de Medeiros Gustavo, Norlin Nils, Gunther Stefan, Albert Marvin, Panavaite Laura, Fiuza Ulla-Maj, Peri Francesca, Hiiragi Takashi, Krzic Uros, Hufnagel Lars
European Molecular Biology Laboratory, Cell Biology and Biophysics Unit, Meyerhofstrasse 1, 69117, Heidelberg, Germany.
European Molecular Biology Laboratory, Developmental Biology Unit, Meyerhofstrasse 1, 69117, Heidelberg, Germany.
Nat Commun. 2015 Nov 25;6:8881. doi: 10.1038/ncomms9881.
Selective-plane illumination microscopy has proven to be a powerful imaging technique due to its unsurpassed acquisition speed and gentle optical sectioning. However, even in the case of multiview imaging techniques that illuminate and image the sample from multiple directions, light scattering inside tissues often severely impairs image contrast. Here we combine multiview light-sheet imaging with electronic confocal slit detection implemented on modern camera sensors. In addition to improved imaging quality, the electronic confocal slit detection doubles the acquisition speed in multiview setups with two opposing illumination directions allowing simultaneous dual-sided illumination. Confocal multiview light-sheet microscopy eliminates the need for specimen-specific data fusion algorithms, streamlines image post-processing, easing data handling and storage.
选择性平面照明显微镜已被证明是一种强大的成像技术,因其具有无与伦比的采集速度和温和的光学切片功能。然而,即使在从多个方向照射和成像样本的多视图成像技术中,组织内部的光散射也常常严重损害图像对比度。在这里,我们将多视图光片成像与现代相机传感器上实现的电子共焦狭缝检测相结合。除了提高成像质量外,电子共焦狭缝检测还使具有两个相反照明方向的多视图设置中的采集速度提高了一倍,从而实现同时双面照明。共焦多视图光片显微镜无需特定于样本的数据融合算法,简化了图像后处理,便于数据处理和存储。