Gao Liang
Department of Chemistry, Stony Brook University, Stony Brook, NY, 11794, USA ; Department of Biochemistry & Cell Biology, Stony Brook University, Stony Brook, NY, 11794, USA.
Biomed Opt Express. 2015 Feb 20;6(3):881-90. doi: 10.1364/BOE.6.000881. eCollection 2015 Mar 1.
Selective plane illumination microscopy (SPIM) allows rapid 3D live fluorescence imaging on biological specimens with high 3D spatial resolution, good optical sectioning capability and minimal photobleaching and phototoxic effect. SPIM gains its advantage by confining the excitation light near the detection focal plane, and its performance is determined by the ability to create a thin, large and uniform excitation light sheet. Several methods have been developed to create such an excitation light sheet for SPIM. However, each method has its own strengths and weaknesses, and tradeoffs must be made among different aspects in SPIM imaging. In this work, we present a strategy to select the excitation light sheet among the latest SPIM techniques, and to optimize its geometry based on spatial resolution, field of view, optical sectioning capability, and the sample to be imaged. Besides the light sheets discussed in this work, the proposed strategy is also applicable to estimate the SPIM performance using other excitation light sheets.
选择性平面照明显微镜(SPIM)能够以高3D空间分辨率、良好的光学切片能力以及最小的光漂白和光毒性效应,对生物样本进行快速3D实时荧光成像。SPIM通过将激发光限制在检测焦平面附近而获得其优势,其性能取决于创建一个薄的、大的且均匀的激发光片的能力。已经开发了几种方法来为SPIM创建这样的激发光片。然而,每种方法都有其自身的优缺点,并且在SPIM成像的不同方面之间必须进行权衡。在这项工作中,我们提出了一种策略,用于在最新的SPIM技术中选择激发光片,并基于空间分辨率、视野、光学切片能力以及待成像的样本优化其几何形状。除了本工作中讨论的光片之外,所提出的策略也适用于使用其他激发光片来估计SPIM性能。