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A multiresolution approach to the 3D reconstruction of a 50S ribosome from an EM-tilt series solving the alignment problem without gold particles (electron microscopy)

机译:从EM-倾斜系列对50S核糖体进行3D重建的多分辨率方法,解决了没有金颗粒的对准问题(电子显微镜)

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A multiresolution approach to 3D reconstruction from an electron microscope (EM) tilt series is presented. It is designed for reconstruction from a tilt series with a limited number of projections where the tilt angles are assumed to be known. Its main feature is that it solves the alignment problem very accurately from the image data without additional gold particles, including the determination of translational, orientational, and scaling parameters. The approach relies on a coarse-to-fine bootstrap control strategy based on the observation that with an appropriate matching procedure good alignment estimates can be obtained at a rather coarse level of resolution. This serves for a better reconstruction of the next finer level, from which a further refinement of the alignment estimate is obtained, etc. The actual reconstruction at each level of resolution is accomplished with a synthesis of the filtered back-projection method and iterative algebraic techniques, together with a set of convex constraints. The complete algorithm is applied to an EM tilt series of a 50S ribosome prepared in ice, consisting of 11 micrographs.
机译:提出了一种从电子显微镜(EM)倾斜系列进行3D重建的多分辨率方法。它设计用于从具有有限数量的投影的倾斜系列进行重建,其中假定倾斜角是已知的。它的主要特征是它可以从图像数据中非常精确地解决对齐问题,而无需使用其他金颗粒,包括确定平移,方向和缩放参数。该方法基于以下观察:从粗到细的自举控制策略,该观察结果是,通过适当的匹配过程,可以在相当粗略的分辨率级别上获得良好的对齐估计。这有助于更好地重建下一个更精细的层次,从而可以进一步优化对齐估计,依此类推。在每个分辨率层次上的实际重建都是通过滤波反投影方法和迭代代数技术的综合来完成的。 ,以及一组凸约束。完整的算法应用于由冰制成的50S核糖体的EM倾斜序列,该序列由11张显微照片组成。

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