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Characterisation of molecular motions in cryo-EM single-particle data by multi-body refinement in RELION
Macromolecular complexes that exhibit continuous forms of structural flexibility pose a challenge for many existing tools in cryo-EM single-particle analysis. We describe a new tool, called multi-body refinement, which models flexible complexes as a user-defined number of rigid bodies that move inde...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6005684/ https://www.ncbi.nlm.nih.gov/pubmed/29856314 http://dx.doi.org/10.7554/eLife.36861 |
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author | Nakane, Takanori Kimanius, Dari Lindahl, Erik Scheres, Sjors HW |
author_facet | Nakane, Takanori Kimanius, Dari Lindahl, Erik Scheres, Sjors HW |
author_sort | Nakane, Takanori |
collection | PubMed |
description | Macromolecular complexes that exhibit continuous forms of structural flexibility pose a challenge for many existing tools in cryo-EM single-particle analysis. We describe a new tool, called multi-body refinement, which models flexible complexes as a user-defined number of rigid bodies that move independently from each other. Using separate focused refinements with iteratively improved partial signal subtraction, the new tool generates improved reconstructions for each of the defined bodies in a fully automated manner. Moreover, using principal component analysis on the relative orientations of the bodies over all particle images in the data set, we generate movies that describe the most important motions in the data. Our results on two test cases, a cytoplasmic ribosome from Plasmodium falciparum, and the spliceosomal B-complex from yeast, illustrate how multi-body refinement can be useful to gain unique insights into the structure and dynamics of large and flexible macromolecular complexes. |
format | Online Article Text |
id | pubmed-6005684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-60056842018-06-20 Characterisation of molecular motions in cryo-EM single-particle data by multi-body refinement in RELION Nakane, Takanori Kimanius, Dari Lindahl, Erik Scheres, Sjors HW eLife Structural Biology and Molecular Biophysics Macromolecular complexes that exhibit continuous forms of structural flexibility pose a challenge for many existing tools in cryo-EM single-particle analysis. We describe a new tool, called multi-body refinement, which models flexible complexes as a user-defined number of rigid bodies that move independently from each other. Using separate focused refinements with iteratively improved partial signal subtraction, the new tool generates improved reconstructions for each of the defined bodies in a fully automated manner. Moreover, using principal component analysis on the relative orientations of the bodies over all particle images in the data set, we generate movies that describe the most important motions in the data. Our results on two test cases, a cytoplasmic ribosome from Plasmodium falciparum, and the spliceosomal B-complex from yeast, illustrate how multi-body refinement can be useful to gain unique insights into the structure and dynamics of large and flexible macromolecular complexes. eLife Sciences Publications, Ltd 2018-06-01 /pmc/articles/PMC6005684/ /pubmed/29856314 http://dx.doi.org/10.7554/eLife.36861 Text en © 2018, Nakane et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Structural Biology and Molecular Biophysics Nakane, Takanori Kimanius, Dari Lindahl, Erik Scheres, Sjors HW Characterisation of molecular motions in cryo-EM single-particle data by multi-body refinement in RELION |
title | Characterisation of molecular motions in cryo-EM single-particle data by multi-body refinement in RELION |
title_full | Characterisation of molecular motions in cryo-EM single-particle data by multi-body refinement in RELION |
title_fullStr | Characterisation of molecular motions in cryo-EM single-particle data by multi-body refinement in RELION |
title_full_unstemmed | Characterisation of molecular motions in cryo-EM single-particle data by multi-body refinement in RELION |
title_short | Characterisation of molecular motions in cryo-EM single-particle data by multi-body refinement in RELION |
title_sort | characterisation of molecular motions in cryo-em single-particle data by multi-body refinement in relion |
topic | Structural Biology and Molecular Biophysics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6005684/ https://www.ncbi.nlm.nih.gov/pubmed/29856314 http://dx.doi.org/10.7554/eLife.36861 |
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