Jensen G J, Kornberg R D
Department of Structural Biology, Stanford University, School of Medicine, CA 94305, USA.
Ultramicroscopy. 2000 Jul;84(1-2):57-64. doi: 10.1016/s0304-3991(00)00005-x.
Three-dimensional reconstructions of icosahedral viruses from cryoelectron microscope images have reached resolutions where the microscope depth of field is a significant resolution-limiting factor. An analytical treatment presented here shows how the depth of field limitation can be understood as an envelope function which gradually attenuates the signal, starting well before the numerical depth of field is actually reached. A simple modification to the well-known back-projection reconstruction algorithm is described, called the defocus-gradient corrected back-projection, which computationally corrects for the contrast transfer function along a defocus gradient. Computer simulations demonstrate how the algorithm effectively eliminates the depth of field limitation.
从冷冻电子显微镜图像对二十面体病毒进行三维重建,已达到一定分辨率,此时显微镜的景深成为一个显著的分辨率限制因素。本文提出的一种分析方法表明,景深限制可理解为一种包络函数,它在实际达到数值景深之前就开始逐渐衰减信号。文中描述了对著名的反投影重建算法的一种简单修改,称为散焦梯度校正反投影,该方法通过计算沿散焦梯度校正对比度传递函数。计算机模拟展示了该算法如何有效消除景深限制。