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Coping with strong translational noncrystallographic symmetry and extreme anisotropy in molecular replacement with Phaser: human Rab27a

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Title: Coping with strong translational noncrystallographic symmetry and extreme anisotropy in molecular replacement with Phaser: human Rab27a
Authors: Jamshidiha, M
Pérez-Dorado, I
Murray, JW
Tate, EW
Cota, E
Read, RJ
Item Type: Journal Article
Abstract: Data pathologies caused by effects such as diffraction anisotropy and translational noncrystallographic symmetry (tNCS) can dramatically complicate the solution of the crystal structures of macromolecules. Such problems were encountered in determining the structure of a mutant form of Rab27a, a member of the Rab GTPases. Mutant Rab27a constructs that crystallize in the free form were designed for use in the discovery of drugs to reduce primary tumour invasiveness and metastasis. One construct, hRab27a<jats:sup>Mut</jats:sup>, crystallized within 24 h and diffracted to 2.82 Å resolution, with a unit cell possessing room for a large number of protein copies. Initial efforts to solve the structure using molecular replacement by <jats:italic>Phaser</jats:italic> were not successful. Analysis of the data set revealed that the crystals suffered from both extreme anisotropy and strong tNCS. As a result, large numbers of reflections had estimated standard deviations that were much larger than their measured intensities and their expected intensities, revealing problems with the use of such data at the time in <jats:italic>Phaser</jats:italic>. By eliminating extremely weak reflections with the largest combined effects of anisotropy and tNCS, these problems could be avoided, allowing a molecular-replacement solution to be found. The lessons that were learned in solving this structure have guided improvements in the numerical analysis used in <jats:italic>Phaser</jats:italic>, particularly in identifying diffraction measurements that convey very little information content. The calculation of information content could also be applied as an alternative to ellipsoidal truncation. The post-mortem analysis also revealed an oversight in accounting for measurement errors in the fast rotation function. While the crystal of mutant Rab27a is not amenable to drug screening, the structure can guide new modifications to obtain more suitable crystal forms.
Issue Date: 1-Mar-2019
Date of Acceptance: 17-Dec-2018
URI: http://hdl.handle.net/10044/1/69634
DOI: https://dx.doi.org/10.1107/s2059798318017825
ISSN: 2059-7983
Publisher: International Union of Crystallography (IUCr)
Start Page: 342
End Page: 353
Journal / Book Title: Acta Crystallographica Section D Structural Biology
Volume: 75
Issue: 3
Copyright Statement: © 2019 The Author(s). This is an open access article licensed under the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0/).
Sponsor/Funder: Cancer Research UK
Cancer Research UK
Funder's Grant Number: 20781
C29637/A27311
Keywords: Science & Technology
Life Sciences & Biomedicine
Physical Sciences
Biochemical Research Methods
Biochemistry & Molecular Biology
Biophysics
Crystallography
molecular replacement
Phaser
anisotropy
translational noncrystallography symmetry
Rab27a
information content
STRUCTURAL BASIS
EFFECTORS
CRYSTAL
RECRUITMENT
INVOLVEMENT
REFINEMENT
EXPRESSION
SECRETION
COMPLEXES
PROTEINS
Publication Status: Published
Article Number: di5025
Online Publication Date: 2019-02-28
Appears in Collections:Chemistry
Biological and Biophysical Chemistry
Faculty of Natural Sciences