Weinman E J, Dubinsky W P, Dinh Q, Steplock D, Shenolikar S
Department of Internal Medicine, University of Texas Medical School, Houston 77025.
J Membr Biol. 1989 Aug;109(3):233-41. doi: 10.1007/BF01870280.
The Na+-H+ exchanger from solubilized rabbit renal brush border membranes is inhibited by cAMP-dependent protein kinase (PKA) mediated protein phosphorylation. To characterize this inhibitory response and its sensitivity to limited proteolysis, the activity of the transporter was assayed after reconstitution of the proteins into artificial lipid vesicles. Limited trypsin digestion increased the basal rate of proton gradient-stimulated, amiloride-inhibitable sodium uptake in reconstituted proteoliposomes and blocked the inhibitory response to PKA-mediated protein phosphorylation. To determine if the inhibitory response to PKA-mediated protein phosphorylation could be restored to the trypsin-treated solubilized proteins, nontrypsinized solubilized brush border membrane proteins were separated by column chromatography. The addition of small molecular weight polypeptides, fractionated on Superose-12 FPLC (Ve = 0.7), to trypsinized solubilized brush border membrane proteins restored the inhibitory response to PKA-mediated protein phosphorylation. Similarly, the addition of the 0.1 M NaCl fraction from an anion exchange column, Mono Q-FPLC, also restored the inhibitory response to PKA. Both protein fractions contained a common 42-43 kDa protein which was preferentially phosphorylated by PKA. These results indicate that limited trypsin digestion dissociates the activity of the renal Na+-H+ exchanger from its regulation by PKA. It is suggested that trypsin cleaves an inhibitory component of the transporter and that this component is the site of PKA-mediated regulation. Phosphoprotein analysis of fractions that restored PKA regulation raises the possibility that a polypeptide of 42-43 kDa is involved in the inhibition of the renal Na+-H+ exchanger by PKA-mediated protein phosphorylation.
来自溶解的兔肾刷状缘膜的Na + -H +交换体受到cAMP依赖性蛋白激酶(PKA)介导的蛋白磷酸化的抑制。为了表征这种抑制反应及其对有限蛋白酶解的敏感性,在将蛋白质重组成人工脂质体后测定转运体的活性。有限的胰蛋白酶消化增加了重组蛋白脂质体中质子梯度刺激的、氨氯地平抑制的钠摄取的基础速率,并阻断了对PKA介导的蛋白磷酸化的抑制反应。为了确定对PKA介导的蛋白磷酸化的抑制反应是否可以恢复到经胰蛋白酶处理的溶解蛋白,通过柱色谱分离未用胰蛋白酶处理的溶解刷状缘膜蛋白。将在Superose-12 FPLC(Ve = 0.7)上分级分离的小分子量多肽添加到经胰蛋白酶处理的溶解刷状缘膜蛋白中,恢复了对PKA介导的蛋白磷酸化的抑制反应。同样,添加来自阴离子交换柱Mono Q-FPLC的0.1 M NaCl级分也恢复了对PKA的抑制反应。这两个蛋白级分都含有一种常见的42 - 43 kDa蛋白,该蛋白优先被PKA磷酸化。这些结果表明,有限的胰蛋白酶消化使肾Na + -H +交换体的活性与其受PKA的调节分离。有人提出,胰蛋白酶切割转运体的一个抑制成分,并且这个成分是PKA介导调节的位点。对恢复PKA调节的级分的磷蛋白分析增加了一种可能性,即42 - 43 kDa的多肽参与了PKA介导的蛋白磷酸化对肾Na + -H +交换体的抑制作用。