Department of Bioengineering, University of Texas at Arlington, Arlington, TX 75022, USA.
Int J Mol Sci. 2022 Jan 31;23(3):1643. doi: 10.3390/ijms23031643.
Optical microscopy has vastly expanded the frontiers of structural and functional biology, due to the non-invasive probing of dynamic volumes in vivo. However, traditional widefield microscopy illuminating the entire field of view (FOV) is adversely affected by out-of-focus light scatter. Consequently, standard upright or inverted microscopes are inept in sampling diffraction-limited volumes smaller than the optical system's point spread function (PSF). Over the last few decades, several planar and structured (sinusoidal) illumination modalities have offered unprecedented access to sub-cellular organelles and 4D (3D + time) image acquisition. Furthermore, these optical sectioning systems remain unaffected by the size of biological samples, providing high signal-to-noise (SNR) ratios for objective lenses (OLs) with long working distances (WDs). This review aims to guide biologists regarding planar illumination strategies, capable of harnessing sub-micron spatial resolution with a millimeter depth of penetration.
光学显微镜通过对体内动态容积进行非侵入性探测,极大地拓展了结构和功能生物学的前沿领域。然而,传统的全场照明宽场显微镜会受到离焦光散射的不利影响。因此,标准的正置或倒置显微镜在采集小于光学系统点扩散函数 (PSF) 的衍射极限体积方面能力不足。在过去的几十年中,几种平面和结构(正弦)照明模式为亚细胞细胞器和 4D(3D+时间)图像采集提供了前所未有的获取途径。此外,这些光学切片系统不受生物样品大小的影响,为具有长工作距离 (WD) 的物镜 (OL) 提供了高信噪比 (SNR) 比值。本综述旨在为生物学家提供指导,了解能够利用亚微米空间分辨率实现毫米穿透深度的平面照明策略。