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FragMAX: the fragment-screening platform at the MAX IV Laboratory

Advances in synchrotron storage rings and beamline automation have pushed data-collection rates to thousands of data sets per week. With this increase in throughput, massive projects such as in-crystal fragment screening have become accessible to a larger number of research groups. The quality of su...

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Autores principales: Lima, Gustavo M. A., Talibov, Vladimir O., Jagudin, Elmir, Sele, Céleste, Nyblom, Maria, Knecht, Wolfgang, Logan, Derek T., Sjögren, Tove, Mueller, Uwe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397489/
https://www.ncbi.nlm.nih.gov/pubmed/32744259
http://dx.doi.org/10.1107/S205979832000889X
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author Lima, Gustavo M. A.
Talibov, Vladimir O.
Jagudin, Elmir
Sele, Céleste
Nyblom, Maria
Knecht, Wolfgang
Logan, Derek T.
Sjögren, Tove
Mueller, Uwe
author_facet Lima, Gustavo M. A.
Talibov, Vladimir O.
Jagudin, Elmir
Sele, Céleste
Nyblom, Maria
Knecht, Wolfgang
Logan, Derek T.
Sjögren, Tove
Mueller, Uwe
author_sort Lima, Gustavo M. A.
collection PubMed
description Advances in synchrotron storage rings and beamline automation have pushed data-collection rates to thousands of data sets per week. With this increase in throughput, massive projects such as in-crystal fragment screening have become accessible to a larger number of research groups. The quality of support offered at large-scale facilities allows medicinal chemistry-focused or biochemistry-focused groups to supplement their research with structural biology. Preparing the experiment, analysing multiple data sets and prospecting for interesting complexes of protein and fragments require, for both newcomers and experienced users, efficient management of the project and extensive computational power for data processing and structure refinement. Here, FragMAX, a new complete platform for fragment screening at the BioMAX beamline of the MAX IV Laboratory, is described. The ways in which users are assisted in X-ray-based fragment screenings and in which the fourth-generation storage ring available at the facility is best exploited are also described.
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spelling pubmed-73974892020-08-11 FragMAX: the fragment-screening platform at the MAX IV Laboratory Lima, Gustavo M. A. Talibov, Vladimir O. Jagudin, Elmir Sele, Céleste Nyblom, Maria Knecht, Wolfgang Logan, Derek T. Sjögren, Tove Mueller, Uwe Acta Crystallogr D Struct Biol Research Papers Advances in synchrotron storage rings and beamline automation have pushed data-collection rates to thousands of data sets per week. With this increase in throughput, massive projects such as in-crystal fragment screening have become accessible to a larger number of research groups. The quality of support offered at large-scale facilities allows medicinal chemistry-focused or biochemistry-focused groups to supplement their research with structural biology. Preparing the experiment, analysing multiple data sets and prospecting for interesting complexes of protein and fragments require, for both newcomers and experienced users, efficient management of the project and extensive computational power for data processing and structure refinement. Here, FragMAX, a new complete platform for fragment screening at the BioMAX beamline of the MAX IV Laboratory, is described. The ways in which users are assisted in X-ray-based fragment screenings and in which the fourth-generation storage ring available at the facility is best exploited are also described. International Union of Crystallography 2020-07-27 /pmc/articles/PMC7397489/ /pubmed/32744259 http://dx.doi.org/10.1107/S205979832000889X Text en © Lima et al. 2020 http://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.http://creativecommons.org/licenses/by/4.0/
spellingShingle Research Papers
Lima, Gustavo M. A.
Talibov, Vladimir O.
Jagudin, Elmir
Sele, Céleste
Nyblom, Maria
Knecht, Wolfgang
Logan, Derek T.
Sjögren, Tove
Mueller, Uwe
FragMAX: the fragment-screening platform at the MAX IV Laboratory
title FragMAX: the fragment-screening platform at the MAX IV Laboratory
title_full FragMAX: the fragment-screening platform at the MAX IV Laboratory
title_fullStr FragMAX: the fragment-screening platform at the MAX IV Laboratory
title_full_unstemmed FragMAX: the fragment-screening platform at the MAX IV Laboratory
title_short FragMAX: the fragment-screening platform at the MAX IV Laboratory
title_sort fragmax: the fragment-screening platform at the max iv laboratory
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397489/
https://www.ncbi.nlm.nih.gov/pubmed/32744259
http://dx.doi.org/10.1107/S205979832000889X
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