Badon Amaury, Bensussen Seth, Gritton Howard J, Awal Mehraj R, Gabel Christopher V, Han Xue, Mertz Jerome
Department of Biomedical Engineering, Boston University, Boston, Massachusetts 02215, USA.
Department of Physiology and Biophysics, Boston University School of Medicine, Boston, Massachusetts 02218, USA.
Optica. 2019 Apr 20;6(4):389-395. doi: 10.1364/optica.6.000389. Epub 2019 Mar 21.
Fast, volumetric imaging over large scales has been a long-standing challenge in biological microscopy. To address this challenge, we report an augmented variant of confocal microscopy that uses a series of reflecting pinholes axially distributed in the detection space, such that each pinhole probes a different depth within the sample. We thus obtain simultaneous multiplane imaging without the need for axial scanning. Our microscope technique is versatile and configured here to provide two-color fluorescence imaging with a field of view larger than a millimeter at video rate. Its general applicability is demonstrated with neuronal imaging of both and mouse brains .
在生物显微镜领域,快速、大尺度的体积成像一直是一项长期存在的挑战。为应对这一挑战,我们报告了一种共聚焦显微镜的增强变体,它使用一系列轴向分布在检测空间中的反射针孔,使得每个针孔探测样品内不同的深度。因此,我们无需轴向扫描就能获得同步多平面成像。我们的显微镜技术用途广泛,在此配置下可在视频速率下提供视野大于一毫米的双色荧光成像。其在果蝇和小鼠大脑的神经元成像中展示了普遍适用性。