Literature DB >> 26592473

An approach to improve the resolution of helical filaments with a large axial rise and flexible subunits.

Shixin Yang1, John L Woodhead1, Fa-Qing Zhao1, Guidenn Sulbarán1, Roger Craig2.   

Abstract

Single particle analysis is widely used for three-dimensional reconstruction of helical filaments. Near-atomic resolution has been obtained for several well-ordered filaments. However, it is still a challenge to achieve high resolution for filaments with flexible subunits and a large axial rise per subunit relative to pixel size. Here, we describe an approach that improves the resolution in such cases. In filaments with a large axial rise, many segments must be shifted a long distance along the filament axis to match with a reference projection, potentially causing loss of alignment accuracy and hence resolution. In our study of myosin filaments, we overcame this problem by pre-determining the axial positions of myosin head crowns within segments to decrease the alignment error. In addition, homogeneous, well-ordered segments were selected from the raw data set by checking the assigned azimuthal rotation angle of segments in each filament against those expected for perfect helical symmetry. These procedures improved the resolution of the filament reconstruction from 30 Å to 13 Å. This approach could be useful in other helical filaments with a large axial rise and/or flexible subunits.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  3D reconstruction; Cryo-EM; Muscle contraction; Single particle analysis; Thick filament

Mesh:

Substances:

Year:  2015        PMID: 26592473      PMCID: PMC4696882          DOI: 10.1016/j.jsb.2015.11.007

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


  38 in total

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6.  Reconstruction of helical filaments and tubes.

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7.  Head-head interaction characterizes the relaxed state of Limulus muscle myosin filaments.

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Authors:  Maria E Zoghbi; John L Woodhead; Richard L Moss; Roger Craig
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9.  RELION: implementation of a Bayesian approach to cryo-EM structure determination.

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  11 in total

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Journal:  Appl Microsc       Date:  2017

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5.  Structure of myosin filaments from relaxed Lethocerus flight muscle by cryo-EM at 6 Å resolution.

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7.  CryoEM structure of Drosophila flight muscle thick filaments at 7 Å resolution.

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8.  Cryo-EM structure of the inhibited (10S) form of myosin II.

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Review 9.  Direct Visualization of Actin Filaments and Actin-Binding Proteins in Neuronal Cells.

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10.  The central role of the tail in switching off 10S myosin II activity.

Authors:  Shixin Yang; Kyoung Hwan Lee; John L Woodhead; Osamu Sato; Mitsuo Ikebe; Roger Craig
Journal:  J Gen Physiol       Date:  2019-08-06       Impact factor: 4.086

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