Staehelin L A
J Cell Biol. 1976 Oct;71(1):136-58. doi: 10.1083/jcb.71.1.136.
Freeze-fracture and freeze-etch techniques have been employed to study the supramolecular structure of isolated spinach chloroplast membranes and to monitor structural changes associated with in vitro unstacking and restacking of these membranes. High-resolution particle size histograms prepared from the four fracture faces of normal chloroplast membranes reveal the presence of four distinct categories of intramembranous particles that are nonrandomly distributed between grana and stroma membranes. The large surface particles show a one to one relationship with the EF-face particles. Since the distribution of these particles between grana and stroma membranes coincides with the distribution of photosystem II (PS II) activity, it is argued that they could be structural equivalents of PS II complexes. An interpretative model depicting the structural relationship between all categories of particles is presented. Experimental unstacking of chloroplast membranes in low-salt medium for at least 45 min leads to a reorganization of the lamellae and to a concomitant intermixing of the different categories of membrane particles by means of translational movements in the plane of the membrane. In vitro restacking of such experimentally unstacked chloroplast membranes can be achieved by adding 2-20 mM MgCl2 or 100-200 mM NaCl to the membrane suspension. Membranes allowed to restack for at least 1 h at room temperature demonstrate a resegregation of the EF-face particles into the newly formed stacked membrane regions to yield a pattern and a size distribution nearly indistinguishable from the normally stacked controls. Restacking occurs in two steps: a rapid adhesion of adjoining stromal membrane surfaces with little particle movement, and a slower diffusion of additional large intramembranous particles into the stacked regions where they become trapped. Chlorophyll a:chlorophyll b ratios of membrane fraction obtained from normal, unstacked, and restacked membranes show that the particle movements are paralleled by movements of pigment molecules. The directed and reversible movements of membrane particles in isolated chloroplasts are compared with those reported for particles of plasma membranes.
冷冻断裂和冷冻蚀刻技术已被用于研究分离的菠菜叶绿体膜的超分子结构,并监测与这些膜的体外解堆叠和重新堆叠相关的结构变化。从正常叶绿体膜的四个断裂面制备的高分辨率颗粒大小直方图显示存在四类不同的膜内颗粒,它们在基粒和基质膜之间呈非随机分布。大的表面颗粒与EF面颗粒呈一一对应关系。由于这些颗粒在基粒和基质膜之间的分布与光系统II(PS II)活性的分布一致,因此有人认为它们可能是PS II复合物的结构等效物。本文提出了一个描述所有颗粒类别之间结构关系的解释性模型。在低盐介质中对叶绿体膜进行至少45分钟的实验性解堆叠会导致片层重新组织,并通过膜平面内的平移运动使不同类别的膜颗粒随之混合。通过向膜悬浮液中添加2 - 20 mM MgCl2或100 - 200 mM NaCl,可以实现这种实验性解堆叠的叶绿体膜的体外重新堆叠。在室温下允许重新堆叠至少1小时的膜显示EF面颗粒重新分离到新形成的堆叠膜区域,产生的模式和大小分布与正常堆叠的对照几乎无法区分。重新堆叠分两步进行:相邻基质膜表面的快速粘附,颗粒运动很少,以及额外的大膜内颗粒较慢地扩散到堆叠区域并被困在其中。从正常、解堆叠和重新堆叠的膜中获得的膜部分的叶绿素a:叶绿素b比率表明,颗粒运动与色素分子的运动平行。将分离的叶绿体中膜颗粒的定向和可逆运动与质膜颗粒的相关报道进行了比较。