Characterization of an improved donor fluorescent protein for Forster resonance energy transfer microscopy

被引:61
作者
Day, Richard N. [1 ,2 ]
Booker, Cynthia F. [1 ,2 ]
Periasamy, Ammasi [3 ,4 ]
机构
[1] Univ Virginia Hlth Syst, Dept Med, Charlottesville, VA 22908 USA
[2] Univ Virginia Hlth Syst, Dept Cell Biol, Charlottesville, VA 22908 USA
[3] Univ Virginia, WM Keck Ctr Cellular Imaging, Dept Biol, Charlottesville, VA 22904 USA
[4] Univ Virginia, WM Keck Ctr Cellular Imaging, Dept Biomed Engn, Charlottesville, VA 22904 USA
关键词
Forster resonance energy transfer microscopy; live cell imaging; fluorescent proteins; Teal fluorescent protein; Cerulean; Venus; protein-protein interactions;
D O I
10.1117/1.2939094
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The genetically encoded fluorescent proteins (FP), used in combination with Forster resonance energy transfer (FRET) microscopy, provide the tools necessary for the direct visualization of protein interactions inside living cells. Typically, the Cerulean and Venus variants of the cyan and yellow FPS are used for FRET studies, but there are limitations to their use. Here, Cerulean and the newly developed monomeric Teal FP (mTFP) are compared as FRET donors for Venus using spectral and fluorescence lifetime measurements from living cells. The results demonstrate that when compared to Cerulean, mTFP has increased brightness, optimal excitation using the standard 458-nm laser line, increased photostability, and improved spectral overlap with Venus. In addition, the two-photon excitation and fluorescence lifetime characteristics are determined for mTFP. Together, these measurements indicate that mTFP is an excellent donor fluorophore for FRET studies, and that its use may improve the detection of interactions involving proteins that are difficult to express, or that need to be produced at low levels in cells. (c) 2008 Society of Photo-Optical Instrumentation Engineers.
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页数:9
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