Shevchuk Andrew I, Hobson Phil, Lab Max J, Klenerman David, Krauzewicz Nina, Korchev Yuri E
MRC Clinical Sciences Centre, Faculty of Medicine, Imperial College London, Hammersmith Hospital Campus, Du Cane Road, London W12 0NN, UK.
Pflugers Arch. 2008 Apr;456(1):227-35. doi: 10.1007/s00424-007-0410-4. Epub 2008 Jan 5.
We introduce a novel high resolution scanning surface confocal microscopy technique that enables imaging of endocytic pits in apical membranes of live cells for the first time. The improved topographical resolution of the microscope together with simultaneous fluorescence confocal detection produces pairs of images of cell surfaces sufficient to identify single endocytic pits. Whilst the precise position and size of the pit is detected by the ion conductance microscope, the molecular nature of the pit, e.g. clathrin coated or caveolae, is determined by the corresponding green fluorescent protein fluorescence. Also, for the first time, we showed that flotillin 1 and 2 can be found co-localising with approximately 200-nm indentations in the cell membrane that supports involvement of this protein in endocytosis.
我们引入了一种新型的高分辨率扫描表面共聚焦显微镜技术,该技术首次能够对活细胞顶端膜中的内吞小窝进行成像。显微镜改进后的形貌分辨率与同步荧光共聚焦检测相结合,生成了足以识别单个内吞小窝的细胞表面图像对。虽然小窝的精确位置和大小由离子传导显微镜检测,但小窝的分子性质,如网格蛋白包被的或小窝的,由相应的绿色荧光蛋白荧光确定。此外,我们首次表明,浮舰蛋白1和2可与细胞膜中约200纳米的凹陷共定位,这支持了该蛋白参与内吞作用。