Single molecule spectroscopic characterization of GFP-MUT2 mutant for two-photon microscopy applications

被引:18
|
作者
Cannone, F
Caccia, M
Bologna, S
Diaspro, A
Chirico, G
机构
[1] Univ Genoa, Dipartimento Fis, MicroScoBio, I-16146 Genoa, Italy
[2] LAMBS, Genoa, Italy
[3] Univ Milano Bicocca, Dipartimento Fis, I-20126 Milan, Italy
[4] Univ Parma, Dept Biochem & Mol Biol, I-43100 Parma, Italy
[5] Ist Nazl Fis Materia, I-16152 Genoa 24, Italy
关键词
two-photon microscopy; GFP; fluorescence; photobleaching;
D O I
10.1002/jemt.20125
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Green Fluorescent Protein (GFP) mutants are extensively used in optical microscopy studies of in vivo biological processes in cells. Nonetheless, blinking and bleaching of the GFP chromophore at the single molecule level greatly limits its usefulness. We have worked out what we think are the best experimental conditions for the use of the GFP mutant, GFP-mut2, as a single molecule marker in two-photon excitation measurements. We have measured molecular brightness, excited state lifetime, blinking and photo-bleaching times versus the two-photon excitation intensity on proteins embedded in silica gel matrices versus the excitation wavelength in the range 700-1,000 nm. Our results indicate that GFPmut2 can be employed as a long-lived reporter of biological processes. (C) 2005 Wiley-Liss, Inc.
引用
收藏
页码:186 / 193
页数:8
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