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Protein crystal structure from non-oriented, single-axis sparse X-ray data

X-ray free-electron lasers (XFELs) have inspired the development of serial femtosecond crystallography (SFX) as a method to solve the structure of proteins. SFX datasets are collected from a sequence of protein microcrystals injected across ultrashort X-ray pulses. The idea behind SFX is that diffra...

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Autores principales: Wierman, Jennifer L., Lan, Ti-Yen, Tate, Mark W., Philipp, Hugh T., Elser, Veit, Gruner, Sol M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4704078/
https://www.ncbi.nlm.nih.gov/pubmed/26870380
http://dx.doi.org/10.1107/S2052252515018795
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author Wierman, Jennifer L.
Lan, Ti-Yen
Tate, Mark W.
Philipp, Hugh T.
Elser, Veit
Gruner, Sol M.
author_facet Wierman, Jennifer L.
Lan, Ti-Yen
Tate, Mark W.
Philipp, Hugh T.
Elser, Veit
Gruner, Sol M.
author_sort Wierman, Jennifer L.
collection PubMed
description X-ray free-electron lasers (XFELs) have inspired the development of serial femtosecond crystallography (SFX) as a method to solve the structure of proteins. SFX datasets are collected from a sequence of protein microcrystals injected across ultrashort X-ray pulses. The idea behind SFX is that diffraction from the intense, ultrashort X-ray pulses leaves the crystal before the crystal is obliterated by the effects of the X-ray pulse. The success of SFX at XFELs has catalyzed interest in analogous experiments at synchrotron-radiation (SR) sources, where data are collected from many small crystals and the ultrashort pulses are replaced by exposure times that are kept short enough to avoid significant crystal damage. The diffraction signal from each short exposure is so ‘sparse’ in recorded photons that the process of recording the crystal intensity is itself a reconstruction problem. Using the EMC algorithm, a successful reconstruction is demonstrated here in a sparsity regime where there are no Bragg peaks that conventionally would serve to determine the orientation of the crystal in each exposure. In this proof-of-principle experiment, a hen egg-white lysozyme (HEWL) crystal rotating about a single axis was illuminated by an X-ray beam from an X-ray generator to simulate the diffraction patterns of microcrystals from synchrotron radiation. Millions of these sparse frames, typically containing only ∼200 photons per frame, were recorded using a fast-framing detector. It is shown that reconstruction of three-dimensional diffraction intensity is possible using the EMC algorithm, even with these extremely sparse frames and without knowledge of the rotation angle. Further, the reconstructed intensity can be phased and refined to solve the protein structure using traditional crystallographic software. This suggests that synchrotron-based serial crystallography of micrometre-sized crystals can be practical with the aid of the EMC algorithm even in cases where the data are sparse.
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spelling pubmed-47040782016-02-11 Protein crystal structure from non-oriented, single-axis sparse X-ray data Wierman, Jennifer L. Lan, Ti-Yen Tate, Mark W. Philipp, Hugh T. Elser, Veit Gruner, Sol M. IUCrJ Research Papers X-ray free-electron lasers (XFELs) have inspired the development of serial femtosecond crystallography (SFX) as a method to solve the structure of proteins. SFX datasets are collected from a sequence of protein microcrystals injected across ultrashort X-ray pulses. The idea behind SFX is that diffraction from the intense, ultrashort X-ray pulses leaves the crystal before the crystal is obliterated by the effects of the X-ray pulse. The success of SFX at XFELs has catalyzed interest in analogous experiments at synchrotron-radiation (SR) sources, where data are collected from many small crystals and the ultrashort pulses are replaced by exposure times that are kept short enough to avoid significant crystal damage. The diffraction signal from each short exposure is so ‘sparse’ in recorded photons that the process of recording the crystal intensity is itself a reconstruction problem. Using the EMC algorithm, a successful reconstruction is demonstrated here in a sparsity regime where there are no Bragg peaks that conventionally would serve to determine the orientation of the crystal in each exposure. In this proof-of-principle experiment, a hen egg-white lysozyme (HEWL) crystal rotating about a single axis was illuminated by an X-ray beam from an X-ray generator to simulate the diffraction patterns of microcrystals from synchrotron radiation. Millions of these sparse frames, typically containing only ∼200 photons per frame, were recorded using a fast-framing detector. It is shown that reconstruction of three-dimensional diffraction intensity is possible using the EMC algorithm, even with these extremely sparse frames and without knowledge of the rotation angle. Further, the reconstructed intensity can be phased and refined to solve the protein structure using traditional crystallographic software. This suggests that synchrotron-based serial crystallography of micrometre-sized crystals can be practical with the aid of the EMC algorithm even in cases where the data are sparse. International Union of Crystallography 2016-01-01 /pmc/articles/PMC4704078/ /pubmed/26870380 http://dx.doi.org/10.1107/S2052252515018795 Text en © Jennifer L. Wierman et al. 2016 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Research Papers
Wierman, Jennifer L.
Lan, Ti-Yen
Tate, Mark W.
Philipp, Hugh T.
Elser, Veit
Gruner, Sol M.
Protein crystal structure from non-oriented, single-axis sparse X-ray data
title Protein crystal structure from non-oriented, single-axis sparse X-ray data
title_full Protein crystal structure from non-oriented, single-axis sparse X-ray data
title_fullStr Protein crystal structure from non-oriented, single-axis sparse X-ray data
title_full_unstemmed Protein crystal structure from non-oriented, single-axis sparse X-ray data
title_short Protein crystal structure from non-oriented, single-axis sparse X-ray data
title_sort protein crystal structure from non-oriented, single-axis sparse x-ray data
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4704078/
https://www.ncbi.nlm.nih.gov/pubmed/26870380
http://dx.doi.org/10.1107/S2052252515018795
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