Pan Xiaotao, Foo Willy, Lim Wanrong, Fok Marcus H Y, Liu Ping, Yu Hanry, Maruyama Ichiro, Wohland Thorsten
NUS Graduate Program in Bioengineering, National University of Singapore, 28 Medical Drive, Singapore 117456, Singapore.
Rev Sci Instrum. 2007 May;78(5):053711. doi: 10.1063/1.2740053.
A modified fluorescence correlation microscope (FCM) was built on a commercial confocal laser scanning microscope (CLSM) by adding two sensitive detectors to perform fluorescence correlation spectroscopy (FCS). A single pinhole for both imaging and spectroscopy and a simple slider switch between the two modes thus facilitate the accurate positioning of the FCS observation volume after the confocal image acquisition. Due to the use of a single pinhole for CLSM and FCS the identity of imaged and spectroscopically observed positions is guaranteed. The presented FCM system has the capability to position the FCS observation volume at any point within the inner 30% of the field of view without loss in performance and in the inner 60% of the field of view with changes of FCS parameters of less than 10%. A single pinhole scheme for spatial fluorescence cross correlation spectroscopy performed on the FCM system is proposed to determine microfluidic flow angles. To show the applicability and versatility of the system, we measured the translational diffusion coefficients on the upper and lower membranes of Chinese hamster ovary cells. Two-photon excitation FCS was also realized by coupling a pulsed Ti: sapphire laser into the microscope and used for flow direction characterization in microchannels.
通过在商用共聚焦激光扫描显微镜(CLSM)上添加两个灵敏探测器来构建一台改进型荧光相关显微镜(FCM),以进行荧光相关光谱分析(FCS)。用于成像和光谱分析的单个针孔以及两种模式之间简单的滑动开关,使得在共聚焦图像采集后便于对FCS观测体积进行精确定位。由于CLSM和FCS使用单个针孔,保证了成像位置和光谱观测位置的一致性。所展示的FCM系统能够将FCS观测体积定位在视野内30%的中心区域内的任何点,且性能不受损失;定位在视野内60%的中心区域内时,FCS参数变化小于10%。提出了一种在FCM系统上用于空间荧光交叉相关光谱分析的单针孔方案,以确定微流体流动角度。为展示该系统的适用性和多功能性,我们测量了中国仓鼠卵巢细胞上下膜的平移扩散系数。通过将脉冲钛宝石激光器耦合到显微镜中,还实现了双光子激发FCS,并用于微通道中的流动方向表征。