Rapid vitrification followed by the replacement of the vitrified water by a solvent (freeze substitution) and then resin is a widely used procedure for preparing biological samples for electron microscopy. The resulting plastic-embedded samples permit convenient room-temperature sectioning (microtomy) and can yield well preserved cellular structures. Here this procedure has been applied to crystalline protein samples, and it is shown that it is possible to freeze-substitute vitrified crystals while preserving some of their original diffraction properties. The plastic-embedded crystals were used to collect a series of complete room-temperature data sets at a powerful macromolecular crystallography synchrotron beamline. Whereas one normally observes specific damage to disulfide bonds upon X-ray radiation, no such damage was seen for the plastic-embedded sample. The X-ray diffraction data allowed an initial atomic analysis to be made of the effects of freeze-substitution and plastic embedding on biological samples. © 2007 International Union of Crystallography Printed in Singapore - all rights reserved.
CITATION STYLE
Ravelli, R. B. G., Haselmann-Weiss, U., McGeehan, J. E., McCarthy, A. A., Marquez, J. A., Antony, C., … Stranzl, G. (2007). Plastic-embedded protein crystals. In Journal of Synchrotron Radiation (Vol. 14, pp. 128–132). https://doi.org/10.1107/S0909049506043111
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