Tischer Christian, Hilsenstein Volker, Hanson Kirsten, Pepperkok Rainer
European Molecular Biology Laboratory, Heidelberg, Germany.
Instituto de Medicina Molecular, Lisboa, Portugal.
Methods Cell Biol. 2014;123:489-503. doi: 10.1016/B978-0-12-420138-5.00026-4.
Obtaining sufficient statistics in quantitative fluorescence microscopy is often hampered by the tedious and time-consuming task of manually locating comparable specimen and repeatedly launching the same acquisition protocol. Recent advances in combining fluorescence microscopy with online image analysis tackle this problem by fully integrating the task of identifying and locating the specimen of interest in an automated acquisition workflow. Here, we describe the general requirements and specific microscope control and image analysis software solutions for implementing such automated online feedback microscopy. We demonstrate the power of the method by two selected applications addressing high-throughput 3D imaging of sparsely parasite-infected tissue culture cells and automated fluorescence recovery after photobleaching experiments to quantify the turnover of vesicular coat proteins at ER exit sites.
在定量荧光显微镜中获取足够的统计数据常常受到手动定位可比样本以及反复启动相同采集协议这一繁琐且耗时任务的阻碍。荧光显微镜与在线图像分析相结合的最新进展通过在自动采集工作流程中全面整合识别和定位感兴趣样本的任务来解决这一问题。在此,我们描述了实现这种自动在线反馈显微镜的一般要求以及特定的显微镜控制和图像分析软件解决方案。我们通过两个选定的应用展示了该方法的强大功能,这两个应用分别针对稀疏寄生虫感染的组织培养细胞的高通量3D成像以及光漂白实验后的自动荧光恢复,以量化内质网出口位点囊泡衣被蛋白的周转情况。