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Pi sampling: a methodical and flexible approach to initial macromolecular crystallization screening

The Pi sampling method is derived from the incomplete factorial approach to macromolecular crystallization screen design. The resulting ‘Pi screens’ have a modular distribution of a given set of up to 36 stock solutions. Maximally diverse conditions can be produced by taking into account the propert...

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Detalles Bibliográficos
Autores principales: Gorrec, Fabrice, Palmer, Colin M., Lebon, Guillaume, Warne, Tony
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3087625/
https://www.ncbi.nlm.nih.gov/pubmed/21543849
http://dx.doi.org/10.1107/S0907444911008754
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author Gorrec, Fabrice
Palmer, Colin M.
Lebon, Guillaume
Warne, Tony
author_facet Gorrec, Fabrice
Palmer, Colin M.
Lebon, Guillaume
Warne, Tony
author_sort Gorrec, Fabrice
collection PubMed
description The Pi sampling method is derived from the incomplete factorial approach to macromolecular crystallization screen design. The resulting ‘Pi screens’ have a modular distribution of a given set of up to 36 stock solutions. Maximally diverse conditions can be produced by taking into account the properties of the chemicals used in the formulation and the concentrations of the corresponding solutions. The Pi sampling method has been implemented in a web-based application that generates screen formulations and recipes. It is particularly adapted to screens consisting of 96 different conditions. The flexibility and efficiency of Pi sampling is demonstrated by the crystallization of soluble proteins and of an integral membrane-protein sample.
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spelling pubmed-30876252011-05-10 Pi sampling: a methodical and flexible approach to initial macromolecular crystallization screening Gorrec, Fabrice Palmer, Colin M. Lebon, Guillaume Warne, Tony Acta Crystallogr D Biol Crystallogr Research Papers The Pi sampling method is derived from the incomplete factorial approach to macromolecular crystallization screen design. The resulting ‘Pi screens’ have a modular distribution of a given set of up to 36 stock solutions. Maximally diverse conditions can be produced by taking into account the properties of the chemicals used in the formulation and the concentrations of the corresponding solutions. The Pi sampling method has been implemented in a web-based application that generates screen formulations and recipes. It is particularly adapted to screens consisting of 96 different conditions. The flexibility and efficiency of Pi sampling is demonstrated by the crystallization of soluble proteins and of an integral membrane-protein sample. International Union of Crystallography 2011-04-07 /pmc/articles/PMC3087625/ /pubmed/21543849 http://dx.doi.org/10.1107/S0907444911008754 Text en © Gorrec et al. 2011 http://creativecommons.org/licenses/by/2.0/uk/ 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.
spellingShingle Research Papers
Gorrec, Fabrice
Palmer, Colin M.
Lebon, Guillaume
Warne, Tony
Pi sampling: a methodical and flexible approach to initial macromolecular crystallization screening
title Pi sampling: a methodical and flexible approach to initial macromolecular crystallization screening
title_full Pi sampling: a methodical and flexible approach to initial macromolecular crystallization screening
title_fullStr Pi sampling: a methodical and flexible approach to initial macromolecular crystallization screening
title_full_unstemmed Pi sampling: a methodical and flexible approach to initial macromolecular crystallization screening
title_short Pi sampling: a methodical and flexible approach to initial macromolecular crystallization screening
title_sort pi sampling: a methodical and flexible approach to initial macromolecular crystallization screening
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3087625/
https://www.ncbi.nlm.nih.gov/pubmed/21543849
http://dx.doi.org/10.1107/S0907444911008754
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