首页> 外文期刊>Journal of Structural Biology >PRACTICAL IMAGE RESTORATION OF THICK BIOLOGICAL SPECIMENS USING MULTIPLE FOCUS LEVELS IN TRANSMISSION ELECTRON MICROSCOPY
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PRACTICAL IMAGE RESTORATION OF THICK BIOLOGICAL SPECIMENS USING MULTIPLE FOCUS LEVELS IN TRANSMISSION ELECTRON MICROSCOPY

机译:透射电子显微镜中使用多个焦点水平的厚生物样本的实用图像恢复

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Three-dimensional electron tomographic studies of thick specimens such as cellular organelles or supramolecular structures require accurate interpretations of transmission electron micrograph intensities. In addition to microscope lens aberrations, thick specimen imaging is complicated by additional distortions resulting from multiple elastic and inelastic scattering. Extensive analysis of the mechanism of image formation using electron energy-loss spectroscopy and imaging as well as exit wavefront reconstruction demonstrated that multiple scattering does not contribute to the coherent component of the exit wave (Han et al., 1996, 1995). Although exit wavefront restored images showed enhanced contrast and resolution, that technique, which requires the collection of more than 30 images at different focus levels, is not practical for routine data collection in 3D electron tomography, where usually over 100 projection views are required for each reconstruction, Using a 0.7-mu m-thick specimen imaged at 200 keV, the accuracy of reconstructions using small numbers of defocused images and a simple linear filter (Schiske, 1968) was assessed by comparison to the complete exit wave restoration. We demonstrate that only four optimal focus levels are required to effectively restore the coherent component (deviation 5.1%). By contrast, the optimal single image (zero defocus) shows a 25.5% deviation to the exit wave restoration. Two pairs of under-and over-defocus images should be taken: one pair at quite high defocus (>10 mu m) to differentiate the coherent (single elastic scattering) from the incoherent (multiple elastic and inelastic scattering) components, and the second pair to optimize information content at the highest desired resolution (e.g., 5 mu m for (2.5 nm)(-1) resolution). We also propose a new interpretation of the restored amplitude and phase components where the specimen mass-density is proportional to the logarithm of the amplitude component and linearly related to the phase component, This approach should greatly facilitate the collection of high resolution tomographic data from thick samples. (C) 1997 Academic Press. [References: 22]
机译:厚样品(例如细胞器或超分子结构)的三维电子断层扫描研究需要对透射电子显微照片强度进行准确的解释。除了显微镜透镜的像差之外,由于多次弹性和非弹性散射而导致的其他扭曲也会使厚样本成像变得复杂。使用电子能量损失谱和成像以及出射波前重建对成像机制的广泛分析表明,多重散射对出射波的相干成分没有贡献(Han et al。,1996,1995)。尽管出射波前恢复的图像显示出增强的对比度和分辨率,但是该技术需要在不同的聚焦级别上收集30多个图像,对于3D电子断层扫描中的常规数据收集来说并不实用,因为通常每个图像都需要100多个投影视图重建,使用200 keV成像的0.7微米厚的样本,通过与完整的出射波恢复进行比较,评估了使用少量散焦图像和简单的线性滤波器(Schiske,1968)的重建精度。我们证明,仅需要四个最佳聚焦水平即可有效地恢复相干分量(偏差为5.1%)。相比之下,最佳的单张图像(零散焦)显示出出射波恢复偏差25.5%。应该拍摄两对散焦不足和散焦图像:一对散焦非常高(> 10μm),以将相干分量(单个弹性散射)与非相干分量(多个弹性散射和非弹性散射)区分开来;配对以最理想的分辨率(例如,对于(2.5 nm)(-1)分辨率为5微米)优化信息内容。我们还对恢复的振幅和相位分量提出了新的解释,其中样品质量密度与振幅分量的对数成正比,并且与相位分量线性相关。这种方法应该极大地方便从厚层收集高分辨率的层析成像数据样品。 (C)1997学术出版社。 [参考:22]

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