Lake Michael P, Bouchard Louis-S
Department of Chemistry and Biochemistry, University of California, Los Angeles, California, United States of America.
California NanoSystems Institute, University of California, Los Angeles, California, United States of America.
PLoS One. 2017 Jun 21;12(6):e0179295. doi: 10.1371/journal.pone.0179295. eCollection 2017.
Transmission electron microscopy (TEM) can be used to successfully determine the structures of proteins. However, such studies are typically done ex situ after extraction of the protein from the cellular environment. Here we describe an application for nanodiamonds as targeted intensity contrast labels in biological TEM, using the nuclear pore complex (NPC) as a model macroassembly. We demonstrate that delivery of antibody-conjugated nanodiamonds to live mammalian cells using maltotriose-conjugated polypropylenimine dendrimers results in efficient localization of nanodiamonds to the intended cellular target. We further identify signatures of nanodiamonds under TEM that allow for unambiguous identification of individual nanodiamonds from a resin-embedded, OsO4-stained environment. This is the first demonstration of nanodiamonds as labels for nanoscale TEM-based identification of subcellular protein assemblies. These results, combined with the unique fluorescence properties and biocompatibility of nanodiamonds, represent an important step toward the use of nanodiamonds as markers for correlated optical/electron bioimaging.
透射电子显微镜(TEM)可用于成功确定蛋白质的结构。然而,此类研究通常是在从细胞环境中提取蛋白质后在非原位条件下进行的。在此,我们描述了一种将纳米金刚石用作生物TEM中靶向强度对比标记的应用,以核孔复合体(NPC)作为模型大分子组装体。我们证明,使用麦芽三糖共轭的聚丙撑亚胺树枝状大分子将抗体共轭的纳米金刚石递送至活的哺乳动物细胞,可使纳米金刚石有效地定位到预期的细胞靶点。我们进一步在TEM下识别出纳米金刚石的特征,从而能够在树脂包埋、OsO4染色的环境中明确识别单个纳米金刚石。这是首次证明纳米金刚石可作为基于TEM的纳米级亚细胞蛋白质组装体识别的标记。这些结果,再加上纳米金刚石独特的荧光特性和生物相容性,代表了朝着将纳米金刚石用作相关光学/电子生物成像标记迈出的重要一步。