Live-cell super-resolution imaging with trimethoprim conjugates

被引:0
|
作者
Wombacher R. [1 ,5 ]
Heidbreder M. [2 ]
Van De Linde S. [3 ]
Sheetz M.P. [4 ]
Heilemann M. [2 ]
Cornish V.W. [1 ]
Sauer M. [3 ]
机构
[1] Department of Chemistry, Columbia University, New York, NY
[2] Applied Laser Physics and Laser Spectroscopy, Bielefeld University, Bielefeld
[3] Department of Biotechnology and Biophysics, Julius Maximilians University Wuerzburg, Wuerzburg
[4] Department of Biological Sciences, Columbia University, New York, NY
[5] Institute of Pharmacy and Molecular Biotechnology, Heidelberg University, Heidelberg
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nmeth.1489
中图分类号
学科分类号
摘要
The spatiotemporal resolution of subdiffraction fluorescence imaging has been limited by the difficulty of labeling proteins in cells with suitable fluorophores. Here we report a chemical tag that allows proteins to be labeled with an organic fluorophore with high photon flux and fast photoswitching performance in live cells. This label allowed us to image the dynamics of human histone H2B protein in living cells at ∼20 nm resolution. © 2010 Nature America, Inc. All rights reserved.
引用
收藏
页码:717 / 719
页数:2
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