Feofanov A V, Grishin A I, Kudelina I A, Shitova L A, Karmakova T A, Iakubovskaia R I, Egret-Charlier M, Vigny P
Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, Russia.
Bioorg Khim. 1999 Dec;25(12):892-902.
The confocal spectral imaging (CSI) technique is described, its basic principles are considered, and a brief review of its applications to the study of biologically active compounds (BAC) within living cells and in tissue slices is presented. This technique is based on measurements and analysis of fluorescence or resonance Raman spectra in each point of the specimen under microscope with a three-dimensional resolution of about cubic micrometer. This technique is applicable to the study of stained fluorescent and nonfluorescent compounds. Unlike the conventional approaches based on the optical microscopy, the CSI technique opens the opportunity for the identification of complexes and microenvironment of BAC in intact cells and thin tissue slices (slices or sections), as well as for the analysis of localization and distribution of compounds of interest and their complexes in cellular organelles and tissue structures. The use of CSI technique in combination with the conventional biochemical and cytological methods makes it possible to significantly expand the informativeness of investigation of modes of action of new BAC.
介绍了共焦光谱成像(CSI)技术,探讨了其基本原理,并简要回顾了该技术在活细胞和组织切片中生物活性化合物(BAC)研究中的应用。该技术基于在显微镜下对标本各点的荧光或共振拉曼光谱进行测量和分析,三维分辨率约为立方微米。该技术适用于对染色的荧光和非荧光化合物的研究。与基于光学显微镜的传统方法不同,CSI技术为鉴定完整细胞和薄组织切片(切片或断面)中BAC的复合物和微环境提供了机会,也为分析感兴趣的化合物及其复合物在细胞器和组织结构中的定位和分布提供了可能。将CSI技术与传统的生化和细胞学方法结合使用,可以显著扩展对新型BAC作用模式研究的信息量。