Jahn T, Fuglsang A T, Olsson A, Brüntrup I M, Collinge D B, Volkmann D, Sommarin M, Palmgren M G, Larsson C
Department of Plant Biochemistry, Lund University, Sweden.
Plant Cell. 1997 Oct;9(10):1805-14. doi: 10.1105/tpc.9.10.1805.
Accumulating evidence suggests that 14-3-3 proteins are involved in the regulation of plant plasma membrane H(+)-ATPase activity. However, it is not known whether the 14-3-3 protein interacts directly or indirectly with the H(+)-ATPase. In this study, detergent-solubilized plasma membrane H(+)-ATPase isolated from fusicoccin-treated maize shoots was copurified with the 14-3-3 protein (as determined by protein gel blotting), and the H(+)-ATPase was recovered in an activated state. In the absence of fusicoccin treatment, H(+)-ATPase and the 14-3-3 protein were well separated, and the H(+)-ATPase was recovered in a nonactivated form. Trypsin treatment removed the 10-kD C-terminal region from the H(+)-ATPase as well as the 14-3-3 protein. Using the yeast two-hybrid system, we could show a direct interaction between Arabidopsis 14-3-3 GF14-phi and the last 98 C-terminal amino acids of the Arabidopsis AHA2 plasma membrane H(+)-ATPase. We propose that the 14-3-3 protein is a natural ligand of the plasma membrane H(+)-ATPase, regulating proton pumping by displacing the C-terminal autoinhibitory domain of the H(+)-ATPase.
越来越多的证据表明,14-3-3蛋白参与植物质膜H(+) -ATP酶活性的调节。然而,尚不清楚14-3-3蛋白是直接还是间接与H(+) -ATP酶相互作用。在本研究中,从经壳梭孢菌素处理的玉米芽中分离出的经去污剂增溶的质膜H(+) -ATP酶与14-3-3蛋白共纯化(通过蛋白质凝胶印迹法测定),并且H(+) -ATP酶以活化状态回收。在没有壳梭孢菌素处理的情况下,H(+) -ATP酶和14-3-3蛋白被很好地分离,并且H(+) -ATP酶以非活化形式回收。胰蛋白酶处理从H(+) -ATP酶以及14-3-3蛋白中去除了10-kD的C末端区域。使用酵母双杂交系统,我们可以证明拟南芥14-3-3 GF14-phi与拟南芥AHA2质膜H(+) -ATP酶的最后98个C末端氨基酸之间存在直接相互作用。我们提出,14-3-3蛋白是质膜H(+) -ATP酶的天然配体,通过取代H(+) -ATP酶的C末端自抑制结构域来调节质子泵浦。