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Modeling a unit cell: crystallographic refinement procedure using the biomolecular MD simulation platform Amber
A procedure has been developed for the refinement of crystallographic protein structures based on the biomolecular simulation program Amber. The procedure constructs a model representing a crystal unit cell, which generally contains multiple protein molecules and is fully hydrated with TIP3P water....
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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International Union of Crystallography
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8733891/ https://www.ncbi.nlm.nih.gov/pubmed/35059216 http://dx.doi.org/10.1107/S2052252521011891 |
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author | Mikhailovskii, Oleg Xue, Yi Skrynnikov, Nikolai R. |
author_facet | Mikhailovskii, Oleg Xue, Yi Skrynnikov, Nikolai R. |
author_sort | Mikhailovskii, Oleg |
collection | PubMed |
description | A procedure has been developed for the refinement of crystallographic protein structures based on the biomolecular simulation program Amber. The procedure constructs a model representing a crystal unit cell, which generally contains multiple protein molecules and is fully hydrated with TIP3P water. Periodic boundary conditions are applied to the cell in order to emulate the crystal lattice. The refinement is conducted in the form of a specially designed short molecular-dynamics run controlled by the Amber ff14SB force field and the maximum-likelihood potential that encodes the structure-factor-based restraints. The new Amber-based refinement procedure has been tested on a set of 84 protein structures. In most cases, the new procedure led to appreciably lower R (free) values compared with those reported in the original PDB depositions or obtained by means of the industry-standard phenix.refine program. In particular, the new method has the edge in refining low-accuracy scrambled models. It has also been successful in refining a number of molecular-replacement models, including one with an r.m.s.d. of 2.15 Å. In addition, Amber-refined structures consistently show superior MolProbity scores. The new approach offers a highly realistic representation of protein–protein interactions in the crystal, as well as of protein–water interactions. It also offers a realistic representation of protein crystal dynamics (akin to ensemble-refinement schemes). Importantly, the method fully utilizes the information from the available diffraction data, while relying on state-of-the-art molecular-dynamics modeling to assist with those elements of the structure that do not diffract well (for example mobile loops or side chains). Finally, it should be noted that the protocol employs no tunable parameters, and the calculations can be conducted in a matter of several hours on desktop computers equipped with graphical processing units or using a designated web service. |
format | Online Article Text |
id | pubmed-8733891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-87338912022-01-19 Modeling a unit cell: crystallographic refinement procedure using the biomolecular MD simulation platform Amber Mikhailovskii, Oleg Xue, Yi Skrynnikov, Nikolai R. IUCrJ Research Papers A procedure has been developed for the refinement of crystallographic protein structures based on the biomolecular simulation program Amber. The procedure constructs a model representing a crystal unit cell, which generally contains multiple protein molecules and is fully hydrated with TIP3P water. Periodic boundary conditions are applied to the cell in order to emulate the crystal lattice. The refinement is conducted in the form of a specially designed short molecular-dynamics run controlled by the Amber ff14SB force field and the maximum-likelihood potential that encodes the structure-factor-based restraints. The new Amber-based refinement procedure has been tested on a set of 84 protein structures. In most cases, the new procedure led to appreciably lower R (free) values compared with those reported in the original PDB depositions or obtained by means of the industry-standard phenix.refine program. In particular, the new method has the edge in refining low-accuracy scrambled models. It has also been successful in refining a number of molecular-replacement models, including one with an r.m.s.d. of 2.15 Å. In addition, Amber-refined structures consistently show superior MolProbity scores. The new approach offers a highly realistic representation of protein–protein interactions in the crystal, as well as of protein–water interactions. It also offers a realistic representation of protein crystal dynamics (akin to ensemble-refinement schemes). Importantly, the method fully utilizes the information from the available diffraction data, while relying on state-of-the-art molecular-dynamics modeling to assist with those elements of the structure that do not diffract well (for example mobile loops or side chains). Finally, it should be noted that the protocol employs no tunable parameters, and the calculations can be conducted in a matter of several hours on desktop computers equipped with graphical processing units or using a designated web service. International Union of Crystallography 2021-12-16 /pmc/articles/PMC8733891/ /pubmed/35059216 http://dx.doi.org/10.1107/S2052252521011891 Text en © Oleg Mikhailovskii et al. 2022 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Research Papers Mikhailovskii, Oleg Xue, Yi Skrynnikov, Nikolai R. Modeling a unit cell: crystallographic refinement procedure using the biomolecular MD simulation platform Amber |
title | Modeling a unit cell: crystallographic refinement procedure using the biomolecular MD simulation platform Amber
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title_full | Modeling a unit cell: crystallographic refinement procedure using the biomolecular MD simulation platform Amber
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title_fullStr | Modeling a unit cell: crystallographic refinement procedure using the biomolecular MD simulation platform Amber
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title_full_unstemmed | Modeling a unit cell: crystallographic refinement procedure using the biomolecular MD simulation platform Amber
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title_short | Modeling a unit cell: crystallographic refinement procedure using the biomolecular MD simulation platform Amber
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title_sort | modeling a unit cell: crystallographic refinement procedure using the biomolecular md simulation platform amber |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8733891/ https://www.ncbi.nlm.nih.gov/pubmed/35059216 http://dx.doi.org/10.1107/S2052252521011891 |
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