Zhu J, Penczek P A, Schröder R, Frank J
Wadsworth Center, New York State Department of Health, Albany 12201-0509, USA.
J Struct Biol. 1997 Apr;118(3):197-219. doi: 10.1006/jsbi.1997.3845.
Cryoelectron microscopy provides the means of studying macromolecules in their native state. However, the contrast transfer function (CTF) makes the images and the three-dimensional (3D) maps derived from them difficult to interpret. We developed methods to determine the CTF from experimental data and to obtain a CTF-corrected 3D reconstruction. The CTF correction and 3D reconstruction accomplished in one step make it easy to combine different defocus data sets and decrease the error accumulation in the computation. These methods were applied to energy-filtered images of the 70S Escherichia coli ribosome, resulting in a distortion-free 3D map of the ribosome at 1/24.5 A-1 resolution, as determined by the differential phase residual resolution criterion.
冷冻电子显微镜提供了在天然状态下研究大分子的方法。然而,对比度传递函数(CTF)使得从其获得的图像和三维(3D)图谱难以解释。我们开发了从实验数据确定CTF并获得经CTF校正的3D重建的方法。一步完成的CTF校正和3D重建使得组合不同散焦数据集变得容易,并减少了计算中的误差积累。这些方法应用于70S大肠杆菌核糖体的能量过滤图像,根据差分相位残余分辨率标准确定,得到了分辨率为1/24.5 Å-1的无扭曲核糖体3D图谱。