4.8 Article

L-Edge X-ray Absorption Spectroscopy of Dilute Systems Relevant to Metalloproteins Using an X-ray Free-Electron Laser

期刊

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
卷 4, 期 21, 页码 3641-3647

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jz401837f

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资金

  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-AC02-050CH11231]
  2. LBNL Laboratory Directed Research and Development award
  3. NIH [GM50781, GM055302]
  4. Alexander von Humboldt Foundation
  5. Ruth L. Kirschstein National Research Service Award [F32GM100595]
  6. OBES
  7. CSGB of the DOE [DE-AC02-76SF00515]
  8. LCLS
  9. SLAC Laboratory Directed Research and Development award
  10. Volkswagenstiftung Peter Paul Ewald fellowship
  11. Swedish Energy Agency (Energimyn-digheten)
  12. K&A Wallenberg Foundation (Artificial Leaf Umea)
  13. Umea University (Solar Fuels Umea)
  14. Stanford University through the Stanford Institute for Materials Energy Sciences (SIMES)
  15. Lawrence Berkeley National Laboratory (LBNL), University of Hamburg through the BMBF priority program [FSP 301]
  16. Center for Free Electron Laser Science (CFEL)
  17. BMBF project Next generation instrumentation for ultrafast X-ray science at accelerator-driven photon source [05K12CB4]
  18. Helmholtz Virtual Institute Dynamic Pathways in Multidimensional Landscapes
  19. European Community [PCIG10-GA-2011-297905]
  20. [SFB755-DFG]

向作者/读者索取更多资源

L-edge spectroscopy of 3d transition metals provides important electronic structure information and has been used in many fields. However, the use of this method for studying dilute aqueous systems, such as metalloenzymes, has not been prevalent because of severe radiation damage and the lack of suitable detection systems. Here we present spectra from a dilute Mn aqueous solution using a high-transmission zone-plate spectrometer at the Linac Coherent Light Source (LCLS). The spectrometer has been optimized for discriminating the Mn L-edge signal from the overwhelming 0 K-edge background that arises from water and protein itself, and the ultrashort LCLS X-ray pulses can outrun X-ray induced damage. We show that the deviations of the partial-fluorescence yield-detected spectra from the true absorption can be well modeled using the state-dependence of the fluorescence yield, and discuss implications for the application of our concept to biological samples.

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