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用于冷冻电子断层扫描中异质子体积的 3D 配准和分类的协作框架。

A collaborative framework for 3D alignment and classification of heterogeneous subvolumes in cryo-electron tomography.

机构信息

Office of High Performance Computing and Communications, National Library of Medicine, National Institutes of Health, Bethesda, MD 20894, USA.

出版信息

J Struct Biol. 2013 Feb;181(2):116-27. doi: 10.1016/j.jsb.2012.10.010. Epub 2012 Oct 27.

Abstract

The limitation of using low electron doses in non-destructive cryo-electron tomography of biological specimens can be partially offset via averaging of aligned and structurally homogeneous subsets present in tomograms. This type of sub-volume averaging is especially challenging when multiple species are present. Here, we tackle the problem of conformational separation and alignment with a "collaborative" approach designed to reduce the effect of the "curse of dimensionality" encountered in standard pair-wise comparisons. Our new approach is based on using the nuclear norm as a collaborative similarity measure for alignment of sub-volumes, and by exploiting the presence of symmetry early in the processing. We provide a strict validation of this method by analyzing mixtures of intact simian immunodeficiency viruses SIV mac239 and SIV CP-MAC. Electron microscopic images of these two virus preparations are indistinguishable except for subtle differences in conformation of the envelope glycoproteins displayed on the surface of each virus particle. By using the nuclear norm-based, collaborative alignment method presented here, we demonstrate that the genetic identity of each virus particle present in the mixture can be assigned based solely on the structural information derived from single envelope glycoproteins displayed on the virus surface.

摘要

在对生物标本进行非破坏性低温电子断层扫描时,使用低电子剂量的限制可以通过对断层图像中存在的对齐且结构均匀的子集中进行平均来部分抵消。当存在多种物质时,这种类型的子体积平均特别具有挑战性。在这里,我们通过设计一种“协作”方法来解决构象分离和对准的问题,该方法旨在减少标准两两比较中遇到的“维度诅咒”的影响。我们的新方法基于使用核范数作为子体积对齐的协作相似性度量,并利用处理过程早期存在的对称性。我们通过分析完整的猴免疫缺陷病毒 SIV mac239 和 SIV CP-MAC 的混合物来严格验证这种方法。这两种病毒制剂的电子显微镜图像无法区分,除了每个病毒颗粒表面展示的包膜糖蛋白构象的细微差异。通过使用这里提出的基于核范数的协作对准方法,我们证明可以仅基于从病毒表面展示的单个包膜糖蛋白得出的结构信息来分配混合物中存在的每个病毒颗粒的遗传身份。

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