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research article

A maximum likelihood approach to two-dimensional crystals

Zeng, Xiangyan
•
Stahlberg, Henning  orcid-logo
•
Grigorieff, Nikolaus
December 1, 2007
Journal of Structural Biology (JSB)

Maximum likelihood (ML) processing of transmission electron microscopy images of protein particles can produce reconstructions of superior resolution due to a reduced reference bias. We have investigated a ML processing approach to images centered on the unit cells of two-dimensional (2D) crystal images. The implemented software makes use of the predictive lattice node tracking in the MRC software, which is used to window particle stacks. These are then noise-whitened and subjected to ML processing. Resulting NIL maps are translated into amplitudes and phases for further processing within the 2dx software package. Compared with ML processing for randomly oriented single particles, the required computational costs are greatly reduced as the 2D crystals restrict the parameter search space. The software was applied to images of negatively stained or frozen hydrated 2D crystals of different crystal order. We find that the ML algorithm is not free from reference bias, even though its sensitivity to noise correlation is lower than for pure cross-correlation alignment. Compared with crystallographic processing, the newly developed software yields better resolution for 2D crystal images of lower crystal quality, and it performs equally well for well-ordered crystal images. (c) 2007 Elsevier Inc. All rights reserved.

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Type
research article
DOI
10.1016/j.jsb.2007.09.013
Author(s)
Zeng, Xiangyan
Stahlberg, Henning  orcid-logo
Grigorieff, Nikolaus
Date Issued

2007-12-01

Publisher

Elsevier

Published in
Journal of Structural Biology (JSB)
Volume

160

Issue

3

Start page

362

End page

374

Editorial or Peer reviewed

REVIEWED

Written at

OTHER

EPFL units
LBEM  
Available on Infoscience
February 13, 2020
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/165403
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