Sander B, Golas M M, Stark H
Research Group of 3D Electron Cryomicroscopy, Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, 37077 Göttingen, Germany.
J Struct Biol. 2005 Jul;151(1):92-105. doi: 10.1016/j.jsb.2005.04.004.
For three-dimensional (3D) structure determination of large macromolecular complexes, single-particle electron cryomicroscopy is considered the method of choice. Within this field, structure determination de novo, as opposed to refinement of known structures, still presents a major challenge, especially for macromolecules without point-group symmetry. This is primarily because of technical issues: one of these is poor image contrast, and another is the often low particle concentration and sample heterogeneity imposed by the practical limits of biochemical purification. In this work, we tested a state-of-the art 4 k x 4 k charge-coupled device (CCD) detector (TVIPS TemCam-F415) to see whether or not it can contribute to improving the image features that are especially important for structure determination de novo. The present study is therefore focused on a comparison of film and CCD detector in the acquisition of images in the low-to-medium ( approximately 10-25 A) resolution range using a 200 kV electron microscope equipped with field emission gun. For comparison, biological specimens and radiation-insensitive carbon layers were imaged under various conditions to test the image phase transmission, spatial signal-to-noise ratio, visual image quality and power-spectral signal decay for the complete image-processing chain. At all settings of the camera, the phase transmission and spectral signal-to-noise ratio were significantly better on CCD than on film in the low-to-medium resolution range. Thus, the number of particle images needed for initial structure determination is reduced and the overall quality of the initial computed 3D models is improved. However, at high resolution, film is still significantly better than the CCD camera: without binning of the CCD camera and at a magnification of 70 kx, film is better beyond 21 A resolution. With 4-fold binning of the CCD camera and at very high magnification (> 300 kx) film is still superior beyond 7 A resolution.
对于大型大分子复合物的三维(3D)结构测定,单颗粒电子冷冻显微镜被认为是首选方法。在这个领域中,与已知结构的精修相反,从头开始测定结构仍然是一个重大挑战,特别是对于没有点群对称性的大分子。这主要是由于技术问题:其中之一是图像对比度差,另一个是生化纯化的实际限制所导致的颗粒浓度常常较低以及样品的异质性。在这项工作中,我们测试了一种先进的4k×4k电荷耦合器件(CCD)探测器(TVIPS TemCam-F415),以了解它是否有助于改善对于从头开始结构测定特别重要的图像特征。因此,本研究聚焦于在配备场发射枪的200 kV电子显微镜下,比较胶片和CCD探测器在低至中(约10 - 25 Å)分辨率范围内采集图像的情况。为了进行比较,在各种条件下对生物标本和抗辐射的碳层进行成像,以测试完整图像处理链的图像相位传递、空间信噪比、视觉图像质量和功率谱信号衰减。在相机的所有设置下,在低至中分辨率范围内,CCD上的相位传递和光谱信噪比明显优于胶片。因此,初始结构测定所需的颗粒图像数量减少,并且初始计算的3D模型的整体质量得到提高。然而,在高分辨率下,胶片仍然明显优于CCD相机:在不进行CCD相机合并且放大倍数为70 kx时,胶片在分辨率超过21 Å时表现更好。在对CCD相机进行4倍合并且放大倍数非常高(> 300 kx)时,胶片在分辨率超过7 Å时仍然更优。