Department of Chemistry, Columbia University, New York, NY, USA.
Department of Applied Physics and Applied Mathematics, Columbia University, New York, NY, USA.
Nat Commun. 2021 Feb 26;12(1):1305. doi: 10.1038/s41467-021-21570-0.
Imaging the spatial distribution of biomolecules is at the core of modern biology. The development of fluorescence techniques has enabled researchers to investigate subcellular structures with nanometer precision. However, multiplexed imaging, i.e. observing complex biological networks and interactions, is mainly limited by the fundamental 'spectral crowding' of fluorescent materials. Raman spectroscopy-based methods, on the other hand, have a much greater spectral resolution, but often lack the required sensitivity for practical imaging of biomarkers. Addressing the pressing need for new Raman probes, herein we present a series of Raman-active nanoparticles (Rdots) that exhibit the combined advantages of ultra-brightness and compact sizes (~20 nm). When coupled with the emerging stimulated Raman scattering (SRS) microscopy, these Rdots are brighter than previously reported Raman-active organic probes by two to three orders of magnitude. We further obtain evidence supporting for SRS imaging of Rdots at single particle level. The compact size and ultra-brightness of Rdots allows immunostaining of specific protein targets (including cytoskeleton and low-abundant surface proteins) in mammalian cells and tissue slices with high imaging contrast. These Rdots thus offer a promising tool for a large range of studies on complex biological networks.
生物分子的空间分布成像处于现代生物学的核心。荧光技术的发展使研究人员能够以纳米级精度研究亚细胞结构。然而,多重成像,即观察复杂的生物网络和相互作用,主要受到荧光材料基本的“光谱拥挤”限制。基于拉曼光谱的方法具有更大的光谱分辨率,但通常缺乏对生物标志物实际成像所需的灵敏度。为了解决对新型拉曼探针的迫切需求,我们在此展示了一系列具有超亮和紧凑尺寸(~20nm)的拉曼活性纳米颗粒(Rdots)。当与新兴的受激拉曼散射(SRS)显微镜结合使用时,这些 Rdots 的亮度比以前报道的拉曼活性有机探针高两到三个数量级。我们进一步获得了支持 Rdots 在单颗粒水平上进行 SRS 成像的证据。Rdots 的紧凑尺寸和超亮度允许对哺乳动物细胞和组织切片中的特定蛋白质靶标(包括细胞骨架和低丰度表面蛋白)进行免疫染色,具有高成像对比度。因此,这些 Rdots 为研究复杂生物网络提供了一种很有前途的工具。