Bowman B J, Berenski C J, Jung C Y
J Biol Chem. 1985 Jul 25;260(15):8726-30.
Using radiation inactivation, we have measured the size of the H+-ATPase in Neurospora crassa plasma membranes. Membranes were exposed to either high energy electrons from a Van de Graaff generator or to gamma irradiation from 60Co. Both forms of radiation caused an exponential loss of ATPase activity in parallel with the physical destruction of the Mr = 104,000 polypeptide of which this enzyme is composed. By applying target theory, the size of the H+-ATPase in situ was found to be approximately 2.3 X 10(5) daltons. We also used radiation inactivation to measure the size of the Ca2+-ATPase of sarcoplasmic reticulum and got a value of approximately 2.4 X 10(5) daltons, in agreement with previous reports. By irradiating a mixture of Neurospora plasma membranes and rabbit sarcoplasmic reticulum, we directly compared the sizes of these two ATPases and found them to be essentially the same. We conclude that both H+-ATPase and Ca2+-ATPase are oligomeric enzymes, most likely composed of two approximately 100,000-dalton polypeptides.
我们运用辐射失活法测定了粗糙脉孢菌质膜中H⁺-ATP酶的大小。将膜暴露于范德格拉夫加速器产生的高能电子或⁶⁰Co的γ辐射下。两种辐射形式均导致ATP酶活性呈指数下降,同时该酶所由组成的分子量为104,000的多肽也遭受物理破坏。通过应用靶理论,发现原位H⁺-ATP酶的大小约为2.3×10⁵道尔顿。我们还运用辐射失活法测定了肌浆网Ca²⁺-ATP酶的大小,得到的值约为2.4×10⁵道尔顿,这与先前的报道一致。通过辐照粗糙脉孢菌质膜和兔肌浆网的混合物,我们直接比较了这两种ATP酶的大小,发现它们基本相同。我们得出结论,H⁺-ATP酶和Ca²⁺-ATP酶均为寡聚酶,很可能由两条分子量约为100,000道尔顿的多肽组成。