4.8 Article

Time-resolved serial femtosecond crystallography at the European XFEL

Journal

NATURE METHODS
Volume 17, Issue 1, Pages 73-+

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41592-019-0628-z

Keywords

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Funding

  1. NSF Science and Technology Centers [NSF-1231306]
  2. Gottfried Wilhelm Leibniz Program of the DFG
  3. project 'X-probe' - European Union's 2020 Research and Innovation Program under the Marie Sklodowska-Curie grant [637295]
  4. European Research Council, 'Frontiers in Attosecond X-ray Science: Imaging and Spectroscopy (AXSIS)' [ERC-2013-SyG 609920]
  5. Human Frontiers Science Program grant [RGP0010 2017]
  6. Biodesign Center for Applied Structural Discovery at Arizona State University
  7. NSF award [1565180]
  8. National Institutes of Health [R01GM095583, R01GM117342]
  9. Div Of Biological Infrastructure
  10. Direct For Biological Sciences [1565180] Funding Source: National Science Foundation

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The European XFEL (EuXFEL) is a 3.4-km long X-ray source, which produces femtosecond, ultrabrilliant and spatially coherent X-ray pulses at megahertz (MHz) repetition rates. This X-ray source has been designed to enable the observation of ultrafast processes with near-atomic spatial resolution. Time-resolved crystallographic investigations on biological macromolecules belong to an important class of experiments that explore fundamental and functional structural displacements in these molecules. Due to the unusual MHz X-ray pulse structure at the EuXFEL, these experiments are challenging. Here, we demonstrate how a biological reaction can be followed on ultrafast timescales at the EuXFEL. We investigate the picosecond time range in the photocycle of photoactive yellow protein (PYP) with MHz X-ray pulse rates. We show that difference electron density maps of excellent quality can be obtained. The results connect the previously explored femtosecond PYP dynamics to timescales accessible at synchrotrons. This opens the door to a wide range of time-resolved studies at the EuXFEL. European XFEL allows investigation of the picosecond time range in the photocycle of photoactive yellow protein.

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