Richter M L, Patrie W J, McCarty R E
J Biol Chem. 1984 Jun 25;259(12):7371-3.
A simple and rapid method is described for releasing the epsilon subunit from chloroplast coupling factor 1 by treatment with 20% ethanol on an anion exchange column. The resulting epsilon subunit-deficient enzyme is a permanently active Ca2+-ATPase, but an inactive coupling factor. Recombination with the epsilon subunit returns the enzyme to the latent Ca2+-ATPase state and restores its ability to synthesize ATP when reconstituted with thylakoid membranes. The epsilon subunit is not required for binding coupling factor 1 to the membrane, but its presence is necessary to prevent the leak of protons through the hydrophobic portion of the coupling factor complex.
本文描述了一种简单快速的方法,即在阴离子交换柱上用20%乙醇处理,从叶绿体偶联因子1中释放ε亚基。由此产生的缺乏ε亚基的酶是一种永久活性的Ca2+ -ATP酶,但却是无活性的偶联因子。与ε亚基重组可使该酶恢复到潜在的Ca2+ -ATP酶状态,并在与类囊体膜重构时恢复其合成ATP的能力。ε亚基对于偶联因子1与膜的结合不是必需的,但其存在对于防止质子通过偶联因子复合物的疏水部分泄漏是必要的。