Ravelli Raimond B G, Haselmann-Weiss Uta, McGeehan John E, McCarthy Andrew A, Marquez Josan A, Antony Claude, Frangakis Achilleas S, Stranzl Gudrun
EMBL Grenoble, 6 rue Jules Horowitz, BP 181, 38042 Grenoble CEDEX 9, France.
J Synchrotron Radiat. 2007 Jan;14(Pt 1):128-32. doi: 10.1107/S0909049506043111. Epub 2006 Dec 15.
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.
快速玻璃化,随后用溶剂取代玻璃化水(冷冻置换),然后用树脂处理,这是一种广泛用于制备用于电子显微镜检查的生物样品的方法。所得的塑料包埋样品便于在室温下切片(切片术),并且可以产生保存良好的细胞结构。在这里,该方法已应用于结晶蛋白质样品,结果表明,可以在冷冻置换玻璃化晶体的同时保留其一些原始衍射特性。塑料包埋的晶体用于在强大的大分子晶体学同步加速器光束线上收集一系列完整的室温数据集。虽然通常在X射线辐射下会观察到二硫键受到特定损伤,但对于塑料包埋的样品却未观察到这种损伤。X射线衍射数据允许对冷冻置换和塑料包埋对生物样品的影响进行初步的原子分析。