A flexible framework for multi-particle refinement in cryo-electron tomography

被引:38
作者
Burt, Alister [1 ]
Gaifas, Lorenzo [1 ]
Dendooven, Tom [2 ]
Gutsche, Irina [1 ]
机构
[1] Univ Grenoble Alpes, CNRS, CEA, Inst Biol Struct,IBS, Grenoble, France
[2] MRC Lab Mol Biol, Cambridge, England
基金
欧洲研究理事会;
关键词
CRYO-EM; RESOLUTION; DYNAMO;
D O I
10.1371/journal.pbio.3001319
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cryo-electron tomography (cryo-ET) and subtomogram averaging (STA) are increasingly used for macromolecular structure determination in situ. Here, we introduce a set of computational tools and resources designed to enable flexible approaches to STA through increased automation and simplified metadata handling. We create a bidirectional interface between the Dynamo software package and the Warp-Relion-M pipeline, providing a framework for ab initio and geometrical approaches to multiparticle refinement in M. We illustrate the power of working within this framework by applying it to EMPIAR-10164, a publicly available dataset containing immature HIV-1 virus-like particles (VLPs), and a challenging in situ dataset containing chemosensory arrays in bacterial minicells. Additionally, we provide a comprehensive, step-by-step guide to obtaining a 3.4-angstrom reconstruction from EMPIAR-10164. The guide is hosted on , a collaborative online platform we establish for sharing knowledge about cryo-ET.
引用
收藏
页数:16
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