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传播路径均匀扫描光片激发显微镜,用于大样本各向同性体积成像。

Propagating-path uniformly scanned light sheet excitation microscopy for isotropic volumetric imaging of large specimens.

机构信息

Huazhong Univ. of Science and Technology, China.

Britton Chance Ctr. for Biomedical Photonics, China.

出版信息

J Biomed Opt. 2019 Aug;24(8):1-5. doi: 10.1117/1.JBO.24.8.086501.

Abstract

We demonstrate a propagating-path uniformly scanned light sheet excitation (PULSE) microscopy based on the oscillation of voice coil motor that can rapidly drive a thin light sheet along its propagation direction. By synchronizing the rolling shutter of a camera with the motion of laser sheet, we can obtain a uniform plane-illuminated image far beyond the confocal range of Gaussian beam. A stable 1.7-μm optical sectioning under a 3.3  mm  ×  3.3  mm wide field of view (FOV) has been achieved for up to 20 Hz volumetric imaging of large biological specimens. PULSE method transforms the extent of plane illumination from one intrinsically limited by the short confocal range (μm scale) to one defined by the motor oscillation range (mm scale). Compared to the conventional Gaussian light sheet imaging, our method greatly mitigates the compromise of axial resolution and successfully extends the FOV over 100 times. We demonstrate the applications of PULSE method by rapidly imaging cleared mouse spinal cord and live zebrafish larva at isotropic subcellular resolution.

摘要

我们展示了一种基于音圈电机振荡的传播路径均匀扫描光片激发(PULSE)显微镜,它可以沿传播方向快速驱动薄光片。通过使相机的卷帘快门与激光片的运动同步,我们可以获得远远超出高斯光束共焦范围的均匀平面照明图像。在 3.3mm×3.3mm 的大视场下,实现了稳定的 1.7μm 光学切片,最大可达 20Hz 的大生物样本体积成像。PULSE 方法将平面照明的范围从固有地受到短共焦范围(μm 级)限制的程度,转变为受到电机振荡范围(mm 级)限制的程度。与传统的高斯光片成像相比,我们的方法大大减轻了轴向分辨率的折衷,并成功地将视场扩展了 100 多倍。我们通过快速成像透明化的小鼠脊髓和活体斑马鱼幼虫,以各向同性的亚细胞分辨率展示了 PULSE 方法的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f69e/6983483/3148e861cbb5/JBO-024-086501-g001.jpg

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