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Guide for determination of protein structural ensembles by combining cryo‐EM data with metadynamics
Metadynamics electron microscopy metaInference (MEMMI) is an integrative structural biology method that enables a rapid and accurate characterization of protein structural dynamics at the atomic level and the error in the cryo‐EM experimental data, even in cases where conformations are separated by...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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John Wiley and Sons Inc.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315759/ https://www.ncbi.nlm.nih.gov/pubmed/36562694 http://dx.doi.org/10.1002/2211-5463.13542 |
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author | Brotzakis, Z. Faidon |
author_facet | Brotzakis, Z. Faidon |
author_sort | Brotzakis, Z. Faidon |
collection | PubMed |
description | Metadynamics electron microscopy metaInference (MEMMI) is an integrative structural biology method that enables a rapid and accurate characterization of protein structural dynamics at the atomic level and the error in the cryo‐EM experimental data, even in cases where conformations are separated by high energy barriers. It achieves this by incorporating (a) cryo‐electron microscopy electron density maps with (b) metadynamic‐enhanced‐sampling molecular dynamics. Here, I showcase the setup and analysis protocol of MEMMI, used to discover the atomistic structural ensemble and error in the cryo‐EM electron density map of the fuzzy coat of IAPP, a fibril implicated in type II diabetes. |
format | Online Article Text |
id | pubmed-10315759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103157592023-07-04 Guide for determination of protein structural ensembles by combining cryo‐EM data with metadynamics Brotzakis, Z. Faidon FEBS Open Bio Research Protocol Metadynamics electron microscopy metaInference (MEMMI) is an integrative structural biology method that enables a rapid and accurate characterization of protein structural dynamics at the atomic level and the error in the cryo‐EM experimental data, even in cases where conformations are separated by high energy barriers. It achieves this by incorporating (a) cryo‐electron microscopy electron density maps with (b) metadynamic‐enhanced‐sampling molecular dynamics. Here, I showcase the setup and analysis protocol of MEMMI, used to discover the atomistic structural ensemble and error in the cryo‐EM electron density map of the fuzzy coat of IAPP, a fibril implicated in type II diabetes. John Wiley and Sons Inc. 2023-01-09 /pmc/articles/PMC10315759/ /pubmed/36562694 http://dx.doi.org/10.1002/2211-5463.13542 Text en © 2022 The Author. FEBS Open Bio published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Protocol Brotzakis, Z. Faidon Guide for determination of protein structural ensembles by combining cryo‐EM data with metadynamics |
title | Guide for determination of protein structural ensembles by combining cryo‐EM data with metadynamics |
title_full | Guide for determination of protein structural ensembles by combining cryo‐EM data with metadynamics |
title_fullStr | Guide for determination of protein structural ensembles by combining cryo‐EM data with metadynamics |
title_full_unstemmed | Guide for determination of protein structural ensembles by combining cryo‐EM data with metadynamics |
title_short | Guide for determination of protein structural ensembles by combining cryo‐EM data with metadynamics |
title_sort | guide for determination of protein structural ensembles by combining cryo‐em data with metadynamics |
topic | Research Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315759/ https://www.ncbi.nlm.nih.gov/pubmed/36562694 http://dx.doi.org/10.1002/2211-5463.13542 |
work_keys_str_mv | AT brotzakiszfaidon guidefordeterminationofproteinstructuralensemblesbycombiningcryoemdatawithmetadynamics |