Conchello José-Angel, Lichtman Jeff W
Molecular, Cell, and Developmental Biology, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma 73104, USA.
Nat Methods. 2005 Dec;2(12):920-31. doi: 10.1038/nmeth815.
Confocal scanning microscopy, a form of optical sectioning microscopy, has radically transformed optical imaging in biology. These devices provide a powerful means to eliminate from images the background caused by out-of-focus light and scatter. Confocal techniques can also improve the resolution of a light microscope image beyond what is achievable with widefield fluorescence microscopy. The quality of the images obtained, however, depends on the user's familiarity with the optical and fluorescence concepts that underlie this approach. We describe the core concepts of confocal microscopes and important variables that adversely affect confocal images. We also discuss data-processing methods for confocal microscopy and computational optical sectioning techniques that can perform optical sectioning without a confocal microscope.
共聚焦扫描显微镜是光学切片显微镜的一种形式,它彻底改变了生物学中的光学成像。这些设备提供了一种强大的方法,可从图像中消除由离焦光和散射引起的背景。共聚焦技术还可以提高光学显微镜图像的分辨率,超越宽场荧光显微镜所能达到的水平。然而,所获得图像的质量取决于用户对这种方法所基于的光学和荧光概念的熟悉程度。我们描述了共聚焦显微镜的核心概念以及对共聚焦图像有不利影响的重要变量。我们还讨论了共聚焦显微镜的数据处理方法以及无需共聚焦显微镜即可执行光学切片的计算光学切片技术。