Targeted green-red photoconversion of EosFP, a fluorescent marker protein

被引:27
作者
Ivanchenko, S
Röcker, C
Oswald, F
Wiedenmann, J
Nienhaus, GU
机构
[1] Univ Ulm, Dept Biophys, D-89069 Ulm, Germany
[2] Univ Ulm, Dept Internal Med 1, D-89070 Ulm, Germany
[3] Univ Ulm, Dept Gen Zool & Endocrinol, D-89070 Ulm, Germany
[4] Univ Illinois, Dept Phys, Urbana, IL 61801 USA
关键词
fluorescent protein; fusion protein; two-photon excitation; fluorescence spectroscopy; photoconversion; GFP-LIKE PROTEINS; LIVING CELLS; CORRELATION SPECTROSCOPY; ANTHOZOA; EXCITATION; CORAL; NONBIOLUMINESCENT; OLIGOMERIZATION; MITOCHONDRIA; CONVERSION;
D O I
10.1007/s10867-005-0174-z
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
EosFP is a novel fluorescent protein from the stony coral Lobophyllia hemprichii. Its gene was cloned in Escherichia coli to express the tetrameric wild-type protein. The protein emits strong green fluorescence (516 nm) that shifts toward red (581 nm) upon near-ultraviolet irradiation at similar to 390 nm due to a photo-induced modification that involves a break in the peptide backbone next to the chromophore. Using site-directed mutagenesis, dimeric (d1EosFP, d2EosFP) and monomeric (mEosFP) variants were produced with essentially unaltered spectroscopic properties. Here we present a spectroscopic characterization of EosFP and its variants, including room- and low-temperature spectra, fluorescence lifetime determinations, two-photon excitation and two-photon photoconversion. Furthermore, by transfection of a human cancer (HeLa) cell with a fusion construct of a mitochondrial targeting sequence and d2EosFP, we demonstrate how localized photoconversion of EosFP can be employed for resolving intracellular processes.
引用
收藏
页码:249 / 259
页数:11
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