Hinshaw J E, Miller K R
Division of Biology and Medicine, Brown University, Providence, Rhode Island 02912.
J Cell Biol. 1989 Oct;109(4 Pt 1):1725-31. doi: 10.1083/jcb.109.4.1725.
The photosynthetic membranes of green plants are organized into stacked regions interconnected by nonstacked regions that have been shown to be biochemically and structurally distinct. Because the stacking process occludes the surfaces of appressed membranes, it has been impossible to conduct structural or biochemical studies of the outer surfaces of the photosynthetic membrane in regions of membrane stacking. Although stacking is mediated at this surface, it has not been possible to determine whether membrane components implicated in the stacking process, including a major light-harvesting complex (LHC-II), are in fact exposed at the membrane surface. We have been able to expose this surface for study in the electron microscope and directly label it with antibodies to determine protein exposure. The appearance of the newly exposed outer stacked surface highlights the extreme lateral heterogeneity of the photosynthetic membrane. The surface is smooth in contrast to the neighboring nonstacked surface that is covered with distinct particles. Although some investigators have suggested the existence of a cytochrome b6/f-rich boundary region between stacked and nonstacked membranes, our results provide no structural support for this concept. To explore the biochemical nature of the occluded membrane surface, we have used an mAb against the amino terminal region of the LHC-II. This mAb clearly labels the newly exposed outer stacked surface but does not label the inner surface or the outer nonstacked surface. These experimental results confirm the presence of the amino terminal region of this complex at the outer surface of the membrane in stacked regions, and also show that this complex is largely absent from nonstacked membranes.
绿色植物的光合膜被组织成堆叠区域,这些堆叠区域通过未堆叠区域相互连接,已证明这些未堆叠区域在生化和结构上是不同的。由于堆叠过程会封闭紧密排列膜的表面,因此无法对光合膜堆叠区域的外表面进行结构或生化研究。尽管堆叠是在这个表面介导的,但无法确定参与堆叠过程的膜成分,包括主要的光捕获复合物(LHC-II),是否实际上暴露在膜表面。我们能够将这个表面暴露出来用于电子显微镜研究,并直接用抗体标记它以确定蛋白质的暴露情况。新暴露的堆叠外表面的外观突出了光合膜极端的横向异质性。与覆盖着不同颗粒的相邻未堆叠表面相比,这个表面是光滑的。尽管一些研究人员提出在堆叠膜和未堆叠膜之间存在富含细胞色素b6/f的边界区域,但我们的结果没有为这一概念提供结构支持。为了探索被封闭的膜表面的生化性质,我们使用了一种针对LHC-II氨基末端区域的单克隆抗体。这种单克隆抗体清楚地标记了新暴露的堆叠外表面,但没有标记内表面或未堆叠外表面。这些实验结果证实了该复合物的氨基末端区域在堆叠区域膜的外表面存在,并且还表明该复合物在未堆叠膜中基本不存在。