细胞骨架
扫描电镜
中心体
细胞生物学
肌动蛋白
荧光寿命成像显微镜
活体细胞成像
化学
微管蛋白
生物物理学
超分辨显微术
生物
细胞
荧光显微镜
荧光
显微镜
微管
生物化学
光学
受激发射
物理
细胞周期
激光器
作者
Gražvydas Lukinavičius,Luc Reymond,Elisa D’Este,Anastasiya Masharina,Fabian Göttfert,Haisen Ta,Angelika Güther,Mathias Fournier,Stefano Rizzo,Herbert Waldmann,Claudia Blaukopf,Christoph Sommer,Daniel W. Gerlich,Hans‐Dieter Arndt,Stefan W. Hell,Kai Johnsson
出处
期刊:Nature Methods
[Springer Nature]
日期:2014-05-25
卷期号:11 (7): 731-733
被引量:768
摘要
Far-red fluorogenic probes for live-cell imaging of either actin or tubulin are described and used for super-resolution microscopy of various structures in a variety of cell types. We introduce far-red, fluorogenic probes that combine minimal cytotoxicity with excellent brightness and photostability for fluorescence imaging of actin and tubulin in living cells. Applied in stimulated emission depletion (STED) microscopy, they reveal the ninefold symmetry of the centrosome and the spatial organization of actin in the axon of cultured rat neurons with a resolution unprecedented for imaging cytoskeletal structures in living cells.
科研通智能强力驱动
Strongly Powered by AbleSci AI