Chmielewski Aleksander K, Kyrsting Anders, Mahou Pierre, Wayland Matthew T, Muresan Leila, Evers Jan Felix, Kaminski Clemens F
Department of Chemical Engineering and Biotechnology, University of Cambridge, Pembroke Street, Cambridge, CB2 3RA, UK.
Department of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge, CB2 3DY, UK.
Sci Rep. 2015 Apr 20;5:9385. doi: 10.1038/srep09385.
Light-sheet microscopy is an increasingly popular technique in the life sciences due to its fast 3D imaging capability of fluorescent samples with low photo toxicity compared to confocal methods. In this work we present a new, fast, flexible and simple to implement method to optimize the illumination light-sheet to the requirement at hand. A telescope composed of two electrically tuneable lenses enables us to define thickness and position of the light-sheet independently but accurately within milliseconds, and therefore optimize image quality of the features of interest interactively. We demonstrated the practical benefit of this technique by 1) assembling large field of views from tiled single exposure each with individually optimized illumination settings; 2) sculpting the light-sheet to trace complex sample shapes within single exposures. This technique proved compatible with confocal line scanning detection, further improving image contrast and resolution. Finally, we determined the effect of light-sheet optimization in the context of scattering tissue, devising procedures for balancing image quality, field of view and acquisition speed.
与共聚焦方法相比,光片显微镜因其对荧光样本具有快速三维成像能力且光毒性低,在生命科学领域越来越受欢迎。在这项工作中,我们提出了一种新的、快速、灵活且易于实施的方法,可根据手头的需求优化照明光片。由两个电可调透镜组成的望远镜使我们能够在毫秒内独立且精确地定义光片的厚度和位置,从而交互式地优化感兴趣特征的图像质量。我们通过以下方式证明了该技术的实际优势:1)从拼接的单次曝光中组装大视野,每次曝光都有单独优化的照明设置;2)在单次曝光中塑造光片以追踪复杂的样本形状。该技术被证明与共聚焦线扫描检测兼容,进一步提高了图像对比度和分辨率。最后,我们确定了光片优化在散射组织背景下的效果,设计了平衡图像质量、视野和采集速度的程序。