 32P标记的肌球蛋白轻链)使钙调神经磷酸酶部分失活;3)[32P]钙调神经磷酸酶表现出非常缓慢的自身去磷酸化,但被蛋白磷酸酶IIA迅速去磷酸化。胰蛋白酶和热解32P肽图谱分析以及连续的磷酸氨基酸序列分析证实蛋白激酶C和CaM激酶II磷酸化的是同一位点。