Shin Younghoon, Kim Dongmok, Kwon Hyuk-Sang
Department of Biomedical Science and Engineering, Institute of Integrated Technology (IIT), Gwangju Institute of Science and Technology (GIST), Gwangju, South Korea.
J Biophotonics. 2018 May;11(5):e201700270. doi: 10.1002/jbio.201700270. Epub 2018 Feb 2.
Light-sheet fluorescence microscopy (LSFM) is a powerful tool for biological studies because it allows for optical sectioning of dynamic samples with superior temporal resolution. However, LSFM using 2 orthogonally co-aligned objectives requires a special sample geometry, and volumetric imaging speed is limited due to physical sample translation. This paper describes an oblique scanning 2-photon LSFM (OS-2P-LSFM) that eliminates these limitations by using a single objective near the sample and a refractive scanning-descanning system. This system also provides improved light-sheet confinement against scattering by using a 2-photon Bessel beam. The OS-2P-LSFM hold promise for studying structural, functional and dynamic aspects of living tissues and organisms because it allows for high-speed, translation-free and scattering-robust 3D imaging of large biological specimens.
光片荧光显微镜(LSFM)是生物学研究的强大工具,因为它能够以卓越的时间分辨率对动态样本进行光学切片。然而,使用两个正交共对准物镜的LSFM需要特殊的样本几何形状,并且由于物理样本平移,体积成像速度受到限制。本文描述了一种斜扫描双光子LSFM(OS-2P-LSFM),它通过在样本附近使用单个物镜和折射扫描-解扫描系统消除了这些限制。该系统还通过使用双光子贝塞尔光束改善了光片对散射的限制。OS-2P-LSFM有望用于研究活组织和生物体的结构、功能和动态方面,因为它能够对大型生物样本进行高速、无平移和抗散射的三维成像。