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Visualization of protein crystals by high-energy phase-contrast X-ray imaging.


ABSTRACT: For the extraction of the best possible X-ray diffraction data from macromolecular crystals, accurate positioning of the crystals with respect to the X-ray beam is crucial. In addition, information about the shape and internal defects of crystals allows the optimization of data-collection strategies. Here, it is demonstrated that the X-ray beam available on the macromolecular crystallography beamline P14 at the high-brilliance synchrotron-radiation source PETRA III at DESY, Hamburg, Germany can be used for high-energy phase-contrast microtomography of protein crystals mounted in an optically opaque lipidic cubic phase matrix. Three-dimensional tomograms have been obtained at X-ray doses that are substantially smaller and on time scales that are substantially shorter than those used for diffraction-scanning approaches that display protein crystals at micrometre resolution. Adding a compound refractive lens as an objective to the imaging setup, two-dimensional imaging at sub-micrometre resolution has been achieved. All experiments were performed on a standard macromolecular crystallography beamline and are compatible with standard diffraction data-collection workflows and apparatus. Phase-contrast X-ray imaging of macromolecular crystals could find wide application at existing and upcoming low-emittance synchrotron-radiation sources.

SUBMITTER: Polikarpov M 

PROVIDER: S-EPMC6834075 | biostudies-literature | 2019 Nov

REPOSITORIES: biostudies-literature

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Visualization of protein crystals by high-energy phase-contrast X-ray imaging.

Polikarpov Maxim M   Bourenkov Gleb G   Snigireva Irina I   Snigirev Anatoly A   Zimmermann Sophie S   Csanko Krisztian K   Brockhauser Sandor S   Schneider Thomas R TR  

Acta crystallographica. Section D, Structural biology 20191031 Pt 11


For the extraction of the best possible X-ray diffraction data from macromolecular crystals, accurate positioning of the crystals with respect to the X-ray beam is crucial. In addition, information about the shape and internal defects of crystals allows the optimization of data-collection strategies. Here, it is demonstrated that the X-ray beam available on the macromolecular crystallography beamline P14 at the high-brilliance synchrotron-radiation source PETRA III at DESY, Hamburg, Germany can  ...[more]

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