Ultrafast, remote-controlled protonation reaction enables structural changes in a phytochrome

In photoactive proteins, coupling between the chromophore and protein matrix is exquisitely tuned. Proton transfer reactions can mediate this coupling, as in proton-coupled electron transfer and excited-state proton transfer. Additional mechanisms involving proton dislocations may exist but remain undiscovered. Here, we present a femtosecond crystallographic movie of the phytochrome from <i>Deinococcus radiodurans</i>. The structures reveal a space-conserving mechanism for rotation of the D-ring in the excited state. We observe rearrangement of a conserved hydrogen bond network within 300 fs, which precedes the isomerization reaction of the chromophore. Aided by molecular modeling and independently confirmed by femtosecond infrared spectroscopy, we attribute these changes to a protonation shift of the strictly conserved histidine-260. Although this histidine lies close to the photoexcited π-orbitals of the chromophore, it is not directly part of them. We propose that this "remote-controlled" proton transfer relays photoexcitation near-instantaneously to the protein matrix. This mechanism may be widely used to transduce cofactor signals to their hosting enzymes.

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Journal
Science Advances
Published
2025-10-17
DOI
https://doi.org/10.1126/sciadv.ady0499
Citations
1
Primary Topic
Photosynthetic Processes and Mechanisms
Type
article
Field-Weighted Citation Impact
0.81
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article

Ultrafast, remote-controlled protonation reaction enables structural changes in a phytochrome

Emina A. Stojković, Suraj Pandey, Atsarina Larasati Anindya, Marius Schmidt et al.
1 citations
Science Advances
Photosynthetic Processes and Mechanisms
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article

Ultrafast, remote-controlled protonation reaction enables structural changes in a phytochrome

Emina A. Stojković, Suraj Pandey, Atsarina Larasati Anindya, Marius Schmidt, Janne A. Ihalainen, Amke Nimmrich, Takehiko Tosha, Elin Claesson, Tatu Kumpulainen, Piotr Maj, Lukas Grunewald, Fangjia Luo, Moona Kurttila, Dmitry I. Morozov, Brigitte Stucki-Buchli, Giacomo Salvadori, Weixiao Yuan Wahlgren, Kensuke Tono, S. Madan Kumar, Rie Tanaka, Shigeki Owada, Andrea Cellini, Sebastian Westenhoff, Tek Narsingh Malla, Heikki Takala, Pasi Myllyperkiö, Anna-Lena M. Fischer, Nuemket Nipawan
article en
1 citations

Abstract

In photoactive proteins, coupling between the chromophore and protein matrix is exquisitely tuned. Proton transfer reactions can mediate this coupling, as in proton-coupled electron transfer and excited-state proton transfer. Additional mechanisms involving proton dislocations may exist but remain undiscovered. Here, we present a femtosecond crystallographic movie of the phytochrome from <i>Deinococcus radiodurans</i>. The structures reveal a space-conserving mechanism for rotation of the D-ring in the excited state. We observe rearrangement of a conserved hydrogen bond network within 300 fs, which precedes the isomerization reaction of the chromophore. Aided by molecular modeling and independently confirmed by femtosecond infrared spectroscopy, we attribute these changes to a protonation shift of the strictly conserved histidine-260. Although this histidine lies close to the photoexcited π-orbitals of the chromophore, it is not directly part of them. We propose that this "remote-controlled" proton transfer relays photoexcitation near-instantaneously to the protein matrix. This mechanism may be widely used to transduce cofactor signals to their hosting enzymes.

Science AdvancesVol. 11(42)
Thammasat University (TH), Uppsala University (SE), Jagiellonian University (PL), Forschungszentrum Jülich (DE), University of Washington (US), Kyoto University (JP), Northeastern Illinois University (US), Science for Life Laboratory (SE), SPring-8 (JP), Japan Synchrotron Radiation Research Institute (JP), Frederick National Laboratory for Cancer Research (US), University of Wisconsin–Milwaukee (US), University of Gothenburg (SE), University of Jyväskylä (FI)
Openalex Percentile: Top 22%
Photosynthetic Processes and Mechanisms
0.81
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