Department of Biology, University of California, Santa Cruz, Santa Cruz, California 95064.
Plant Physiol. 1989 Feb;89(2):391-5. doi: 10.1104/pp.89.2.391.
The vacuolar H(+)-ATPase of maize (Zea mays L.) root tip cells has been localized at the EM level using rabbit polyclonal antibodies to the 69 kilodalton subunit and protein A-colloidal gold. Intracellular gold particles were detected mainly on the tonoplast and Golgi membranes. Only about 27% of the vacuoles were labeled above background. The absence of gold particles on the majority of vacuoles suggests either that the tonoplast H(+)-ATPase is degraded during tissue preparation or that the small vacuoles of root tip cells are specialized with respect to H(+)-ATP ase activity. The pattern of gold particles on the labeled vacuoles ranged from uniform to patchy. Virtually all of the Golgi bodies were labeled by the antibody, but the particle densities were too low to determine whether the H(+)-ATPase was associated with specific regions, such as the trans-face. Cell wall-labeling was also observed which could be partially prevented by the inclusion of gelatin as a blocking agent. The immunocytochemical results confirm previous biochemical studies with isolated membrane fractions (A Chanson, L Taiz 1985 Plant Physiol 78: 232-240).
使用针对 69 千道尔顿亚基的兔多克隆抗体和蛋白 A-胶体金,在电镜水平对玉米(Zea mays L.)根尖细胞的液泡 H(+)-ATP 酶进行了定位。细胞内的金颗粒主要位于液泡膜和高尔基体膜上。只有约 27%的液泡被标记到背景以上。大多数液泡上没有金颗粒,这表明要么是在组织制备过程中液泡膜 H(+)-ATP 酶被降解,要么是根尖细胞的小液泡在 H(+)-ATP 酶活性方面具有特异性。标记的液泡上的金颗粒图案从均匀到斑片状不等。几乎所有的高尔基体都被抗体标记,但颗粒密度太低,无法确定 H(+)-ATP 酶是否与特定区域(如反式面)相关。还观察到细胞壁标记,通过包含明胶作为封闭剂可以部分防止这种标记。免疫细胞化学结果证实了以前对分离的膜部分进行的生化研究(A Chanson,L Taiz 1985 Plant Physiol 78: 232-240)。