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具有同步激发-多路复用结构照明的三维实时多标记光片成像

Three-dimensional live multi-label light-sheet imaging with synchronous excitation-multiplexed structured illumination.

作者信息

Xu Dongli, Zhou Weibin, Peng Leilei

出版信息

Opt Express. 2017 Dec 11;25(25):31159-31173. doi: 10.1364/OE.25.031159.

Abstract

Multiplexed imaging is a powerful tool for studying complex interactions inside biological systems. Spectral imaging methods that capture multiple fluorescent markers synchronously without sacrificing the imaging speed or resolution are most suitable for live imaging. We describe spectral-encoded structured illumination (spectral-SIM) light-sheet microscopy, which enables parallel multi-excitation-channel imaging in 3D. Spectral-SIM encodes the excitation wavelength as the phase of the illumination pattern, and allows synchronous image capture over multiple excitation channels at the same speed and spatial resolution as mono-channel structured light-sheet imaging. The technique retains structured light-sheet microscopy's ability in removing out-of-focus and scattered emission background, and generates clear 3D multiplexed images in thick tissue. The capability of this technique was demonstrated by the imaging of live triple-labeled transgenic zebrafish to over 300 μm deep with 0.5μm-by-2μm (lateral-by-axial) resolution.

摘要

多重成像技术是研究生物系统内部复杂相互作用的有力工具。能在不牺牲成像速度或分辨率的情况下同步捕获多个荧光标记的光谱成像方法最适合用于实时成像。我们介绍了光谱编码结构照明显微术(spectral-SIM),它能够在三维空间中进行并行多激发通道成像。光谱-SIM将激发波长编码为照明图案的相位,并允许以与单通道结构光片成像相同的速度和空间分辨率在多个激发通道上同步采集图像。该技术保留了结构光片显微镜去除离焦和散射发射背景的能力,并能在厚组织中生成清晰的三维多重图像。通过对活的三标记转基因斑马鱼进行成像,以0.5微米×2微米(横向×轴向)的分辨率深入超过300微米,证明了该技术的能力。

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