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

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 st...

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Bibliographic Details
Main Authors: Xu, Dongli, Zhou, Weibin, Peng, Leilei
Other Authors: Univ Arizona, Coll Opt Sci
Language:en
Published: OPTICAL SOC AMER 2017
Online Access:http://hdl.handle.net/10150/626463
http://arizona.openrepository.com/arizona/handle/10150/626463
Description
Summary: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 mu m deep with 0.5 mu m-by-2 mu m (lateral-by-axial) resolution. (C) 2017 Optical Society of America under the terms of the OSA Open Access Publishing Agreement