He Yongning, Jensen Grant J, Bjorkman Pamela J
Division of Biology, California Institute of Technology, 114-96, 1200 East California Blvd., Pasadena, CA 91125, USA.
Microsc Microanal. 2009 Jun;15(3):183-8. doi: 10.1017/S1431927609090424.
While electron cryotomography (ECT) provides "molecular" resolution, three-dimensional images of unique biological specimens, sample crowdedness, and/or resolution limitations can make it difficult to identify specific macromolecular components. Here we used a 1.4 nm Nanogold cluster specifically attached to the Fc fragment of IgG to monitor its interaction with the neonatal Fc receptor (FcRn), a membrane-bound receptor that transports IgG across cells in acidic intracellular vesicles. ECT was used to image complexes formed by Nanogold-labeled Fc bound to FcRn attached to the outer surface of synthetic liposomes. In the resulting three-dimensional reconstructions, 1.4 nm Nanogold particles were distributed predominantly along the interfaces where 2:1 FcRn-Fc complexes bridged adjacent lipid bilayers. These results demonstrate that the 1.4 nm Nanogold cluster is visible in tomograms of typically thick samples (approximately 250 nm) recorded with defocuses appropriate for large macromolecules and is thus an effective marker.
虽然电子冷冻断层扫描(ECT)能提供独特生物标本的“分子”分辨率三维图像,但样本拥挤和/或分辨率限制可能使其难以识别特定的大分子成分。在这里,我们使用了一种特异性附着于IgG Fc片段的1.4纳米纳米金簇来监测其与新生儿Fc受体(FcRn)的相互作用,FcRn是一种膜结合受体,可在酸性细胞内囊泡中跨细胞转运IgG。ECT用于对纳米金标记的Fc与附着在合成脂质体外表面的FcRn结合形成的复合物进行成像。在所得的三维重建中,1.4纳米的纳米金颗粒主要沿2:1 FcRn-Fc复合物桥接相邻脂质双层的界面分布。这些结果表明,1.4纳米的纳米金簇在用适合大分子的散焦记录的典型厚样本(约250纳米)的断层图像中可见,因此是一种有效的标记物。