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Title: Likelihood-based molecular-replacement solution for a highly pathological crystal with tetartohedral twinning and sevenfold translational noncrystallographic symmetry

Journal Article · · Acta Crystallographica. Section D: Biological Crystallography
 [1];  [1];  [2];
  1. Institute of Bioorganic Chemistry, Polish Academy of Sciences, Noskowskiego 12/14, 61-704 Poznan (Poland)
  2. National Cancer Institute, Argonne National Laboratory, Argonne, IL 60439 (United States)

With the implementation of a molecular-replacement likelihood target that accounts for translational noncrystallographic symmetry, it became possible to solve the crystal structure of a protein with seven tetrameric assemblies arrayed translationally along the c axis. The new algorithm found 56 protein molecules in reduced symmetry (P1), which was used to resolve space-group ambiguity caused by severe twinning. Translational noncrystallographic symmetry (tNCS) is a pathology of protein crystals in which multiple copies of a molecule or assembly are found in similar orientations. Structure solution is problematic because this breaks the assumptions used in current likelihood-based methods. To cope with such cases, new likelihood approaches have been developed and implemented in Phaser to account for the statistical effects of tNCS in molecular replacement. Using these new approaches, it was possible to solve the crystal structure of a protein exhibiting an extreme form of this pathology with seven tetrameric assemblies arrayed along the c axis. To resolve space-group ambiguities caused by tetartohedral twinning, the structure was initially solved by placing 56 copies of the monomer in space group P1 and using the symmetry of the solution to define the true space group, C2. The resulting structure of Hyp-1, a pathogenesis-related class 10 (PR-10) protein from the medicinal herb St John’s wort, reveals the binding modes of the fluorescent probe 8-anilino-1-naphthalene sulfonate (ANS), providing insight into the function of the protein in binding or storing hydrophobic ligands.

OSTI ID:
22347780
Journal Information:
Acta Crystallographica. Section D: Biological Crystallography, Vol. 70, Issue Pt 2; Other Information: PMCID: PMC3940205; PMID: 24531481; PUBLISHER-ID: yt5061; OAI: oai:pubmedcentral.nih.gov:3940205; Copyright (c) Sliwiak et al. 2014; This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.; Country of input: International Atomic Energy Agency (IAEA); ISSN 0907-4449
Country of Publication:
Denmark
Language:
English

Cited By (8)

Experiences with applications of macromolecular tools in supramolecular crystallography journal January 2014
Characterizing pathological imperfections in macromolecular crystals: lattice disorders and modulations journal December 2019
ARCIMBOLDO on coiled coils journal March 2018
On the application of the expected log-likelihood gain to decision making in molecular replacement journal April 2018
Coping with strong translational noncrystallographic symmetry and extreme anisotropy in molecular replacement with Phaser : human Rab27a journal February 2019
Supercell refinement: a cautionary tale journal August 2019
Acknowledging Errors: Advanced Molecular Replacement with Phaser text January 2016
On the application of the expected log-likelihood gain to decision making in molecular replacement. text January 2018