Winder S J, Pato M D, Walsh M P
MRC Group in Signal Transduction, Faculty of Medicine, University of Calgary, Alberta, Canada.
Biochem J. 1992 Aug 15;286 ( Pt 1)(Pt 1):197-203. doi: 10.1042/bj2860197.
Calponin, a thin-filament protein of smooth muscle, has been implicated in the regulation of smooth-muscle contraction, since in vitro the isolated protein inhibits the actin-activated myosin MgATPase. This inhibitory effect, and the ability of calponin to bind to actin, is lost after its phosphorylation by protein kinase C or Ca2+/calmodulin-dependent protein kinase II [Winder & Walsh (1990) J. Biol. Chem. 265, 10148-10155]. If this phosphorylation reaction is of physiological significance, there must be a protein phosphatase in smooth muscle capable of dephosphorylating calponin and restoring its inhibitory effect on the actomyosin MgATPase. We demonstrate here the presence, in chicken gizzard smooth muscle, of a single major phosphatase activity directed towards calponin. This phosphatase was purified from the soluble fraction of chicken gizzard by (NH4)2SO4 fractionation and sequential chromatography on Sephacryl S-300, DEAE-Sephacel, omega-amino-octyl-agarose and thiophosphorylated myosin 20 kDa light-chain-Sepharose columns. The purified phosphatase contained three polypeptide chains of 60, 55 and 38 kDa which were shown to be identical with the subunits of SMP-I, a smooth-muscle phosphatase capable of dephosphorylating the isolated 20 kDa light chain of myosin but not intact myosin [Pato & Adelstein (1983) J. Biol. Chem. 258, 7047-7054]. Consistent with its identity with SMP-I, calponin phosphatase was classified as a type-2A protein phosphatase. Of several potential phosphoprotein substrates examined, calponin proved to be kinetically the best, suggesting that calponin may be a physiological substrate for this phosphatase. Finally, dephosphorylation of calponin which had been phosphorylated by protein kinase C restored completely its ability to inhibit the actin-activated MgATPase of smooth-muscle myosin. These observations support the hypothesis that calponin plays a role in regulating the contractile state of smooth muscle and that this function in turn is controlled by phosphorylation-dephosphorylation.
钙调蛋白是平滑肌的一种细肌丝蛋白,它与平滑肌收缩的调节有关,因为在体外,分离出的该蛋白可抑制肌动蛋白激活的肌球蛋白MgATP酶。在被蛋白激酶C或Ca2+/钙调蛋白依赖性蛋白激酶II磷酸化后,这种抑制作用以及钙调蛋白与肌动蛋白结合的能力就会丧失[温德和沃尔什(1990年)《生物化学杂志》265卷,第10148 - 10155页]。如果这种磷酸化反应具有生理意义,那么平滑肌中必定存在一种蛋白磷酸酶,它能够使钙调蛋白去磷酸化并恢复其对肌动球蛋白MgATP酶的抑制作用。我们在此证明,鸡胗平滑肌中存在一种针对钙调蛋白的主要磷酸酶活性。这种磷酸酶通过硫酸铵分级分离以及在Sephacryl S - 300、DEAE - Sephacel、ω - 氨基辛基琼脂糖和硫代磷酸化肌球蛋白20 kDa轻链琼脂糖柱上的连续层析,从鸡胗的可溶部分中纯化得到。纯化后的磷酸酶含有三条分别为60 kDa、55 kDa和38 kDa的多肽链,已证明它们与SMP - I的亚基相同,SMP - I是一种平滑肌磷酸酶,能够使分离出的肌球蛋白20 kDa轻链去磷酸化,但不能使完整的肌球蛋白去磷酸化[帕托和阿德尔斯坦(1983年)《生物化学杂志》258卷,第7047 - 7054页]。与其与SMP - I的一致性相符,钙调蛋白磷酸酶被归类为2A型蛋白磷酸酶。在检测的几种潜在磷蛋白底物中,钙调蛋白在动力学上被证明是最佳底物,这表明钙调蛋白可能是这种磷酸酶的生理底物。最后,被蛋白激酶C磷酸化的钙调蛋白去磷酸化后,完全恢复了其抑制平滑肌肌球蛋白肌动蛋白激活的MgATP酶的能力。这些观察结果支持了这样一种假说,即钙调蛋白在调节平滑肌收缩状态中起作用,而这种功能反过来又受磷酸化 - 去磷酸化控制。