Gradient-based high precision alignment of cryo-electron subtomograms.

Min Xu, Frank Alber
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引用次数: 3

Abstract

Whole cell cryo-electron tomography emerges as an important component for structural system biology approaches. It allows the localization and structural characterization of macromolecular complexes in near living conditions. However, the method is hampered by low resolution, missing data and low signal-to-noise ratio (SNR). To overcome some of these difficulties one can align and average a large set of subtomograms. Existing alignment methods are mostly based on an exhaustive scanning and sampling of all but discrete relative rotations and translations of one subtomogram with respect to the other. In this paper, we propose a gradient-guided alignment method based on two subtomogram similarity measures. We also propose a stochastic parallel optimization that increases significantly the efficiency for the simultaneous refinement of a set of alignment candidates. Results on simulated data of model complexes and experimental structures of protein complexes show that even for highly distorted subtomograms and with only a small number of very sparsely distributed initial alignment seeds, our method can accurately recover true transformations with a significantly higher precision than scanning based alignment methods.

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基于梯度的低温电子亚层图高精度对准。
全细胞低温电子断层扫描是结构系统生物学研究的重要组成部分。它允许在近生活条件下大分子复合物的定位和结构表征。但该方法存在分辨率低、数据缺失、信噪比低等问题。为了克服这些困难,可以对大量的子层析图进行对齐和平均。现有的对准方法大多是基于对一个子层析图相对于另一个子层析图的相对旋转和平移进行详尽的扫描和采样。本文提出了一种基于两个子层析图相似性度量的梯度制导对准方法。我们还提出了一种随机并行优化方法,该方法显著提高了一组对齐候选者同时优化的效率。模型复合物的模拟数据和蛋白质复合物的实验结构结果表明,即使对于高度扭曲的亚层图,并且只有少量非常稀疏分布的初始定位种子,我们的方法也能准确地恢复真实的转换,其精度明显高于基于扫描的定位方法。
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