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Single molecule fluorescence imaging of the photoinduced conversion and bleaching behavior of the fluorescent protein Kaede
Author(s) -
Schäfer S.P.,
Dittrich P.S.,
Petrov E.P.,
Schwille P.
Publication year - 2006
Publication title -
microscopy research and technique
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.536
H-Index - 118
eISSN - 1097-0029
pISSN - 1059-910X
DOI - 10.1002/jemt.20283
Subject(s) - fluorescence , chemistry , biophysics , photochemistry , molecule , fluorescent protein , green fluorescent protein , biochemistry , biology , optics , organic chemistry , gene , physics
Photoconversion and photobleaching behavior of the fluorescent protein Kaede immobilized in polyacrylamide gel matrix at room temperature was studied by single molecule wide‐field fluorescence microscopy. Photobleaching kinetics of Kaede molecules upon excitation at 488 nm showed slight heterogeneity, suggesting the presence of different protein conformations and/or the distribution of local environments in the gel matrix. Statistical analysis of intensity trajectories of single molecules revealed four major types of fluorescence dynamics behavior upon short illumination by a violet light pulse (405 nm). In particular, two types of photoswitching behavior were observed: the green‐to‐red photoconversion (4% of Kaede molecules) and the photoactivation of green fluorescence without emission of red fluorescence (13%). Two other major groups show neither photoconversion nor red emission and demonstrate photoinduced partial deactivation (43%) and partial revival (30%) of green fluorescence. The significantly lower green‐to‐red conversion ratio as compared with bulk measurements in aqueous solution might be induced by the immobilization of the protein molecules within a polyacrylamide gel. Contrary to Ando et al. (Proc Natl Acad Sci 2002;99:12651–12656), we found a significant increase in green fluorescence emission upon illumination with 405‐nm light, which is typical for GFP and related proteins. Microsc. Res. Tech. 69: 210–219, 2006. © 2006 Wiley‐Liss, Inc.