Abstract

SummaryCryoelectron tomography (cryo-ET) and subtomogram averaging (STA) allow direct visualization and structural studies of biological macromolecules in their native cellular environment, in situ. Often, low signal-to-noise ratios in tomograms, low particle abundance within the cell, and low throughput in typical cryo-ET workflows severely limit the obtainable structural information. To help mitigate these limitations, here we apply a compressed sensing approach using 3D second-order total variation (CS-TV2) to tomographic reconstruction. We show that CS-TV2 increases the signal-to-noise ratio in tomograms, enhancing direct visualization of macromolecules, while preserving high-resolution information up to the secondary structure level. We show that, particularly with small datasets, CS-TV2 allows improvement of the resolution of STA maps. We further demonstrate that the CS-TV2 algorithm is applicable to cellular specimens, leading to increased visibility of molecular detail within tomograms. This work highlights the potential of compressed sensing-based reconstruction algorithms for cryo-ET and in situ structural biology.

Highlights

  • Cryoelectron tomography is an increasingly popular method for direct visualization of macromolecules in their native environment, which, together with subtomogram averaging (STA), allows structure determination of biological macromolecules (Beck and Baumeister, 2016; Briggs, 2013; Lucic et al, 2005; Wan and Briggs, 2016)

  • We provide a detailed comparison of compressed sensing (CS)-TV2 with weighted back-projection (WBP) using STA of purified specimens

  • We find that CS-TV2 outperforms WBP at small subtomogram numbers while providing comparable results for medium-sized datasets where secondary structure elements could be resolved

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Summary

SUMMARY

Cryoelectron tomography (cryo-ET) and subtomogram averaging (STA) allow direct visualization and structural studies of biological macromolecules in their native cellular environment, in situ. Low signal-tonoise ratios in tomograms, low particle abundance within the cell, and low throughput in typical cryo-ET workflows severely limit the obtainable structural information. To help mitigate these limitations, here we apply a compressed sensing approach using 3D second-order total variation (CS-TV2) to tomographic reconstruction. We show that CS-TV2 increases the signal-to-noise ratio in tomograms, enhancing direct visualization of macromolecules, while preserving high-resolution information up to the secondary structure level. This work highlights the potential of compressed sensingbased reconstruction algorithms for cryo-ET and in situ structural biology

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