4.8 Article

Room temperature femtosecond X-ray diffraction of photosystem II microcrystals

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.1204598109

Keywords

manganese; oxygen-evolving complex

Funding

  1. Office of Science, Office of Basic Energy Sciences (OBES), Division of Chemical Sciences, Geosciences, and Biosciences (CSGB) of the Department of Energy (DOE) [DE-AC02-05CH11231]
  2. Office of Science [DE-AC02-05CH11231]
  3. National Institutes of Health (NIH) [R01-GM095887, GM55302]
  4. Solar Fuels Strong Research Environment (Umea University)
  5. Artificial Leaf Project (K&Wallenberg Foundation)
  6. Vetenskapsradet
  7. Alexander von Humboldt Foundation
  8. LCLS
  9. Atomic, Molecular and Optical Sciences Program
  10. CSGB Division, OBES, DOE
  11. SLAC Laboratory Directed Research and Development Program
  12. DOE OBES
  13. National Center for Research Resources
  14. DOE Office of Biological and Environmental Research

Ask authors/readers for more resources

Most of the dioxygen on earth is generated by the oxidation of water by photosystem II (PS II) using light from the sun. This lightdriven, four-photon reaction is catalyzed by the Mn4CaO5 cluster located at the lumenal side of PS II. Various X-ray studies have been carried out at cryogenic temperatures to understand the intermediate steps involved in the water oxidation mechanism. However, the necessity for collecting data at room temperature, especially for studying the transient steps during the O-O bond formation, requires the development of new methodologies. In this paper we report room temperature X-ray diffraction data of PS II microcrystals obtained using ultrashort (<50 fs) 9 keV X-ray pulses from a hard X-ray free electron laser, namely the Linac Coherent Light Source. The results presented here demonstrate that the probe before destroy approach using an X-ray free electron laser works even for the highly-sensitive Mn4CaO5 cluster in PS II at room temperature. We show that these data are comparable to those obtained in synchrotron radiation studies as seen by the similarities in the overall structure of the helices, the protein subunits and the location of the various cofactors. This work is, therefore, an important step toward future studies for resolving the structure of the Mn4CaO5 cluster without any damage at room temperature, and of the reaction intermediates of PS II during O-O bond formation.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available