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首页> 外文期刊>Journal of cell biology >Localization of light-harvesting complex II to the occluded surfaces of photosynthetic membranes.
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Localization of light-harvesting complex II to the occluded surfaces of photosynthetic membranes.

机译:光捕获复合物II定位到光合膜的被遮挡表面。

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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.
机译:绿色植物的光合膜被组织成由非堆叠区域互连的堆叠区域,这些区域在生化和结构上均表现出不同。由于堆叠过程会阻塞贴膜的表面,因此无法在膜堆叠区域中对光合膜外表面进行结构或生化研究。尽管在该表面介导了堆叠,但是尚不可能确定在堆叠过程中涉及的膜成分(包括主要的光收集复合物(LHC-II))是否实际上暴露在膜表面。我们已经能够曝光该表面以便在电子显微镜下研究,并直接用抗体标记它以确定蛋白质的暴露。新暴露的外部堆叠表面的出现突出了光合膜的极端横向异质性。与覆盖有不同粒子的相邻非堆叠表面相比,该表面是光滑的。尽管一些研究人员建议在堆叠膜和非堆叠膜之间存在富含细胞色素b6 / f的边界区域,但我们的结果并未为该概念提供任何结构性支持。为了探索被膜表面的生化特性,我们对LHC-II的氨基末端区域使用了单克隆抗体。该mAb清楚地标记了新暴露的外堆叠表面,但未标记内表面或外非堆叠表面。这些实验结果证实了该复合物的氨基末端区域在膜的外表面在堆叠区域中的存在,并且还表明该复合物在非堆叠膜中基本上不存在。

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