Shi D, Hsiung H H, Pace R C, Stokes D L
Department of Molecular Physiology and Biological Physics, University of Virginia Health Sciences Center, Charlottesville 22908, USA.
Biophys J. 1995 Mar;68(3):1152-62. doi: 10.1016/S0006-3495(95)80291-2.
Obtaining large, flat, well ordered crystals represents the key to structure determination by electron crystallography. Multilamellar crystals of Ca(2+)-ATPase are a good candidate for this methodology, and we have optimized methods of crystallization and of preparation for cryoelectron microscopy. In particular, high concentrations of glycerol were found to prevent nucleation and to reduce stacking; thus, by seeding solutions containing 40% glycerol, we obtained thin crystals that were 5-30 microns in diameter and 2-10 unit cells thick. We found that removing vesicles and minimizing concentrations of divalent cations were critical to preparing flat crystals in the frozen-hydrated state. Finally, we developed two methods for determining the number of lamellae composing individual crystals, information that is required for structure determination of this crystal form. The first method, using low magnification images of freeze-dried crystals, is more practical in our case. Nevertheless, the alternative method, involving analysis of Laue zones from electron diffraction patterns of slightly tilted crystals, may be of general use in structure determination from thin, three-dimensional crystals.
获得大尺寸、平整且有序排列的晶体是通过电子晶体学确定结构的关键。Ca(2+) -ATP酶的多层晶体是这种方法的理想候选对象,并且我们已经优化了结晶方法以及冷冻电子显微镜样品制备方法。特别地,发现高浓度甘油可防止成核并减少堆积;因此,通过在含有40%甘油的溶液中接种,我们获得了直径为5 - 30微米且厚度为2 - 10个晶胞的薄晶体。我们发现去除囊泡并将二价阳离子浓度降至最低对于制备处于冷冻水合状态的平整晶体至关重要。最后,我们开发了两种方法来确定构成单个晶体的片层数,这是确定这种晶体形式结构所需的信息。第一种方法是使用冻干晶体的低倍图像,在我们的情况下这种方法更实用。然而,另一种方法,即分析稍微倾斜晶体的电子衍射图案中的劳厄区,可能在从薄的三维晶体进行结构确定时具有普遍用途。