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1
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Nanophotonics. 2019 Dec;8(12):2111-2128. doi: 10.1515/nanoph-2019-0227. Epub 2019 Sep 28.
2
Optical volumetric projection with large NA objectives for fast high-resolution 3D imaging of neural signals.用于神经信号快速高分辨率三维成像的大数值孔径物镜光学体积投影。
Biomed Opt Express. 2020 Jun 16;11(7):3769-3782. doi: 10.1364/BOE.393494. eCollection 2020 Jul 1.
3
Fast and accurate sCMOS noise correction for fluorescence microscopy.快速准确的 sCMOS 荧光显微镜噪声校正。
Nat Commun. 2020 Jan 3;11(1):94. doi: 10.1038/s41467-019-13841-8.
4
Gene expression amplification by nuclear speckle association.核斑关联导致基因表达扩增。
J Cell Biol. 2020 Jan 6;219(1). doi: 10.1083/jcb.201904046.
5
Strategies for increasing the throughput of super-resolution microscopies.提高超分辨率显微镜通量的策略。
Curr Opin Chem Biol. 2019 Aug;51:84-91. doi: 10.1016/j.cbpa.2019.05.012. Epub 2019 Jun 15.
6
SABER amplifies FISH: enhanced multiplexed imaging of RNA and DNA in cells and tissues.SABER 增强 FISH:在细胞和组织中增强 RNA 和 DNA 的多重成像。
Nat Methods. 2019 Jun;16(6):533-544. doi: 10.1038/s41592-019-0404-0. Epub 2019 May 20.
7
Transcriptome-scale super-resolved imaging in tissues by RNA seqFISH.基于 RNA seqFISH 的转录组尺度超分辨组织成像
Nature. 2019 Apr;568(7751):235-239. doi: 10.1038/s41586-019-1049-y. Epub 2019 Mar 25.
8
Nuclear speckle fusion via long-range directional motion regulates speckle morphology after transcriptional inhibition.核斑点融合通过长程定向运动调节转录抑制后的斑点形态。
J Cell Sci. 2019 Apr 17;132(8):jcs226563. doi: 10.1242/jcs.226563.
9
Spatial proteomics: a powerful discovery tool for cell biology.空间蛋白质组学:细胞生物学的强大发现工具。
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Content-aware image restoration: pushing the limits of fluorescence microscopy.内容感知图像恢复:推动荧光显微镜的极限。
Nat Methods. 2018 Dec;15(12):1090-1097. doi: 10.1038/s41592-018-0216-7. Epub 2018 Nov 26.

2.5D显微镜技术:通过体积投影实现快速、高通量成像以进行定量亚细胞分析。

2.5D microscopy: Fast, high-throughput imaging via volumetric projection for quantitative subcellular analysis.

作者信息

Ren Jinhan, Han Kyu Young

机构信息

CREOL, The College of Optics and Photonics, University of Central Florida, Orlando, Florida 32816, United States.

出版信息

ACS Photonics. 2021 Mar 17;8(3):933-942. doi: 10.1021/acsphotonics.1c00012. Epub 2021 Feb 25.

DOI:10.1021/acsphotonics.1c00012
PMID:34485614
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8412410/
Abstract

Imaging-based single-cell analysis is essential to study the expression level and functions of biomolecules at subcellular resolution. However, its low throughput has prevented the measurement of numerous cellular features from multiples cells in a rapid and efficient manner. Here we report 2.5D microscopy that significantly improves the throughput of fluorescence imaging systems while maintaining high-resolution and single-molecule sensitivity. Instead of sequential z-scanning, volumetric information is projected onto a 2D image plane in a single shot by engineering the emitted fluorescence light. Our approach provides an improved imaging speed and uniform focal response within a specific imaging depth, which enabled us to perform quantitative single-molecule RNA measurements over a 2×2 mm region within an imaging depth of ~5 μm for mammalian cells in <10 min and immunofluorescence imaging at a >30 Hz volumetric frame rate with reduced photobleaching. Our microscope also offers the ability of multi-color imaging, depth control and super-resolution imaging.

摘要

基于成像的单细胞分析对于在亚细胞分辨率下研究生物分子的表达水平和功能至关重要。然而,其低通量阻碍了以快速有效的方式对多个细胞的众多细胞特征进行测量。在此,我们报告了一种2.5D显微镜技术,该技术在保持高分辨率和单分子灵敏度的同时,显著提高了荧光成像系统的通量。通过对发射的荧光进行处理,体积信息不是通过顺序z扫描,而是在单次拍摄中投影到二维图像平面上。我们的方法在特定成像深度内提供了更高的成像速度和均匀的焦平面响应,这使我们能够在不到10分钟的时间内对哺乳动物细胞在约5μm的成像深度内的2×2mm区域进行定量单分子RNA测量,并以大于30Hz的体积帧率进行免疫荧光成像,同时减少光漂白。我们的显微镜还具备多色成像、深度控制和超分辨率成像的能力。