Attenuation of photobleaching in two-photon excitation fluorescence from green fluorescent protein with shaped excitation pulses

2003 ◽  
Vol 311 (3) ◽  
pp. 592-596 ◽  
Author(s):  
Hiroyuki Kawano ◽  
Yasuo Nabekawa ◽  
Akira Suda ◽  
Yu Oishi ◽  
Hideaki Mizuno ◽  
...  
2002 ◽  
Vol 291 (5) ◽  
pp. 1272-1275 ◽  
Author(s):  
Tong-Sheng Chen ◽  
Shao-Qun Zeng ◽  
Qing-Ming Luo ◽  
Zhi-Hong Zhang ◽  
Wei Zhou

ChemPhysChem ◽  
2006 ◽  
Vol 7 (1) ◽  
pp. 250-260 ◽  
Author(s):  
Mircea Cotlet ◽  
Peter M. Goodwin ◽  
Geoffrey S. Waldo ◽  
James H. Werner

2005 ◽  
Vol 217 (3) ◽  
pp. 200-204 ◽  
Author(s):  
E. SPIESS ◽  
F. BESTVATER ◽  
A. HECKEL-POMPEY ◽  
K. TOTH ◽  
M. HACKER ◽  
...  

2007 ◽  
Vol 15 (3) ◽  
pp. 3-5
Author(s):  
Stephen W. Carmichael

How do lumens form? Two mechanisms that come readily to mind are a wrapping model, similar to the wrapping of the myelin sheath around a neuronal process, and a solid core of cells followed by apoptosis of the central cells. Another obvious mechanism that was suggested over 100 years ago is the fusion of intracellular vacuoles. Whereas several recent studies have supported this latter mechanism, it has not yet been proven. Now, the appropriate animal model (zebrafish), the modern techniques (transgenic chimeras), dyes (green fluorescent protein and monomeric red fluorescent protein) that can be linked to proteins to label vacuoles, and two-photon imaging in real time finally have provided the strongest support yet. In an article by Makoto Kamei, Brian Saunders, Kayla Bayless, Louis Dye, George Davis, and Brant Weinstein the assembly of endothelial tubes from intracellular vacuoles was observed in vitro and in vivo.


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