Abstract

Validation is a necessity to trust the structures solved by electron microscopy by single particle techniques. The impressive achievements in single particle reconstruction fuel its expansion beyond a small community of image processing experts. This poses the risk of inappropriate data processing with dubious results. Nowhere is it more clearly illustrated than in the recovery of a reference density map from pure noise aligned to that map—a phantom in the noise. Appropriate use of existing validating methods such as resolution-limited alignment and the processing of independent data sets (“gold standard”) avoid this pitfall. However, these methods can be undermined by biases introduced in various subtle ways. How can we test that a map is a coherent structure present in the images selected from the micrographs? In stead of viewing the phantom emerging from noise as a cautionary tale, it should be used as a defining baseline. Any map is always recoverable from noise images, provided a sufficient number of images are aligned and used in reconstruction. However, with smaller numbers of images, the expected coherence in the real particle images should yield better reconstructions than equivalent numbers of noise or background images, even without masking or imposing resolution limits as potential biases. The validation test proposed is therefore a simple alignment of a limited number of micrograph and noise images against the final reconstruction as reference, demonstrating that the micrograph images yield a better reconstruction. I examine synthetic cases to relate the resolution of a reconstruction to the alignment error as a function of the signal-to-noise ratio. I also administered the test to real cases of publicly available data. Adopting such a test can aid the microscopist in assessing the usefulness of the micrographs taken before committing to lengthy processing with questionable outcomes.

Highlights

  • The biomedical community benefits enormously from fundamental knowledge of the structures of biomolecules and associated mechanisms of function

  • The contrast transfer function (CTF) was automatically determined for each micrograph and the particle and background images corrected by phase flipping and baseline adjustment using program bctf [9]

  • The resolution of a reconstruction is a function of the number of images contributing to it and the signal-to-noise ratio (SNR) of those images

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Summary

Introduction

The biomedical community benefits enormously from fundamental knowledge of the structures of biomolecules and associated mechanisms of function. The validity of these structures are of vital importance. In recent years cryo-electron microscopy (cryoEM) advanced to the point where 3D reconstructions can be interpreted at near-atomic resolution [1]. This enticement together with the ubiquity of good software for processing electron micrographs and doing single particle analysis (SPA) is driving its adoption in many laboratories. It is recognized with increased urgency that adequate validation methods are needed to accompany the maps derived from electron microscopy [2]

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