通过棱镜照明和微流体增强 DNA-PAINT 对细胞和组织切片进行多路复用和毫米级荧光纳米观察

Matthew J. Rames, John P. Kenison, Daniel Heineck, Fehmi Civitci, Malwina Szczepaniak, Ting Zheng, Julia Shangguan, Yujia Zhang, Kai Tao, Sadik Esener and Xiaolin Nan*, 
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引用次数: 0

摘要

荧光纳米镜在生物医学研究中的作用越来越强大,但它的视场(FOV)一直很小,一次大约为 50 μm × 50 μm,最近甚至达到了 ∼200 μm × 200 μm。迄今为止,要进一步提高荧光纳米透视的视场角,主要依赖于使用制造的波导基底,这增加了应用的成本和样品限制。在此,我们报告了 PRism-Illumination and Microfluidics-Enhanced DNA-PAINT (PRIME-PAINT),用于毫米级 FOV 的多路复用荧光纳米镜。PRIME-PAINT 建立在成熟的棱镜式全内反射显微镜基础之上,可实现强大的单分子定位,单个视场可达 520 μm × 520 μm,横向分辨率为 25-40 nm。通过拼接,每个目标可在短短 40 分钟内完成平方毫米样品区域的纳米成像。阶段式微流控室便于多路复用的探针交换,并提高图像质量,尤其是福尔马林固定石蜡包埋(FFPE)组织切片的图像质量。我们分析了 1000 个细胞中的 106 个洞穴结构,并对患者组织切片中的整个胰腺癌病灶进行了成像,从而证明了 PRIME-PAINT 的实用性。通过从纳米到毫米的多重成像和广泛的样本兼容性,PRIME-PAINT 将有助于建立多尺度、类似谷歌地球的生物系统视图。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Multiplexed and Millimeter-Scale Fluorescence Nanoscopy of Cells and Tissue Sections via Prism-Illumination and Microfluidics-Enhanced DNA-PAINT

Multiplexed and Millimeter-Scale Fluorescence Nanoscopy of Cells and Tissue Sections via Prism-Illumination and Microfluidics-Enhanced DNA-PAINT

Fluorescence nanoscopy has become increasingly powerful for biomedical research, but it has historically afforded a small field-of-view (FOV) of around 50 μm × 50 μm at once and more recently up to ∼200 μm × 200 μm. Efforts to further increase the FOV in fluorescence nanoscopy have thus far relied on the use of fabricated waveguide substrates, adding cost and sample constraints to the applications. Here we report PRism-Illumination and Microfluidics-Enhanced DNA-PAINT (PRIME-PAINT) for multiplexed fluorescence nanoscopy across millimeter-scale FOVs. Built upon the well-established prism-type total internal reflection microscopy, PRIME-PAINT achieves robust single-molecule localization with up to ∼520 μm × 520 μm single FOVs and 25–40 nm lateral resolutions. Through stitching, nanoscopic imaging over mm2 sample areas can be completed in as little as 40 min per target. An on-stage microfluidics chamber facilitates probe exchange for multiplexing and enhances image quality, particularly for formalin-fixed paraffin-embedded (FFPE) tissue sections. We demonstrate the utility of PRIME-PAINT by analyzing ∼106 caveolae structures in ∼1,000 cells and imaging entire pancreatic cancer lesions from patient tissue biopsies. By imaging from nanometers to millimeters with multiplexity and broad sample compatibility, PRIME-PAINT will be useful for building multiscale, Google-Earth-like views of biological systems.

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来源期刊
Chemical & Biomedical Imaging
Chemical & Biomedical Imaging 化学与生物成像-
CiteScore
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期刊介绍: Chemical & Biomedical Imaging is a peer-reviewed open access journal devoted to the publication of cutting-edge research papers on all aspects of chemical and biomedical imaging. This interdisciplinary field sits at the intersection of chemistry physics biology materials engineering and medicine. The journal aims to bring together researchers from across these disciplines to address cutting-edge challenges of fundamental research and applications.Topics of particular interest include but are not limited to:Imaging of processes and reactionsImaging of nanoscale microscale and mesoscale materialsImaging of biological interactions and interfacesSingle-molecule and cellular imagingWhole-organ and whole-body imagingMolecular imaging probes and contrast agentsBioluminescence chemiluminescence and electrochemiluminescence imagingNanophotonics and imagingChemical tools for new imaging modalitiesChemical and imaging techniques in diagnosis and therapyImaging-guided drug deliveryAI and machine learning assisted imaging
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