Yamamoto Misaki, Unzai Satoru, Saijo Shinya, Ito Kazuki, Mizutani Kenji, Suno-Ikeda Chiyo, Yabuki-Miyata Yukako, Terada Takaho, Toyama Mitsutoshi, Shirouzu Mikako, Kobayashi Takuya, Kakinuma Yoshimi, Yamato Ichiro, Yokoyama Shigeyuki, Iwata So, Murata Takeshi
Department of Biological Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda-shi, Chiba 278-8510, Japan.
J Biol Chem. 2008 Jul 11;283(28):19422-31. doi: 10.1074/jbc.M801772200. Epub 2008 May 6.
The vacuolar ATPase (V-ATPase) is composed of a soluble catalytic domain and an integral membrane domain connected by a central stalk and a few peripheral stalks. The number and arrangement of the peripheral stalk subunits remain controversial. The peripheral stalk of Na+-translocating V-ATPase from Enterococcus hirae is likely to be composed of NtpE and NtpF (corresponding to subunit G of eukaryotic V-ATPase) subunits together with the N-terminal hydrophilic domain of NtpI (corresponding to subunit a of eukaryotic V-ATPase). Here we purified NtpE, NtpF, and the N-terminal hydrophilic domain of NtpI (NtpI(Nterm)) as separate recombinant His-tagged proteins and examined interactions between these three subunits by pulldown assay using one tagged subunit, CD spectroscopy, surface plasmon resonance, and analytical ultracentrifugation. NtpI(Nterm) directly bound NtpF, but not NtpE. NtpE bound NtpF tightly. NtpI(Nterm) bound the NtpE-F complex stronger than NtpF only, suggesting that NtpE increases the binding affinity between NtpI(Nterm) and NtpF. Purified NtpE-F-I(Nterm) complex appeared to be monodisperse, and the molecular masses estimated from analytical ultracentrifugation and small-angle x-ray scattering (SAXS) indicated that the ternary complex is formed with a 1:1:1 stoichiometry. A low resolution structure model of the complex produced from the SAXS data showed an elongated "L" shape.
液泡型ATP酶(V-ATP酶)由一个可溶性催化结构域和一个通过中央柄及一些外周柄相连的整合膜结构域组成。外周柄亚基的数量和排列仍存在争议。来自平肠球菌的Na⁺转运V-ATP酶的外周柄可能由NtpE和NtpF(对应于真核生物V-ATP酶的G亚基)亚基以及NtpI的N端亲水区(对应于真核生物V-ATP酶的a亚基)组成。在这里,我们将NtpE、NtpF以及NtpI的N端亲水区(NtpI(Nterm))作为单独的重组His标签蛋白进行纯化,并通过使用一种标签亚基的下拉试验、圆二色光谱、表面等离子体共振和分析超速离心来检测这三个亚基之间的相互作用。NtpI(Nterm)直接结合NtpF,但不结合NtpE。NtpE与NtpF紧密结合。NtpI(Nterm)结合NtpE-F复合物比仅结合NtpF更强,这表明NtpE增加了NtpI(Nterm)与NtpF之间的结合亲和力。纯化的NtpE-F-I(Nterm)复合物似乎是单分散的,通过分析超速离心和小角X射线散射(SAXS)估计的分子量表明三元复合物以1:1:1的化学计量比形成。由SAXS数据生成的复合物的低分辨率结构模型显示出一个细长的“L”形。