Department of Life Sciences and the National Institute for Biotechnology in the Negev, Ben-Gurion University, 84105 Beer-Sheva, Israel.
Department of Biochemistry, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland.
Structure. 2018 Oct 2;26(10):1408-1413.e3. doi: 10.1016/j.str.2018.06.009. Epub 2018 Aug 2.
Gold nanoparticles (AuNPs) and their conjugation to biological samples have numerous potential applications. When combined with cryo-electron microscopy and tomography analysis, AuNPs may provide a versatile and powerful tool to identify and precisely localize proteins even when attached to cellular components. Here, we describe a general and facile approach for the synthesis of homogeneous and stable AuNPs, which can readily be conjugated to a molecule of interest and imaged by cryo-electron tomography (cryo-ET). We demonstrate the synthesis of 2.2 ± 0.45-nm tiopronin-protected AuNPs, followed by their conjugation with recombinant proteins and peptides. Visualization of the ∼2.2-nm gold-tagged peptides by cryo-ET reveals the potential use of this strategy to label and localize accessible proteins in a cellular environment with nanometric resolution.
金纳米粒子(AuNPs)及其与生物样本的结合具有许多潜在的应用。当与低温电子显微镜和断层分析结合使用时,AuNPs 可能提供一种通用且强大的工具,即使在与细胞成分结合的情况下,也可以识别和精确定位蛋白质。在这里,我们描述了一种通用且简便的方法来合成均匀且稳定的 AuNPs,这些 AuNPs 可以很容易地与感兴趣的分子结合,并通过低温电子断层扫描(cryo-ET)进行成像。我们展示了 2.2±0.45nm 巯基丙氨酸保护的 AuNPs 的合成,随后将其与重组蛋白和肽结合。通过低温电子断层扫描对约 2.2nm 的金标记肽进行可视化,揭示了该策略在纳米级分辨率下标记和定位细胞环境中可及蛋白质的潜在用途。