4.8 Article

Membrane protein megahertz crystallography at the European XFEL

Journal

NATURE COMMUNICATIONS
Volume 10, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-019-12955-3

Keywords

-

Funding

  1. Biodesign Center for Applied Structural Discovery at Arizona State University
  2. National Science Foundation (NSF) Science awards for Technology Center (STC) BioXFEL [STC1231306, 1565180]
  3. U.S. Department of Energy, Office of Science, Basic Energy Sciences [DE-SC0002164, DE-SC0010575]
  4. National Institutes of Health [R01GM095583]
  5. AXSIS project - European Research Council under the European Union [609920]
  6. excellence cluster The Hamburg Center for Ultrafast Imaging-Structure, Dynamics, and Control of Matter at the Atomic Scale of the Deutsche Forschungsgemeinschaft (CUI) [DFG-EXC1074]
  7. BMBF through the Roentgen-Angstrom Cluster grant [05K18CHA]
  8. U.S. Department of Energy by Lawrence Livermore National Laboratory [DE-AC52-07NA27344]
  9. NIH [R01GM117342]
  10. Australian Research Council through the Centre of Excellence in Advanced Molecular Imaging [CE140100011]
  11. European Research Council (ERC) [609920] Funding Source: European Research Council (ERC)
  12. U.S. Department of Energy (DOE) [DE-SC0010575] Funding Source: U.S. Department of Energy (DOE)

Ask authors/readers for more resources

The world's first superconducting megahertz repetition rate hard X-ray free-electron laser (XFEL), the European XFEL, began operation in 2017, featuring a unique pulse train structure with 886 ns between pulses. With its rapid pulse rate, the European XFEL may alleviate some of the increasing demand for XFEL beamtime, particularly for membrane protein serial femtosecond crystallography (SFX), leveraging orders-of-magnitude faster data collection. Here, we report the first membrane protein megahertz SFX experiment, where we determined a 2.9 angstrom-resolution SFX structure of the large membrane protein complex, Photosystem I, a > 1 MDa complex containing 36 protein subunits and 381 cofactors. We address challenges to megahertz SFX for membrane protein complexes, including growth of large quantities of crystals and the large molecular and unit cell size that influence data collection and analysis. The results imply that megahertz crystallography could have an important impact on structure determination of large protein complexes with XFELs.

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