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Solution x-ray scattering-based estimation of electron cryomicroscopy imaging parameters for reconstruction of virus particles.

机译:基于解决方案X射线散射的电子冷冻显微镜成像参数估计,用于病毒颗粒的重建。

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摘要

Structure factor amplitudes and phases can be computed directly from electron cryomicroscopy images. Inherent aberrations of the electromagnetic lenses and other instrumental factors affect the structure factors, however, resulting in decreased accuracy in the determined three-dimensional reconstruction. In contrast, solution x-ray scattering provides absolute and accurate measurement of spherically averaged structure factor amplitudes of particles in solution but does not provide information on the phases. In the present study, we explore the merits of using solution x-ray scattering data to estimate the imaging parameters necessary to make corrections to the structure factor amplitudes derived from electron cryomicroscopic images of icosahedral virus particles. Using 400-kV spot-scan images of the bacteriophage P22 procapsid, we have calculated an amplitude contrast of 8.0 +/- 5.2%. The amplitude decay parameter has been estimated to be 523 +/- 188 A2 with image noise compensation and 44 +/- 66 A2 without it. These results can also be used to estimate the minimum number of virus particles needed for reconstruction at different resolutions.
机译:结构因子的幅值和相位可以直接从电子显微镜检查图像中计算出来。但是,电磁透镜的固有像差和其他仪器因素会影响结构因素,从而导致确定的三维重构的准确性降低。相反,溶液X射线散射提供了溶液中颗粒的球形平均结构因子振幅的绝对,准确的测量结果,但没有提供有关相的信息。在本研究中,我们探讨了使用溶液X射线散射数据来估算对二十面体病毒颗粒的电子冷冻显微镜图像得出的结构因子振幅进行校正所必需的成像参数的优点。使用噬菌体P22衣壳的400 kV点扫描图像,我们计算出8.0 +/- 5.2%的幅度对比度。带有图像噪声补偿的幅度衰减参数估计为523 +/- 188 A2,不带图像噪声补偿的估计为44 +/- 66 A2。这些结果还可以用于估计在不同分辨率下重建所需的最小病毒颗粒数。

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