A round-robin approach provides a detailed assessment of biomolecular small-angle scattering data reproducibility and yields consensus curves for benchmarking

Trewhella, J.; Vachette, P.; Bierma, J.; Blanchet, C.; Brookes, E.; Chakravarthy, S.; Chatzimagas, L.; Cleveland, T.E.; Cowieson, N.; Crossett, B.; Duff, A.P.; Franke, D.; Gabel, F.; Gillilan, R.E.; Graewert, M.; Grishaev, A.; Guss, J.M.; Hammel, M.; Hopkins, J.; Huang, Q.; Hub, J.S.; Hura, G.L.; Irving, T.C.; Jeffries, C.M.; Jeong, C.; Kirby, N.; Krueger, S.; Martel, A.; Matsui, T.; Li, N.; Pérez, J.; Porcar, L.; Prangé, T.; Rajkovic, I.; Rocco, M.; Rosenberg, D.J.; Ryan, T.M.; Seifert, S.; Sekiguchi, H.; Svergun, D.; Teixeira, S.; Thureau, A.; Weiss, T.M.; Whitten, A.E.; Wood, K.; Zuo, X.

doi:10.1107/S2059798322009184

Acta Crystallographica Section D
Acta Crystallographica
Section D STRUCTURAL BIOLOGY

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Figure 9
Data for (top to bottom traces) RNaseA, lysozyme, xylanase, urate oxidase and xylose isomerase from SEC–WAXS (black symbols, measured on the P12 BioSAXS beamline at EMBL, no lysozyme data) and batch WAXS (red symbols, measured on the 12-ID-B beamline at the APS, no urate oxidase data). The plot is log–log, with every second data point skipped for the sake of clarity and starting at q = 0.1 Å⁻¹ to better highlight the data beyond q = 1 Å⁻¹. Full log–log and log linear plots are given in Supplementary Fig. S12. Error bars are standard errors based on propagated counting statistics.

STRUCTURAL
BIOLOGY

ISSN: 2059-7983

Volume 78| Part 11| November 2022| Pages 1315-1336

https://doi.org/10.1107/S2059798322009184

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