Nature Communications (Nov 2024)

Structural effects of high laser power densities on an early bacteriorhodopsin photocycle intermediate

  • Quentin Bertrand,
  • Przemyslaw Nogly,
  • Eriko Nango,
  • Demet Kekilli,
  • Georgii Khusainov,
  • Antonia Furrer,
  • Daniel James,
  • Florian Dworkowski,
  • Petr Skopintsev,
  • Sandra Mous,
  • Isabelle Martiel,
  • Per Börjesson,
  • Giorgia Ortolani,
  • Chia-Ying Huang,
  • Michal Kepa,
  • Dmitry Ozerov,
  • Steffen Brünle,
  • Valerie Panneels,
  • Tomoyuki Tanaka,
  • Rie Tanaka,
  • Kensuke Tono,
  • Shigeki Owada,
  • Philip J. M. Johnson,
  • Karol Nass,
  • Gregor Knopp,
  • Claudio Cirelli,
  • Christopher Milne,
  • Gebhard Schertler,
  • So Iwata,
  • Richard Neutze,
  • Tobias Weinert,
  • Jörg Standfuss

DOI
https://doi.org/10.1038/s41467-024-54422-8
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 11

Abstract

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Abstract Time-resolved serial crystallography at X-ray Free Electron Lasers offers the opportunity to observe ultrafast photochemical reactions at the atomic level. The technique has yielded exciting molecular insights into various biological processes including light sensing and photochemical energy conversion. However, to achieve sufficient levels of activation within an optically dense crystal, high laser power densities are often used, which has led to an ongoing debate to which extent photodamage may compromise interpretation of the results. Here we compare time-resolved serial crystallographic data of the bacteriorhodopsin K-intermediate collected at laser power densities ranging from 0.04 to 2493 GW/cm2 and follow energy dissipation of the absorbed photons logarithmically from picoseconds to milliseconds. Although the effects of high laser power densities on the overall structure are small, in the upper excitation range we observe significant changes in retinal conformation and increased heating of the functionally critical counterion cluster. We compare light-activation within crystals to that in solution and discuss the impact of the observed changes on bacteriorhodopsin biology.