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Using cryo-electron microscopy maps for X-ray structure determination
X-ray crystallography and cryo-electron microscopy (cryo-EM) are complementary techniques for structure determination. Crystallography usually reveals more detailed information, while cryo-EM is an extremely useful technique for studying large-sized macromolecules. As the gap between the resolution...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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International Union of Crystallography
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038958/ https://www.ncbi.nlm.nih.gov/pubmed/30002839 http://dx.doi.org/10.1107/S2052252518005857 |
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author | Zeng, Lingxiao Ding, Wei Hao, Quan |
author_facet | Zeng, Lingxiao Ding, Wei Hao, Quan |
author_sort | Zeng, Lingxiao |
collection | PubMed |
description | X-ray crystallography and cryo-electron microscopy (cryo-EM) are complementary techniques for structure determination. Crystallography usually reveals more detailed information, while cryo-EM is an extremely useful technique for studying large-sized macromolecules. As the gap between the resolution of crystallography and cryo-EM data narrows, the cryo-EM map of a macromolecule could serve as an initial model to solve the phase problem of crystal diffraction for high-resolution structure determination. FSEARCH is a procedure to utilize the low-resolution molecular shape for crystallographic phasing. The IPCAS (Iterative Protein Crystal structure Automatic Solution) pipeline is an automatic direct-methods-aided dual-space iterative phasing and model-building procedure. When only an electron-density map is available as the starting point, IPCAS is capable of generating a completed model from the phases of the input map automatically, without the requirement of an initial model. In this study, a hybrid method integrating X-ray crystallography with cryo-EM to help with structure determination is presented. With a cryo-EM map as the starting point, the workflow of the method involves three steps. (1) Cryo-EM map replacement: FSEARCH is utilized to find the correct translation and orientation of the cryo-EM map in the crystallographic unit cell and generates the initial low-resolution map. (2) Phase extension: the phases calculated from the correctly placed cryo-EM map are extended to high-resolution X-ray data by non-crystallographic symmetry averaging with phenix.resolve. (3) Model building: IPCAS is used to generate an initial model using the phase-extended map and perform model completion by iteration. Four cases (the lowest cryo-EM map resolution being 6.9 Å) have been tested for the general applicability of the hybrid method, and almost complete models have been generated for all test cases with reasonable R (work)/R (free). The hybrid method therefore provides an automated tool for X-ray structure determination using a cryo-EM map as the starting point. |
format | Online Article Text |
id | pubmed-6038958 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-60389582018-07-12 Using cryo-electron microscopy maps for X-ray structure determination Zeng, Lingxiao Ding, Wei Hao, Quan IUCrJ Research Papers X-ray crystallography and cryo-electron microscopy (cryo-EM) are complementary techniques for structure determination. Crystallography usually reveals more detailed information, while cryo-EM is an extremely useful technique for studying large-sized macromolecules. As the gap between the resolution of crystallography and cryo-EM data narrows, the cryo-EM map of a macromolecule could serve as an initial model to solve the phase problem of crystal diffraction for high-resolution structure determination. FSEARCH is a procedure to utilize the low-resolution molecular shape for crystallographic phasing. The IPCAS (Iterative Protein Crystal structure Automatic Solution) pipeline is an automatic direct-methods-aided dual-space iterative phasing and model-building procedure. When only an electron-density map is available as the starting point, IPCAS is capable of generating a completed model from the phases of the input map automatically, without the requirement of an initial model. In this study, a hybrid method integrating X-ray crystallography with cryo-EM to help with structure determination is presented. With a cryo-EM map as the starting point, the workflow of the method involves three steps. (1) Cryo-EM map replacement: FSEARCH is utilized to find the correct translation and orientation of the cryo-EM map in the crystallographic unit cell and generates the initial low-resolution map. (2) Phase extension: the phases calculated from the correctly placed cryo-EM map are extended to high-resolution X-ray data by non-crystallographic symmetry averaging with phenix.resolve. (3) Model building: IPCAS is used to generate an initial model using the phase-extended map and perform model completion by iteration. Four cases (the lowest cryo-EM map resolution being 6.9 Å) have been tested for the general applicability of the hybrid method, and almost complete models have been generated for all test cases with reasonable R (work)/R (free). The hybrid method therefore provides an automated tool for X-ray structure determination using a cryo-EM map as the starting point. International Union of Crystallography 2018-05-11 /pmc/articles/PMC6038958/ /pubmed/30002839 http://dx.doi.org/10.1107/S2052252518005857 Text en © Zeng, Ding and Hao 2018 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.http://creativecommons.org/licenses/by/2.0/uk/ |
spellingShingle | Research Papers Zeng, Lingxiao Ding, Wei Hao, Quan Using cryo-electron microscopy maps for X-ray structure determination |
title | Using cryo-electron microscopy maps for X-ray structure determination |
title_full | Using cryo-electron microscopy maps for X-ray structure determination |
title_fullStr | Using cryo-electron microscopy maps for X-ray structure determination |
title_full_unstemmed | Using cryo-electron microscopy maps for X-ray structure determination |
title_short | Using cryo-electron microscopy maps for X-ray structure determination |
title_sort | using cryo-electron microscopy maps for x-ray structure determination |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038958/ https://www.ncbi.nlm.nih.gov/pubmed/30002839 http://dx.doi.org/10.1107/S2052252518005857 |
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