Photoinduced Interactions in a Pyrene-Calix[4]arene-Perylene Bisimide Dye  System: Probing Ground-State Conformations with Excited-State Dynamics of  Charge Separation and Recombination - The Journal of Physical Chemistry C

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IJMS - Free Full-Text - Ultrafast Photoconversion Dynamics of the Knotless  Phytochrome SynCph2 - HTML

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Open Gain Access To, Post 1 Institute of Physical and Theoretical Chemistry, Goethe University Frankfurt am Main, Max-von-Laue Strae 7, 60438 Frankfurt, Germany 2 Institute of Biophysics, Goethe University Frankfurt am Main, Max-von-Laue Strae 1, 60438 Frankfurt, Germany 3 Department of Chemistry, Philipps-Universitt Marburg, Hans-Meerwein-Strae 4, 35032 Marburg, Germany 4 Center for Synthetic Microbiology, Philipps-Universitt Marburg, Hans-Meerwein-Strae 6, 35032 Marburg, Germany * Authors to whom correspondence should be resolved.

Knotless phytochromes are among the three main subgroups classified by their distinct lack of the PAS domain in their photosensory core module, which is in contrast to the canonical PAS-GAF-PHY range. In spite of intensive research study on the ultrafast photodynamics of phytochromes, little is understood about the primary kinetics in knotless phytochromes.

Our outcomes reveal that the ecstatic state life time of Pr * (200 ps) is comparable to bacteriophytochromes, however a lot longer than in a lot of canonical phytochromes.  Answers Shown Here  assign the slow Pr * kinetics to relaxation processes of the chromophore-binding pocket that controls the bilin chromophore's isomerization step. The Pfr photoconversion dynamics begins with a faster thrilled state relaxation than in canonical phytochromes, but, despite the differences in the particular domain architectures, continues through similar ground state intermediate steps up to Meta-F.

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e., offered area and flexibility) within the binding pocket, while the general response actions following the photoexcitation are more than likely conserved amongst the red/far-red phytochromes.

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