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Structure, assembly and dynamics of macromolecular complexes by single particle cryo-electron microscopy
BACKGROUND: Proteins in their majority act rarely as single entities. Multisubunit macromolecular complexes are the actors in most of the cellular processes. These nanomachines are hold together by weak protein-protein interactions and undergo functionally important conformational changes. TFIID is...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4028798/ https://www.ncbi.nlm.nih.gov/pubmed/24565374 http://dx.doi.org/10.1186/1477-3155-11-S1-S4 |
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author | Durand, Alexandre Papai, Gabor Schultz, Patrick |
author_facet | Durand, Alexandre Papai, Gabor Schultz, Patrick |
author_sort | Durand, Alexandre |
collection | PubMed |
description | BACKGROUND: Proteins in their majority act rarely as single entities. Multisubunit macromolecular complexes are the actors in most of the cellular processes. These nanomachines are hold together by weak protein-protein interactions and undergo functionally important conformational changes. TFIID is such a multiprotein complex acting in eukaryotic transcription initiation. This complex is first to be recruited to the promoter of the genes and triggers the formation of the transcription preinitiation complex involving RNA polymerase II which leads to gene transcription. The exact role of TFIID in this process is not yet understood. METHODS: Last generation electron microscopes, improved data collection and new image analysis tools made it possible to obtain structural information of biological molecules at atomic resolution. Cryo-electron microscopy of vitrified samples visualizes proteins in a fully hydrated, close to native state. Molecular images are recorded at liquid nitrogen temperature in low electron dose conditions to reduce radiation damage. Digital image analysis of these noisy images aims at improving the signal-to-noise ratio, at separating distinct molecular views and at reconstructing a three-dimensional model of the biological particle. RESULTS: Using these methods we showed the early events of an activated transcription initiation process. We explored the interaction of the TFIID coactivator with the yeast Rap1 activator, the transcription factor TFIIA and the promoter DNA. We demonstrated that TFIID serves as an assembly platform for transient protein-protein interactions, which are essential for transcription initiation. CONCLUSIONS: Recent developments in electron microscopy have provided new insights into the structural organization and the dynamic reorganization of large macromolecular complexes. Examples of near-atomic resolutions exist but the molecular flexibility of macromolecular complexes remains the limiting factor in most case. Electron microscopy has the potential to provide both structural and dynamic information of biological assemblies in order to understand the molecular mechanisms of their functions. |
format | Online Article Text |
id | pubmed-4028798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40287982014-06-17 Structure, assembly and dynamics of macromolecular complexes by single particle cryo-electron microscopy Durand, Alexandre Papai, Gabor Schultz, Patrick J Nanobiotechnology Tutorial BACKGROUND: Proteins in their majority act rarely as single entities. Multisubunit macromolecular complexes are the actors in most of the cellular processes. These nanomachines are hold together by weak protein-protein interactions and undergo functionally important conformational changes. TFIID is such a multiprotein complex acting in eukaryotic transcription initiation. This complex is first to be recruited to the promoter of the genes and triggers the formation of the transcription preinitiation complex involving RNA polymerase II which leads to gene transcription. The exact role of TFIID in this process is not yet understood. METHODS: Last generation electron microscopes, improved data collection and new image analysis tools made it possible to obtain structural information of biological molecules at atomic resolution. Cryo-electron microscopy of vitrified samples visualizes proteins in a fully hydrated, close to native state. Molecular images are recorded at liquid nitrogen temperature in low electron dose conditions to reduce radiation damage. Digital image analysis of these noisy images aims at improving the signal-to-noise ratio, at separating distinct molecular views and at reconstructing a three-dimensional model of the biological particle. RESULTS: Using these methods we showed the early events of an activated transcription initiation process. We explored the interaction of the TFIID coactivator with the yeast Rap1 activator, the transcription factor TFIIA and the promoter DNA. We demonstrated that TFIID serves as an assembly platform for transient protein-protein interactions, which are essential for transcription initiation. CONCLUSIONS: Recent developments in electron microscopy have provided new insights into the structural organization and the dynamic reorganization of large macromolecular complexes. Examples of near-atomic resolutions exist but the molecular flexibility of macromolecular complexes remains the limiting factor in most case. Electron microscopy has the potential to provide both structural and dynamic information of biological assemblies in order to understand the molecular mechanisms of their functions. BioMed Central 2013-12-10 /pmc/articles/PMC4028798/ /pubmed/24565374 http://dx.doi.org/10.1186/1477-3155-11-S1-S4 Text en Copyright © 2013 Durand et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Tutorial Durand, Alexandre Papai, Gabor Schultz, Patrick Structure, assembly and dynamics of macromolecular complexes by single particle cryo-electron microscopy |
title | Structure, assembly and dynamics of macromolecular complexes by single particle cryo-electron microscopy |
title_full | Structure, assembly and dynamics of macromolecular complexes by single particle cryo-electron microscopy |
title_fullStr | Structure, assembly and dynamics of macromolecular complexes by single particle cryo-electron microscopy |
title_full_unstemmed | Structure, assembly and dynamics of macromolecular complexes by single particle cryo-electron microscopy |
title_short | Structure, assembly and dynamics of macromolecular complexes by single particle cryo-electron microscopy |
title_sort | structure, assembly and dynamics of macromolecular complexes by single particle cryo-electron microscopy |
topic | Tutorial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4028798/ https://www.ncbi.nlm.nih.gov/pubmed/24565374 http://dx.doi.org/10.1186/1477-3155-11-S1-S4 |
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