IceBear: an intuitive and versatile web application for research-data tracking from crystallization experiment to PDB deposition.
ISPyB
IceBear
X-ray data collection
crystallization
metadata
research-data management
Journal
Acta crystallographica. Section D, Structural biology
ISSN: 2059-7983
Titre abrégé: Acta Crystallogr D Struct Biol
Pays: United States
ID NLM: 101676043
Informations de publication
Date de publication:
01 Feb 2021
01 Feb 2021
Historique:
received:
15
10
2020
accepted:
15
11
2020
entrez:
9
2
2021
pubmed:
10
2
2021
medline:
4
9
2021
Statut:
ppublish
Résumé
The web-based IceBear software is a versatile tool to monitor the results of crystallization experiments and is designed to facilitate supervisor and student communications. It also records and tracks all relevant information from crystallization setup to PDB deposition in protein crystallography projects. Fully automated data collection is now possible at several synchrotrons, which means that the number of samples tested at the synchrotron is currently increasing rapidly. Therefore, the protein crystallography research communities at the University of Oulu, Weizmann Institute of Science and Diamond Light Source have joined forces to automate the uploading of sample metadata to the synchrotron. In IceBear, each crystal selected for data collection is given a unique sample name and a crystal page is generated. Subsequently, the metadata required for data collection are uploaded directly to the ISPyB synchrotron database by a shipment module, and for each sample a link to the relevant ISPyB page is stored. IceBear allows notes to be made for each sample during cryocooling treatment and during data collection, as well as in later steps of the structure determination. Protocols are also available to aid the recycling of pins, pucks and dewars when the dewar returns from the synchrotron. The IceBear database is organized around projects, and project members can easily access the crystallization and diffraction metadata for each sample, as well as any additional information that has been provided via the notes. The crystal page for each sample connects the crystallization, diffraction and structural information by providing links to the IceBear drop-viewer page and to the ISPyB data-collection page, as well as to the structure deposited in the Protein Data Bank.
Identifiants
pubmed: 33559605
pii: S2059798320015223
doi: 10.1107/S2059798320015223
pmc: PMC7869904
doi:
Substances chimiques
Proteins
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
151-163Subventions
Organisme : Horizon 2020
ID : 731005
Organisme : Academy of Finland
ID : 328117
Organisme : Academy of Finland
ID : 287063
Organisme : Academy of Finland
ID : 294085
Organisme : Academy of Finland
ID : 297875
Organisme : Academy of Finland
ID : 141487
Organisme : Academy of Finland
ID : 293369
Organisme : Academy of Finland
ID : 289024
Organisme : Academy of Finland
ID : 319194
Informations de copyright
open access.
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