Cargando…
High-resolution Single Particle Analysis from Electron Cryo-microscopy Images Using SPHIRE
SPHIRE (SPARX for High-Resolution Electron Microscopy) is a novel open-source, user-friendly software suite for the semi-automated processing of single particle electron cryo-microscopy (cryo-EM) data. The protocol presented here describes in detail how to obtain a near-atomic resolution structure s...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MyJove Corporation
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607996/ https://www.ncbi.nlm.nih.gov/pubmed/28570515 http://dx.doi.org/10.3791/55448 |
_version_ | 1783265371684339712 |
---|---|
author | Moriya, Toshio Saur, Michael Stabrin, Markus Merino, Felipe Voicu, Horatiu Huang, Zhong Penczek, Pawel A. Raunser, Stefan Gatsogiannis, Christos |
author_facet | Moriya, Toshio Saur, Michael Stabrin, Markus Merino, Felipe Voicu, Horatiu Huang, Zhong Penczek, Pawel A. Raunser, Stefan Gatsogiannis, Christos |
author_sort | Moriya, Toshio |
collection | PubMed |
description | SPHIRE (SPARX for High-Resolution Electron Microscopy) is a novel open-source, user-friendly software suite for the semi-automated processing of single particle electron cryo-microscopy (cryo-EM) data. The protocol presented here describes in detail how to obtain a near-atomic resolution structure starting from cryo-EM micrograph movies by guiding users through all steps of the single particle structure determination pipeline. These steps are controlled from the new SPHIRE graphical user interface and require minimum user intervention. Using this protocol, a 3.5 Å structure of TcdA1, a Tc toxin complex from Photorhabdus luminescens, was derived from only 9500 single particles. This streamlined approach will help novice users without extensive processing experience and a priori structural information, to obtain noise-free and unbiased atomic models of their purified macromolecular complexes in their native state. |
format | Online Article Text |
id | pubmed-5607996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MyJove Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-56079962017-10-10 High-resolution Single Particle Analysis from Electron Cryo-microscopy Images Using SPHIRE Moriya, Toshio Saur, Michael Stabrin, Markus Merino, Felipe Voicu, Horatiu Huang, Zhong Penczek, Pawel A. Raunser, Stefan Gatsogiannis, Christos J Vis Exp Biochemistry SPHIRE (SPARX for High-Resolution Electron Microscopy) is a novel open-source, user-friendly software suite for the semi-automated processing of single particle electron cryo-microscopy (cryo-EM) data. The protocol presented here describes in detail how to obtain a near-atomic resolution structure starting from cryo-EM micrograph movies by guiding users through all steps of the single particle structure determination pipeline. These steps are controlled from the new SPHIRE graphical user interface and require minimum user intervention. Using this protocol, a 3.5 Å structure of TcdA1, a Tc toxin complex from Photorhabdus luminescens, was derived from only 9500 single particles. This streamlined approach will help novice users without extensive processing experience and a priori structural information, to obtain noise-free and unbiased atomic models of their purified macromolecular complexes in their native state. MyJove Corporation 2017-05-16 /pmc/articles/PMC5607996/ /pubmed/28570515 http://dx.doi.org/10.3791/55448 Text en Copyright © 2017, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Biochemistry Moriya, Toshio Saur, Michael Stabrin, Markus Merino, Felipe Voicu, Horatiu Huang, Zhong Penczek, Pawel A. Raunser, Stefan Gatsogiannis, Christos High-resolution Single Particle Analysis from Electron Cryo-microscopy Images Using SPHIRE |
title | High-resolution Single Particle Analysis from Electron Cryo-microscopy Images Using SPHIRE |
title_full | High-resolution Single Particle Analysis from Electron Cryo-microscopy Images Using SPHIRE |
title_fullStr | High-resolution Single Particle Analysis from Electron Cryo-microscopy Images Using SPHIRE |
title_full_unstemmed | High-resolution Single Particle Analysis from Electron Cryo-microscopy Images Using SPHIRE |
title_short | High-resolution Single Particle Analysis from Electron Cryo-microscopy Images Using SPHIRE |
title_sort | high-resolution single particle analysis from electron cryo-microscopy images using sphire |
topic | Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607996/ https://www.ncbi.nlm.nih.gov/pubmed/28570515 http://dx.doi.org/10.3791/55448 |
work_keys_str_mv | AT moriyatoshio highresolutionsingleparticleanalysisfromelectroncryomicroscopyimagesusingsphire AT saurmichael highresolutionsingleparticleanalysisfromelectroncryomicroscopyimagesusingsphire AT stabrinmarkus highresolutionsingleparticleanalysisfromelectroncryomicroscopyimagesusingsphire AT merinofelipe highresolutionsingleparticleanalysisfromelectroncryomicroscopyimagesusingsphire AT voicuhoratiu highresolutionsingleparticleanalysisfromelectroncryomicroscopyimagesusingsphire AT huangzhong highresolutionsingleparticleanalysisfromelectroncryomicroscopyimagesusingsphire AT penczekpawela highresolutionsingleparticleanalysisfromelectroncryomicroscopyimagesusingsphire AT raunserstefan highresolutionsingleparticleanalysisfromelectroncryomicroscopyimagesusingsphire AT gatsogiannischristos highresolutionsingleparticleanalysisfromelectroncryomicroscopyimagesusingsphire |