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用于分析盘基网柄菌微管的活细胞成像技术。

Live cell-imaging techniques for analyses of microtubules in Dictyostelium.

作者信息

Samereier Matthias, Meyer Irene, Koonce Michael P, Gräf Ralph

机构信息

Department of Cell Biology, Institut for Biochemistry and Biology, University of Potsdam, Potsdam-Golm 27708, Germany D-14476.

出版信息

Methods Cell Biol. 2010;97:341-57. doi: 10.1016/S0091-679X(10)97018-0.

Abstract

Dictyostelium amoebae provide a popular model system for analyses of cell and cytoskeletal dynamics. Yet, the sensitivity of Dictyostelium cells to phototoxic effects, their rapid cell movement, and the extraordinary motility of their microtubule system are specific challenges for live cell imaging. The protocols outlined in this chapter are optimized to minimize these challenges, using Dictyostelium cells expressing green fluorescent tubulin or microtubule plus-end markers such as TACC. We describe suitable specimen preparations, treatments with microtubule-depolymerizing drugs, and applicable settings on wide-field and confocal microscopy systems for four-dimensional time-lapse and fluorescence recovery after photobleaching analyses of microtubule dynamics.

摘要

盘基网柄菌变形虫为细胞和细胞骨架动力学分析提供了一个常用的模型系统。然而,盘基网柄菌细胞对光毒性效应的敏感性、其快速的细胞运动以及微管系统的非凡运动性,对于活细胞成像来说是特定的挑战。本章概述的方案经过优化,以尽量减少这些挑战,使用表达绿色荧光微管蛋白或微管正端标记物(如TACC)的盘基网柄菌细胞。我们描述了合适的样本制备方法、用微管解聚药物进行的处理,以及在宽视野和共聚焦显微镜系统上用于微管动力学的四维延时和光漂白后荧光恢复分析的适用设置。

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