Literature DB >> 26391007

The influence of frame alignment with dose compensation on the quality of single particle reconstructions.

John M Spear1, Alex J Noble2, Qing Xie3, Duncan R Sousa4, Michael S Chapman3, Scott M Stagg5.   

Abstract

As direct electron detection devices in cryo-electron microscopy become ubiquitous, the field is now ripe for new developments in image analysis techniques that take advantage of their increased SNR coupled with their high-throughput frame collection abilities. In approaching atomic resolution of native-like biomolecules, the accurate extraction of structural locations and orientations of side-chains from frames depends not only on the electron dose that a sample receives but also on the ability to accurately estimate the CTF. Here we use a new 2.8Å resolution structure of a recombinant gene therapy virus, AAV-DJ with Arixtra, imaged on an FEI Titan Krios with a DE-20 direct electron detector to probe new metrics including relative side-chain density and ResLog analysis for optimizing the compensation of electron beam damage and to characterize the factors that are limiting the resolution of the reconstruction. The influence of dose compensation on the accuracy of CTF estimation and particle classifiability are also presented. We show that rigorous dose compensation allows for better particle classifiability and greater recovery of structural information from negatively charged, electron-sensitive side-chains, resulting in a more accurate macromolecular model.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Atomic resolution; Beam-induced motion; Cryo-electron microscopy; Direct electron detector; Dose compensation; Radiation damage

Mesh:

Substances:

Year:  2015        PMID: 26391007      PMCID: PMC4633374          DOI: 10.1016/j.jsb.2015.09.006

Source DB:  PubMed          Journal:  J Struct Biol        ISSN: 1047-8477            Impact factor:   2.867


  39 in total

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Authors:  S J Ludtke; P R Baldwin; W Chiu
Journal:  J Struct Biol       Date:  1999-12-01       Impact factor: 2.867

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Authors:  Joseph A Mindell; Nikolaus Grigorieff
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3.  ResLog plots as an empirical metric of the quality of cryo-EM reconstructions.

Authors:  Scott M Stagg; Alex J Noble; Michael Spilman; Michael S Chapman
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4.  Structure of the E. coli ribosome-EF-Tu complex at <3 Å resolution by Cs-corrected cryo-EM.

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Authors:  K Mitsuoka; T Hirai; K Murata; A Miyazawa; A Kidera; Y Kimura; Y Fujiyoshi
Journal:  J Mol Biol       Date:  1999-02-26       Impact factor: 5.469

6.  Creating an infrastructure for high-throughput high-resolution cryogenic electron microscopy.

Authors:  Donald C Shrum; Brent W Woodruff; Scott M Stagg
Journal:  J Struct Biol       Date:  2012-07-25       Impact factor: 2.867

7.  Exploration of parameters in cryo-EM leading to an improved density map of the E. coli ribosome.

Authors:  Jamie LeBarron; Robert A Grassucci; Tanvir R Shaikh; William T Baxter; Jayati Sengupta; Joachim Frank
Journal:  J Struct Biol       Date:  2008-06-18       Impact factor: 2.867

8.  Atomic-accuracy models from 4.5-Å cryo-electron microscopy data with density-guided iterative local refinement.

Authors:  Frank DiMaio; Yifan Song; Xueming Li; Matthias J Brunner; Chunfu Xu; Vincent Conticello; Edward Egelman; Thomas Marlovits; Yifan Cheng; David Baker
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3.  Structural Heterogeneity in Pre-40S Ribosomes.

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8.  Processing apoferritin with the Appion pipeline.

Authors:  Scott M Stagg; Joshua H Mendez
Journal:  J Struct Biol       Date:  2018-06-30       Impact factor: 2.867

9.  Atomic Resolution Structures of Human Bufaviruses Determined by Cryo-Electron Microscopy.

Authors:  Maria Ilyas; Mario Mietzsch; Shweta Kailasan; Elina Väisänen; Mengxiao Luo; Paul Chipman; J Kennon Smith; Justin Kurian; Duncan Sousa; Robert McKenna; Maria Söderlund-Venermo; Mavis Agbandje-McKenna
Journal:  Viruses       Date:  2018-01-04       Impact factor: 5.048

10.  Adeno-associated Virus 9 Structural Rearrangements Induced by Endosomal Trafficking pH and Glycan Attachment.

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