4.8 Article

Time-resolved serial crystallography captures high-resolution intermediates of photoactive yellow protein

Journal

SCIENCE
Volume 346, Issue 6214, Pages 1242-1246

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1259357

Keywords

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Funding

  1. NSF [0952643]
  2. NIH [R01GM095583, R24GM111072]
  3. NSF Science and Technology Centers [NSF-1231306]
  4. U.S. Department of Energy by Lawrence Livermore National Laboratory [DE-AC52-07NA27344]
  5. LLNL Lab-Directed Research and Development Project [012-ERD-031]
  6. Direct For Biological Sciences
  7. Div Of Molecular and Cellular Bioscience [1330809] Funding Source: National Science Foundation
  8. Div Of Molecular and Cellular Bioscience
  9. Direct For Biological Sciences [0952643] Funding Source: National Science Foundation
  10. EPSRC [EP/I003304/1] Funding Source: UKRI
  11. Engineering and Physical Sciences Research Council [EP/I003304/1] Funding Source: researchfish

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Serial femtosecond crystallography using ultrashort pulses from x-ray free electron lasers (XFELs) enables studies of the light-triggered dynamics of biomolecules. We used microcrystals of photoactive yellow protein (a bacterial blue light photoreceptor) as a model system and obtained high-resolution, time-resolved difference electron density maps of excellent quality with strong features; these allowed the determination of structures of reaction intermediates to a resolution of 1.6 angstroms. Our results open the way to the study of reversible and nonreversible biological reactions on time scales as short as femtoseconds under conditions that maximize the extent of reaction initiation throughout the crystal.

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