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Photoswitching of the chromophore in cerFP505.

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posted on 2013-02-21, 07:33 authored by Alexander Vogt, Cecilia D'Angelo, Franz Oswald, Andrea Denzel, Charles H. Mazel, Mikhail V. Matz, Sergey Ivanchenko, G. Ulrich Nienhaus, Jörg Wiedenmann

A) Absorption spectra after irradiation with 400 nm (on-state) or with 450 nm light (off-state). Deactivation gives rise to a second peak around 390 nm. B) Ground state equilibrium. Irradiation at 400 nm drives the protein to the on-state, 450 nm light turns off the “activatable” fraction of the protein. Bars above the x-axis specify the light treatment, 400 nm light (white bar), 450 nm light (grey bar) or no light (black bar). C) Fluorescence emission of the protein in the on- or off-state was recorded for ≥30 min in the dark after 5 min irradiation with 400 or 450 nm light. Bars above the x-axis specify the light treatment as described above. D) The reversibility of the reaction is shown for eight cycles of activation/deactivation. Bars above the x-axis specify the light treatment as described in (B).

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