Brock R, Jovin T M
Department of Molecular Biology, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany.
Cell Mol Biol (Noisy-le-grand). 1998 Jul;44(5):847-56.
Confocal fluorescence correlation spectroscopy (FCS) and other confocal spectroscopic techniques are ideally suited for the analysis of molecular interactions at the subcellular level. However, one requires exact positioning in three dimensions within the cell. Our instrument integrates FCS with high sensitivity digital imaging microscopy and high precision positioning. We present first measurements of intracellular FCS, with specification of the instrumental requirements and methods of data analysis. We propose the term fluorescence correlation microscopy (FCM) for this extended modality of FCS.
共焦荧光相关光谱法(FCS)及其他共焦光谱技术非常适合用于分析亚细胞水平的分子相互作用。然而,需要在细胞内进行精确的三维定位。我们的仪器将FCS与高灵敏度数字成像显微镜及高精度定位相结合。我们展示了细胞内FCS的首次测量结果,并说明了仪器要求和数据分析方法。我们提议将这种FCS的扩展模式称为荧光相关显微镜(FCM)。