Abstract

BackgroundIdentification and selection of protein particles in cryo-electron micrographs is an important step in single particle analysis. In this study, we developed a deep learning-based particle picking network to automatically detect particle centers from cryoEM micrographs. This is a challenging task due to the nature of cryoEM data, having low signal-to-noise ratios with variable particle sizes, shapes, distributions, grayscale variations as well as other undesirable artifacts.ResultsWe propose a double convolutional neural network (CNN) cascade for automated detection of particles in cryo-electron micrographs. This approach, entitled Deep Regression Picker Network or “DRPnet”, is simple but very effective in recognizing different particle sizes, shapes, distributions and grayscale patterns corresponding to 2D views of 3D particles. Particles are detected by the first network, a fully convolutional regression network (FCRN), which maps the particle image to a continuous distance map that acts like a probability density function of particle centers. Particles identified by FCRN are further refined to reduce false particle detections by the second classification CNN. DRPnet’s first CNN pretrained with only a single cryoEM dataset can be used to detect particles from different datasets without retraining. Compared to RELION template-based autopicking, DRPnet results in better particle picking performance with drastically reduced user interactions and processing time. DRPnet also outperforms the state-of-the-art particle picking networks in terms of the supervised detection evaluation metrics recall, precision, and F-measure. To further highlight quality of the picked particle sets, we compute and present additional performance metrics assessing the resulting 3D reconstructions such as number of 2D class averages, efficiency/angular coverage, Rosenthal-Henderson plots and local/global 3D reconstruction resolution.ConclusionDRPnet shows greatly improved time-savings to generate an initial particle dataset compared to manual picking, followed by template-based autopicking. Compared to other networks, DRPnet has equivalent or better performance. DRPnet excels on cryoEM datasets that have low contrast or clumped particles. Evaluating other performance metrics, DRPnet is useful for higher resolution 3D reconstructions with decreased particle numbers or unknown symmetry, detecting particles with better angular orientation coverage.

Highlights

  • Identification and selection of protein particles in cryo-electron micrographs is an important step in single particle analysis

  • In summary, we propose a Deep Regression Picker Network (DRPnet) and successfully demonstrate the ability to pick particles on a multiple datasets of cryo-EM micrographs which is different from the training data (TRPV1,EMPIAR-10017)—different sized/ shaped/separated particles, collected on different microscopes, using different cameras, with different background contrast—and greatly reduced the timeconsuming barrier of manual picking to generate a template

  • Compared to other deep learning tools for particle picking of cryo-electron microscopy (cryoEM) micrographs reported to date, this cascade strategy is unique

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Summary

Introduction

Identification and selection of protein particles in cryo-electron micrographs is an important step in single particle analysis. High resolution 3D protein structure determination via single particle analysis ( known as single particle reconstruction) using cryo-electron microscopy (cryoEM) is becoming more widely used, it still remains to be a challenging technique because of the resulting noisy and often low contrast micrographs [1, 2]. In these cryoEM experiments, a purified, homogeneous protein is vitreously frozen in a thin film of solution to form a glass-like ice, which is imaged under cryogenic temperatures (− 170 ◦C ) in a transmission electron microscope (TEM) [3]. These solutions require large numbers of particles to accurately estimate the relative angular orientations of these protein particles in 3D, which is used to create 3D reconstructions of averaged protein particle structures

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