<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jain R</submitter><funding>NIBIB NIH HHS</funding><funding>U.S. Department of Energy, Office of Science</funding><funding>Air Force Research Laboratory</funding><funding>Case Western Reserve University</funding><funding>National Institutes of Health, National Institute of Biomedical Imaging and Bioengineering</funding><funding>Brookhaven National Laboratory</funding><funding>National Science Foundation</funding><pagination>1321-1332</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8415340</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(Pt 5)</volume><pubmed_abstract>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 develo</pubmed_abstract><journal>Journal of synchrotron radiation</journal><pubmed_title>New high-throughput endstation to accelerate the experimental optimization pipeline for synchrotron X-ray footprinting.</pubmed_title><pmcid>PMC8415340</pmcid><funding_grant_id>FA8650-18-2-5402</funding_grant_id><funding_grant_id>DBI-1228549</funding_grant_id><funding_grant_id>P30 EB009998</funding_grant_id><funding_grant_id>DE-SC0012704</funding_grant_id><funding_grant_id>P30-EB-009998</funding_grant_id><pubmed_authors>Jain R</pubmed_authors><pubmed_authors>Rakitin M</pubmed_authors><pubmed_authors>Abel D</pubmed_authors><pubmed_authors>Sullivan M</pubmed_authors><pubmed_authors>Chance MR</pubmed_authors><pubmed_authors>Farquhar ER</pubmed_authors><pubmed_authors>Lodowski DT</pubmed_authors></additional><is_claimable>false</is_claimable><name>New high-throughput endstation to accelerate the experimental optimization pipeline for synchrotron X-ray footprinting.</name><description>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 develo</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2026-06-02T21:53:32.882Z</modification><creation>2025-04-04T09:37:21.749Z</creation></dates><accession>S-EPMC8415340</accession><cross_references><pubmed>34475281</pubmed><doi>10.1107/S1600577521005026</doi><doi>10.1107/s1600577521005026</doi></cross_references></HashMap>