Lechtreck Karl F
Department of Cellular Biology, University of Georgia, 635 Biological Science Building, 1000 Cedar Street, Athens, GA, 30602, USA.
Methods Mol Biol. 2016;1454:83-96. doi: 10.1007/978-1-4939-3789-9_6.
The assembly of cilia and eukaryotic flagella (interchangeable terms) requires the import of numerous proteins from the cell body into the growing organelle. Proteins move into and inside cilia by diffusion and by motor-based intraflagellar transport (IFT). Many aspects of ciliary protein transport such as the distribution of unloading sites and the frequency of transport can be analyzed using direct in vivo imaging of fluorescently tagged proteins. Here, we will describe how to use total internal reflection fluorescence microcopy (TIRFM) to analyze protein transport in the flagella of the unicellular alga Chlamydomonas reinhardtii, a widely used model for cilia and cilia-related disease.
纤毛与真核生物鞭毛(这两个术语可互换使用)的组装需要将大量蛋白质从细胞体导入正在生长的细胞器中。蛋白质通过扩散以及基于马达蛋白的鞭毛内运输(IFT)进入纤毛并在其中移动。利用荧光标记蛋白的直接体内成像技术,可以分析纤毛蛋白运输的许多方面,如卸载位点的分布和运输频率。在这里,我们将描述如何使用全内反射荧光显微镜(TIRFM)来分析单细胞藻类莱茵衣藻鞭毛中的蛋白质运输,莱茵衣藻是一种广泛用于研究纤毛及纤毛相关疾病的模型。