| Literature DB >> 27731796 |
Artem Y Lyubimov1,2,3,4,5, Monarin Uervirojnangkoorn1,2,4,3,5, Oliver B Zeldin1,2,4,3,5, Qiangjun Zhou1,2,4,3,5, Minglei Zhao1,2,4,3,5, Aaron S Brewster6, Tara Michels-Clark6, James M Holton6,7,8, Nicholas K Sauter6, William I Weis1,3,4, Axel T Brunger1,2,4,3,5.
Abstract
X-ray free electron lasers (XFELs) reduce the effects of radiation damage on macromolecular diffraction data and thereby extend the limiting resolution. Previously, we adapted classical post-refinement techniques to XFEL diffraction data to produce accurate diffraction data sets from a limited number of diffraction images (Uervirojnangkoorn et al., 2015), and went on to use these techniques to obtain a complete data set from crystals of the synaptotagmin-1 / SNARE complex and to determine the structure at 3.5 Å resolution (Zhou et al., 2015). Here, we describe new advances in our methods and present a reprocessed XFEL data set of the synaptotagmin-1 / SNARE complex. The reprocessing produced small improvements in electron density maps and the refined atomic model. The maps also contained more information than those of a lower resolution (4.1 Å) synchrotron data set. Processing a set of simulated XFEL diffraction images revealed that our methods yield accurate data and atomic models.Entities:
Keywords: X-ray free electron laser; biophysics; macromolecular crystallography; post-refinement; radiation damage; structural biology
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Year: 2016 PMID: 27731796 PMCID: PMC5094853 DOI: 10.7554/eLife.18740
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140