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用于细胞和组织纳米级分子分析的扩展与波动增强显微镜技术。

Expansion and fluctuations-enhanced microscopy for nanoscale molecular profiling of cells and tissues.

作者信息

Kylies Dominik, Heil Hannah S, Vesga Arturo G, Del Rosario Mario, Schwerk Maria, Kuehl Malte, Wong Milagros N, Puelles Victor G, Henriques Ricardo

机构信息

III. Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Hamburg Center for Kidney Health (HCKH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Nat Protoc. 2025 Jul 2. doi: 10.1038/s41596-025-01178-0.

Abstract

Advances in super-resolution microscopy enable the molecular profiling of cells and tissues at the nanoscale level, surpassing the diffraction limit of conventional light microscopy. However, super-resolution techniques typically require access to expensive specialized equipment and extensive training, limiting their broad applicability. Here we provide a detailed protocol for combining expansion microscopy with enhanced super-resolution radial fluctuations analysis to achieve nanoscale resolution using conventional microscopes. Expansion microscopy physically enlarges the sample, while enhanced super-resolution radial fluctuations computationally enhances the image resolution by analyzing fluorescence fluctuations over time. By combining both, we achieve images with a resolution of 25 nm in combination with diffraction-limited microscopes. Our step-by-step instructions include the expansion of cells and tissue samples, the optimization of multispectral microscopy parameters and the implementation of quality control metrics to minimize artifacts. We further cover the use of quantitative tools such as NanoJ-SQUIRREL, which enable the assessment of resolution improvements and image fidelity. We discuss key considerations for each stage, including sample preparation, image acquisition, computational processing and downstream analysis. Potential pitfalls and troubleshooting strategies are also addressed. This protocol can be used for imaging a variety of sample types with multiple fluorescent labels. With nanoscale spatial resolution and molecular specificity, expansion-enhanced super-resolution radial fluctuations microscopy provides a flexible, accessible approach for investigating cellular ultrastructure, protein localization and interaction networks, suitable for applications in cell biology, histopathology and biomedical research. The procedure requires 3-4 d to complete, involving ~7-9 h of total bench, imaging and processing time and only requires basic expertise in tissue handling, molecular and cell biology, and microscopy.

摘要

超分辨率显微镜技术的进步使得在纳米尺度上对细胞和组织进行分子剖析成为可能,突破了传统光学显微镜的衍射极限。然而,超分辨率技术通常需要使用昂贵的专用设备并经过大量培训,这限制了它们的广泛应用。在此,我们提供了一份详细的方案,将扩张显微镜与增强型超分辨率径向涨落分析相结合,以便使用传统显微镜实现纳米级分辨率。扩张显微镜通过物理方法放大样本,而增强型超分辨率径向涨落分析则通过分析荧光随时间的涨落来在计算上提高图像分辨率。通过将两者结合,我们使用衍射极限显微镜获得了分辨率为25纳米的图像。我们的分步说明包括细胞和组织样本的扩张、多光谱显微镜参数的优化以及质量控制指标的实施,以尽量减少伪像。我们还介绍了诸如NanoJ-SQUIRREL等定量工具的使用,这些工具能够评估分辨率的提高和图像保真度。我们讨论了每个阶段的关键注意事项,包括样本制备、图像采集、计算处理和下游分析。还讨论了潜在的陷阱和故障排除策略。该方案可用于对具有多种荧光标记的各种样本类型进行成像。凭借纳米级空间分辨率和分子特异性,扩张增强型超分辨率径向涨落显微镜为研究细胞超微结构、蛋白质定位和相互作用网络提供了一种灵活、易用的方法,适用于细胞生物学、组织病理学和生物医学研究。该过程需要3至4天完成,总共需要约7至9小时的实验台操作、成像和处理时间,并且仅需要在组织处理、分子和细胞生物学以及显微镜方面具备基本专业知识。

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