Laboratoire de Physique des Solides, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 8502, Université Paris-Sud XI, 91405 Orsay cedex, France.
Proc Natl Acad Sci U S A. 2012 Jun 5;109(23):8959-64. doi: 10.1073/pnas.1200881109. Epub 2012 May 21.
Using cryoelectron microscopy of vitreous sections, we investigated in situ the ultrastructure of biological membranes, selected from several cell types for their diverse biological functions. Here we describe how to visualize the two membrane leaflets and tightly apposed membranes, lying as close as 1.1 nm apart, by tuning the imaging conditions. We show how defects in membrane stacks may be clues to resolving their structure. Details of membrane proteins are also resolved, as well as protein lattices with correlations between stacked membranes. Imaging the cell in its native hydrated state can now be done in the nanometer resolution range, which should open unique routes for investigating structure-function relationships.
利用玻璃切片的冷冻电子显微镜,我们针对不同的生物功能,从几种细胞类型中选择了生物膜进行原位超微结构研究。本文描述了如何通过调整成像条件来可视化两个膜小叶和紧密贴合的膜,它们之间的距离只有 1.1nm。我们展示了如何通过膜堆叠中的缺陷来揭示其结构。还可以分辨膜蛋白的细节以及堆叠膜之间具有相关性的蛋白质晶格。现在可以在纳米分辨率范围内对细胞进行其天然水合状态成像,这应该为研究结构-功能关系开辟独特的途径。