Duinkerken B H Peter, Alsahaf Ahmad M J, Hoogenboom Jacob P, Giepmans Ben N G
Department of Biomedical Sciences, University Groningen, University Medical Centre Groningen, Groningen, AV, The Netherlands.
Department of Imaging Physics, Delft University of Technology, Delft, CJ, The Netherlands.
Npj Imaging. 2024 Dec 11;2(1):53. doi: 10.1038/s44303-024-00059-7.
Microscopy is a key technique to visualize and understand biology. Electron microscopy (EM) facilitates the investigation of cellular ultrastructure at biomolecular resolution. Cellular EM was recently revolutionized by automation and digitalisation allowing routine capture of large areas and volumes at nanoscale resolution. Analysis, however, is hampered by the greyscale nature of electron images and their large data volume, often requiring laborious manual annotation. Here we demonstrate unsupervised and automated extraction of biomolecular assemblies in conventionally processed tissues using large-scale hyperspectral energy-dispersive X-ray (EDX) imaging. First, we discriminated biological features in the context of tissue based on selected elemental maps. Next, we designed a data-driven workflow based on dimensionality reduction and spectral mixture analysis, allowing the visualization and isolation of subcellular features with minimal manual intervention. Broad implementations of the presented methodology will accelerate the understanding of biological ultrastructure.
显微镜检查是可视化和理解生物学的关键技术。电子显微镜(EM)有助于在生物分子分辨率下研究细胞超微结构。细胞电子显微镜最近因自动化和数字化而发生了变革,能够以纳米级分辨率常规捕获大面积和大体积的图像。然而,分析受到电子图像的灰度性质及其大数据量的阻碍,通常需要费力的手动注释。在这里,我们展示了使用大规模高光谱能量色散X射线(EDX)成像在传统处理的组织中无监督自动提取生物分子组装体的方法。首先,我们基于选定的元素图谱在组织背景下区分生物学特征。接下来,我们设计了一种基于降维和光谱混合分析的数据驱动工作流程,能够以最少的人工干预实现亚细胞特征的可视化和分离。所提出方法的广泛应用将加速对生物超微结构的理解。