查看完整 summary.json 原文
{
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"title": "Probing the statistics of sequence-dependent DNA conformations in solution using SAXS.",
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"title": "Probing the statistics of sequence-dependent DNA conformations in solution using SAXS.",
"author_list": "Koning HJ, Pullakhandam A, Whitten AE, Bond CS, Peyrard M",
"journal": "Acta Crystallogr D Struct Biol",
"doi": "10.1107/S2059798325011556",
"pmid": "41553140",
"published_date": "2026 Feb 1"
},
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"released_date": "2025-08-12"
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"city": "Melbourne",
"country": "Australia",
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"name": "GAGE6 60bp dsDNA oligonucleotide",
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"deuteration": null,
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{
"short_name": null,
"address": null,
"full_name": "The University of Western Australia",
"webpage": null
}
],
"contributor_name": "Heidar",
"contributor_surname": "Koning",
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}
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"description": "Data was collected at the SAXS/WAXS beam line at the Australian Synchrotron (Melbourne, Australia) using a Pilatus3 S 2M detector at a sample-detector distance of 2.68 m and at a wavelength of λ = 0.107812 nm (I(s) vs s, where s = 4πsinθ/λ, and 2θ is the scattering angle). In-line size-exclusion chromatography (SEC) SAS was employed. The SEC parameters were as follows: A 50 μl sample at 2.587 mg/ml was injected onto a GE Superdex 200 5/150 column at 25°C using 150 mM KCl, 20 mM HEPES (pH 7.4), 5 mM MgCl2, 1 mM DTT, 5% glycerol buffer. 400 successive 1 second frames were collected. The data were normalized to the intensity of the transmitted beam and radially averaged; the scattering of the solvent-blank was subtracted. 2sigma errors from the Australian Synchrotron's SAXS/WAXS beamline have been divided by 2 to be compatible with expectations from the ATSAS package\r\n\r\nThis is the 60 bp GAGE6 oligo from Lee et al (2015); Wang et al (2022) which reportedly binds SFPQ. SAXS analysis indicates some degree of curvature which is likely due to the presence of multiple AT repeat regions in the sequence.",
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"symmetry": null,
"last_modified": "2026-02-23T09:45:35.560463+01:00",
"bragg_peak": []
}查看完整 manifest.json 原文
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