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Sabzian-Molaei, Fatemeh
Publications (3 of 3) Show all publications
Sabzian-Molaei, F., Orädd, F., Magkakis, K. & Andersson, M. (2026). A light-triggered time-resolved x-ray solution scattering (tr-xss) workflow with application to protein conformational dynamics. FEBS Open Bio
Open this publication in new window or tab >>A light-triggered time-resolved x-ray solution scattering (tr-xss) workflow with application to protein conformational dynamics
2026 (English)In: FEBS Open Bio, E-ISSN 2211-5463Article in journal (Refereed) Epub ahead of print
Abstract [en]

Time-resolved X-ray solution scattering (TR-XSS) is a synchrotron-based methodology that enables real-time structural characterization under near-native conditions to provide insight into dynamic and transient structural changes inaccessible to static high-resolution methods such as cryo-electron microscopy (cryo-EM) or X-ray crystallography. Here, we present a workflow for light-triggered TR-XSS experiments that spans data collection, data processing, kinetic analysis, and structural refinement, with accompanying Python scripts. A calcium-transporting P-type ATPase membrane protein (LMCA1) is used as an illustrative example, but the protocol is broadly applicable to diverse protein systems. This workflow offers a practical framework for collecting TR-XSS synchrotron data and subsequent data analysis and interpretation.

Place, publisher, year, edition, pages
John Wiley & Sons, 2026
Keywords
kinetic modeling, protein conformational dynamics, structural refinement, time-resolved X-ray solution scattering (TR-XSS)
National Category
Biochemistry Molecular Biology
Identifiers
urn:nbn:se:umu:diva-250064 (URN)10.1002/2211-5463.70200 (DOI)41669764 (PubMedID)2-s2.0-105029833005 (Scopus ID)
Funder
EU, Horizon 2020, 101081419Swedish Research Council, 2024-04385The Kempe Foundations, JCSMK 24-543
Available from: 2026-02-26 Created: 2026-02-26 Last updated: 2026-02-26
Sabzian-Molaei, F., Plivelic, T. S. & Andersson, M. (2026). Assessing protein-specific radiation damage in time-resolved X-ray solution-scattering experiments at high-brilliance synchrotrons using fast detector readout. Acta Crystallographica Section D: Structural Biology , 82(7), 715-726
Open this publication in new window or tab >>Assessing protein-specific radiation damage in time-resolved X-ray solution-scattering experiments at high-brilliance synchrotrons using fast detector readout
2026 (English)In: Acta Crystallographica Section D: Structural Biology , E-ISSN 2059-7983, Vol. 82, no 7, p. 715-726Article in journal (Refereed) Published
Abstract [en]

Time-resolved X-ray solution scattering (TR-XSS) enables tracking of protein structural dynamics but can suffer from radiation damage when performed with continuous X-ray beam exposure at multipurpose small-angle X-ray scattering (SAXS) beamlines. Here, we systematically assess how protein concentration, exposure time, X-ray dose and beam focusing influence the stability of adenylate kinase (AdK) during TR-XSS at CoSAXS at the MAX IV Laboratory. Static SAXS measurements from 2.5 to 21 mg ml−1 showed only minor interparticle effects, establishing suitable concentrations for TR-XSS. Under detector-focused conditions, AdK irradiated at room temperature remained stable up to 3.13 kGy, with consistent absolute and difference scattering profiles over 50 ms. In contrast, focusing the beam directly on the sample increased the absorbed dose to 21.3 kGy and produced clear signatures of radiation damage, which included low-q intensity loss and increasing deviation from the low-dose condition. These results identify practical system-specific dose limits and highlight beam focusing as a key determinant of sample integrity. The workflow presented here provides general guidelines for minimizing radiation artifacts in TR-XSS on multipurpose SAXS beamlines.

Place, publisher, year, edition, pages
International Union Of Crystallography, 2026
Keywords
time-resolved X-ray solution scattering, small-angle X-ray scattering, radiation damage, adenylate kinase, dose control.
National Category
Structural Biology
Identifiers
urn:nbn:se:umu:diva-256428 (URN)10.1107/s2059798326005164 (DOI)001810943800002 ()42283204 (PubMedID)2-s2.0-105043784734 (Scopus ID)
Funder
Swedish Research Council, 2024-04385The Kempe Foundations, JCSMK 24-543EU, Horizon 2020, 101081419
Note

This article is part of the Proceedings of the 12th International Workshop on X-ray Radiation Damage to Biological Crystalline Samples.

Available from: 2026-07-03 Created: 2026-07-03 Last updated: 2026-07-17Bibliographically approved
Magkakis, K., Orädd, F., Sabzian-Molaei, F., Levantino, M. & Andersson, M. Mapping microsecond conformational transitions in adenylate kinase.
Open this publication in new window or tab >>Mapping microsecond conformational transitions in adenylate kinase
Show others...
(English)Manuscript (preprint) (Other academic)
National Category
Biophysics
Identifiers
urn:nbn:se:umu:diva-251434 (URN)
Available from: 2026-03-27 Created: 2026-03-27 Last updated: 2026-03-31Bibliographically approved
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