Extensive Angular Sampling Enables the Sensitive Localization of Macromolecules in Electron Tomograms

被引:31
作者
Chaillet, Marten L. [1 ]
van der Schot, Gijs [1 ]
Gubins, Ilja [2 ]
Roet, Sander [1 ]
Veltkamp, Remco C. [2 ]
Forster, Friedrich [1 ]
机构
[1] Univ Utrecht, Bijvoet Ctr Biomol Res, Struct Biochem, NL-3584 CG Utrecht, Netherlands
[2] Univ Utrecht, Dept Informat & Comp Sci, NL-3584 CC Utrecht, Netherlands
关键词
electron cryo-tomography; particle localization and identification; template matching; GPU acceleration; volume registration; BEAM-INDUCED MOTION; CRYOELECTRON TOMOGRAPHY; MOLECULAR SOCIOLOGY; COMPLEX; CELLS;
D O I
10.3390/ijms241713375
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cryo-electron tomography provides 3D images of macromolecules in their cellular context. To detect macromolecules in tomograms, template matching (TM) is often used, which uses 3D models that are often reliable for substantial parts of the macromolecules. However, the extent of rotational searches in particle detection has not been investigated due to computational limitations. Here, we provide a GPU implementation of TM as part of the PyTOM software package, which drastically speeds up the orientational search and allows for sampling beyond the Crowther criterion within a feasible timeframe. We quantify the improvements in sensitivity and false-discovery rate for the examples of ribosome identification and detection. Sampling at the Crowther criterion, which was effectively impossible with CPU implementations due to the extensive computation times, allows for automated extraction with high sensitivity. Consequently, we also show that an extensive angular sample renders 3D TM sensitive to the local alignment of tilt series and damage induced by focused ion beam milling. With this new release of PyTOM, we focused on integration with other software packages that support more refined subtomogram-averaging workflows. The automated classification of ribosomes by TM with appropriate angular sampling on locally corrected tomograms has a sufficiently low false-discovery rate, allowing for it to be directly used for high-resolution averaging and adequate sensitivity to reveal polysome organization.
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页数:19
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