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9ER1

53fs pulse duration 100uJ pulse energy thaumatin

Summary for 9ER1
Entry DOI10.2210/pdb9er1/pdb
DescriptorThaumatin I, L(+)-TARTARIC ACID (3 entities in total)
Functional Keywordsradiation damage, xfel, pulse duration and intensity, disulphides, plant protein
Biological sourceThaumatococcus daniellii
Total number of polymer chains1
Total formula weight22378.13
Authors
Owen, R.L.,Hough, M.A.,Worrall, J.,Williams, L. (deposition date: 2024-03-22, release date: 2025-04-02, Last modification date: 2025-05-14)
Primary citationWilliams, L.J.,Thompson, A.J.,Dijkstal, P.,Appleby, M.,Assmann, G.,Dworkowski, F.S.N.,Hiller, N.,Huang, C.Y.,Mason, T.,Perrett, S.,Prat, E.,Voulot, D.,Pedrini, B.,Beale, J.H.,Hough, M.A.,Worrall, J.A.R.,Owen, R.L.
Damage before destruction? X-ray-induced changes in single-pulse serial femtosecond crystallography.
Iucrj, 12:358-371, 2025
Cited by
PubMed Abstract: Serial femtosecond crystallography (SFX) exploits extremely brief X-ray free-electron laser pulses to obtain diffraction data before destruction of the crystal. However, during the pulse X-ray-induced site-specific radiation damage can occur, leading to electronic state and/or structural changes. Here, we present a systematic exploration of the effect of single-pulse duration and energy (and consequently different dose rates) on site-specific radiation damage under typical SFX room-temperature experimental conditions. For the first time in SFX we directly measured the photon pulse duration, varying from less than 10 fs to more than 50 fs, and used three pulse energies to probe in-pulse damage in two radiation-sensitive proteins: the iron-heme peroxidase DtpAa and the disulfide-rich thaumatin. While difference-map features arising from radiation damage are observed, they do not lead to significant change in refined atomic coordinates or key bond lengths. Our work thus provides experimental verification that average atomic coordinates are not significantly perturbed by radiation damage in typical SFX experiments.
PubMed: 40227256
DOI: 10.1107/S2052252525002660
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.43 Å)
Structure validation

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