New high-throughput endstation to accelerate the experimental optimization pipeline for synchrotron X-ray footprinting.
Bluesky
X-ray radiolysis
high throughput
hydroxyl radical footprinting
macromolecular dynamics
nucleic acids
protein structure
Journal
Journal of synchrotron radiation
ISSN: 1600-5775
Titre abrégé: J Synchrotron Radiat
Pays: United States
ID NLM: 9888878
Informations de publication
Date de publication:
01 Sep 2021
01 Sep 2021
Historique:
received:
01
02
2021
accepted:
11
05
2021
entrez:
3
9
2021
pubmed:
4
9
2021
medline:
24
9
2021
Statut:
ppublish
Résumé
Synchrotron X-ray footprinting (XF) is a growing structural biology technique that leverages radiation-induced chemical modifications via X-ray radiolysis of water to produce hydroxyl radicals that probe changes in macromolecular structure and dynamics in solution states of interest. The X-ray Footprinting of Biological Materials (XFP) beamline at the National Synchrotron Light Source II provides the structural biology community with access to instrumentation and expert support in the XF method, and is also a platform for development of new technological capabilities in this field. The design and implementation of a new high-throughput endstation device based around use of a 96-well PCR plate form factor and supporting diagnostic instrumentation for synchrotron XF is described. This development enables a pipeline for rapid comprehensive screening of the influence of sample chemistry on hydroxyl radical dose using a convenient fluorescent assay, illustrated here with a study of 26 organic compounds. The new high-throughput endstation device and sample evaluation pipeline now available at the XFP beamline provide the worldwide structural biology community with a robust resource for carrying out well optimized synchrotron XF studies of challenging biological systems with complex sample compositions.
Identifiants
pubmed: 34475281
pii: S1600577521005026
doi: 10.1107/S1600577521005026
pmc: PMC8415340
doi:
Substances chimiques
Proteins
0
Water
059QF0KO0R
Hydroxyl Radical
3352-57-6
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1321-1332Subventions
Organisme : U.S. Department of Energy, Office of Science
ID : DE-SC0012704
Organisme : National Science Foundation
ID : DBI-1228549
Organisme : NIBIB NIH HHS
ID : P30 EB009998
Pays : United States
Organisme : Air Force Research Laboratory
ID : FA8650-18-2-5402
Organisme : National Institutes of Health, National Institute of Biomedical Imaging and Bioengineering
ID : P30-EB-009998
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