Evidence map›Paper›PMID 30821711›Full record

ArticleActa crystallographica. Section D, Structural biology2019

Resolving indexing ambiguities in X-ray free-electron laser diffraction patterns.

Monarin Uervirojnangkoorn, Artem Y Lyubimov, Qiangjun Zhou, William I Weis, Axel T Brunger

Abstract read
In one paragraph

Article in Acta crystallographica. Section D, Structural biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Monarin UervirojnangkoornLinac Coherent Light Source, SLAC National Accelerator Laboratory, Menlo Park, CA 94025, USA.
Artem Y LyubimovStanford Synchrotron Radiation Laboratory, SLAC National Accelerator Laboratory, Menlo Park, CA 94025, USA.
Qiangjun ZhouDepartment of Molecular and Cellular Physiology, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0003-1789-9588
William I WeisDepartment of Molecular and Cellular Physiology, Stanford University, Stanford, CA 94305, USA.
Axel T BrungerLinac Coherent Light Source, SLAC National Accelerator Laboratory, Menlo Park, CA 94025, USA.ORCID 0000-0001-5121-2036

Funding

Molecular Mechanism and Regulation of Asynchronous ReleaseR00MH113764 · NIMH · VANDERBILT UNIVERSITY · PI ZHOU, QIANGJUN · 2020 to 2022
$719k
Molecular Mechanism and Regulation of Asynchronous ReleaseK99MH113764 · NIMH · STANFORD UNIVERSITY · PI ZHOU, QIANGJUN · 2017 to 2018
$223k
NIMH NIH HHS K99 MH113764NIMH NIH HHS R00 MH113764
6 · The paper itself

Abstract

Processing X-ray free-electron laser (XFEL) diffraction images poses challenges, as an XFEL pulse is powerful enough to destroy or damage the diffracting volume and thereby yields only one diffraction image per volume. Moreover, the crystal is stationary during the femtosecond pulse, so reflections are generally only partially recorded. Therefore, each XFEL diffraction image must be scaled individually and, ideally, corrected for partiality prior to merging. An additional complication may arise owing to indexing ambiguities when the symmetry of the Bravais lattice is higher than that of the space group, or when the unit-cell dimensions are similar to each other. Here, an automated method is presented that diagnoses these indexing ambiguities based on the Brehm-Diederichs algorithm [Brehm & Diederichs (2014), Acta Cryst. D70, 101-109] and produces a consistent indexing choice for the large majority of diffraction images. This method was applied to an XFEL diffraction data set measured from crystals of the neuronal SNARE-complexin-1-synaptotagmin-1 complex. After correcting the indexing ambiguities, substantial improvements were observed in the merging statistics and the atomic model refinement R values. This method should be a useful addition to the arsenal of tools for the processing of XFEL diffraction data sets.

Indexed as

Adaptor Proteins, Vesicular TransportAlgorithmsAnimalsData CollectionElectronsLasersModels, MolecularNerve Tissue ProteinsRatsSNARE ProteinsSynaptotagmin ISynchrotronsX-Ray DiffractionAdaptor Proteins, Vesicular Transportcomplexin INerve Tissue ProteinsSNARE ProteinsSynaptotagmin ISyt1 protein, ratindexing ambiguityserial crystallographyXFELs

Identifiers

PMID30821711
PMCPMC6400252

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.