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The advent of ultrabright fourth generation X-ray light sources, including X-ray free-electron lasers (XFELs) and diffraction limited synchrotrons, has significantly advanced the field of serial macromolecular protein crystallography (SX). SX experiments demand a continuous supply of fresh microcrystalline sample, ideally while minimizing overall sample consumption. Here, we introduce a novel, robust, and user-friendly polymer film technology that can be assembled in various configurations to encapsulate protein microcrystals and provide sample support for SX. This system provides an efficient hydration barrier over extended durations while maintaining an exceptionally low X-ray background. We have validated this technology by assessing hydration retention under both ambient and ultra-high vacuum conditions, and by evaluating its mechanical stability under XFEL pulses. Furthermore, we have demonstrated the effectiveness of this approach in two room-temperature serial crystallography studies to determine the structure of a 24 kDa Rapid Encystment Phenotype (REP24) protein from .
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http://dx.doi.org/10.1101/2025.07.13.663488 | DOI Listing |
bioRxiv
July 2025
Biosciences and Biotechnology Division, Physical and Life Sciences Directorate, Lawrence Livermore National Laboratory, Livermore, USA.
The advent of ultrabright fourth generation X-ray light sources, including X-ray free-electron lasers (XFELs) and diffraction limited synchrotrons, has significantly advanced the field of serial macromolecular protein crystallography (SX). SX experiments demand a continuous supply of fresh microcrystalline sample, ideally while minimizing overall sample consumption. Here, we introduce a novel, robust, and user-friendly polymer film technology that can be assembled in various configurations to encapsulate protein microcrystals and provide sample support for SX.
View Article and Find Full Text PDFIUCrJ
July 2025
Institut für Kernphysik, J. W. Goethe-Universität Frankfurt am Main, 60438 Frankfurt am Main, Germany.
We demonstrate an advanced scattering method for accessing the 3D reciprocal space of crystalline structures forming in a rapidly supercooled noble-gas liquid using a combination of femtosecond X-ray diffraction and X-ray cross-correlation analysis. The preservation of angular information from the scattering signal allows probing the structure factor along selected directions in reciprocal space and identifying signatures undetectable in azimuthally integrated scattering curves. Therefore, more information from serial diffraction experiments on stochastic crystallization processes can be retrieved despite the inherent variation of the crystal orientation and morphology for each single probe.
View Article and Find Full Text PDFProtein Sci
June 2025
Research Complex at Harwell, Scientific Computing Department, Science and Technology Facilities Council, Harwell, UK.
The rapid advancement of automatic structure solution methods, driven by the availability of high-quality predicted structures from AlphaFold and the growing adoption of multi-crystal and serial experiments, has created a pressing need for streamlining routine operations, automating structure solution projects, and efficiently handling large volumes of data. Modern software solutions must be both robust and user-friendly, supporting manual workflows while enabling high-throughput operations to keep pace with the high data collection rates of modern beamlines. Here, we present new developments in CCP4 Cloud that address these challenges by providing predefined and customizable automatic workflows, which can be seamlessly integrated with experimental facilities, offering a powerful solution for modern macromolecular crystallography.
View Article and Find Full Text PDFActa Crystallogr D Struct Biol
May 2025
Molecular Biophysics and Integrated Bioimaging Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.
Serial crystallography is an important technique with unique abilities to resolve enzymatic transition states, minimize radiation damage to sensitive metalloenzymes and perform de novo structure determination from micrometre-sized crystals. This technique requires the merging of data from thousands of crystals, making manual identification of errant crystals unfeasible. cctbx.
View Article and Find Full Text PDFIUCrJ
May 2025
Center for Free-Electron Laser Science CFEL, Deutsches Elektronen-Synchrotron DESY, Notkestr. 85, 22607 Hamburg, Germany.
Microcrystals are transforming structural biology by enabling high-resolution structures and time-resolved insights from samples once deemed too small. This commentary highlights recent advances in microfocus X-ray and MicroED methods, emphasizing their growing role as powerful and complementary tools in modern macromolecular crystallography.
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