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Journal Article

Photochemical Properties of the Red-shifted Channelrhodopsin Chrimson

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Lorenz,  Charlotte
Department of Biophysical Chemistry, Max Planck Institute of Biophysics, Max Planck Society;

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Linker,  Stephanie M.
Department of Biophysical Chemistry, Max Planck Institute of Biophysics, Max Planck Society;

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Bamann,  Christian
Department of Biophysical Chemistry, Max Planck Institute of Biophysics, Max Planck Society;

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Citation

Urmann, D., Lorenz, C., Linker, S. M., Braun, M., Wachtveitl, J., & Bamann, C. (2017). Photochemical Properties of the Red-shifted Channelrhodopsin Chrimson. Photochemistry and Photobiology, 93(3), 782-795. doi:https://doi.org/10.1111/php.12741.


Cite as: https://hdl.handle.net/21.11116/0000-0001-1D50-5
Abstract
Color‐tuned variants of channelrhodopsins allow for selective optogenetic manipulation of different host cell populations. Chrimson is the channelrhodopsin with the longest wavelength absorbance maximum. We characterize its photochemical properties at different pH values corresponding to two protonation states of the counterion for the protonated Schiff base. Both states will lead to a functional channel opening, but the route is different as reflected in the photochemical states observed spectroscopically. The light‐induced isomerization kinetics change with the local electrostatic environment, becoming faster with the presence of an anionic counterion. The spectral effect is stronger on the ground‐state energy surface. From the excited state, a bifurcated pathway leads to the electronic ground state resulting in a pronounced excitation wavelength dependence. The subsequent steps in the photocycles at pH 6 and pH 9.5 differ in the accumulation of states with a protonated and deprotonated Schiff base, respectively, that can be correlated with the open channel. Therefore, different protonation states are preserved in the open and the initial states. Chrimson's photocycle at alkaline pH shows features observed in other rhodopsins without an internal proton donor to the Schiff base, but it accumulates an intermediate with an even longer lifetime reflecting slow recovery of the initial state.