Abstract

Single Particle Analysis using cryo-electron microscopy is a structural biology technique aimed at capturing the three-dimensional (3D) conformation of biological macromolecules. Projection images used to construct the 3D density map are characterized by a very low signal-to-noise ratio to minimize radiation damage in the samples. As a consequence, the 3D image alignment process is a challenging and error prone task which usually determines the success or failure of obtaining a high quality map. In this work, we present an approach able to quantify the alignment precision and accuracy of the 3D alignment process, which is then being used to help the reconstruction process in a number of ways, such as: (1) Providing quality indicators of the macromolecular map for soft validation, (2) Assessing the degree of homogeneity of the sample and, (3), Selecting subsets of representative images. We present experimental results in which the quality of the finally obtained 3D maps is clearly improved.

Highlights

  • Understanding how macromolecular complexes fulfill their complicated roles in the living cell is a central theme in molecular biology

  • The approach is based on three steps that should be run for each particle: alignment precision estimation, alignment accuracy estimation, and determination of the percentage of reliable particles (Q value)

  • We propose a novel method to perform quantitative analysis of the 3D alignment quality, which can be used to: (1) soft-validation of cryo-EM determined structures, (2) particle ranking and pruning and (3) data homogeneity analysis

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Summary

Introduction

Understanding how macromolecular complexes fulfill their complicated roles in the living cell is a central theme in molecular biology. 15 an approach is proposed to determine the alignment precision of a set of particles used in the map reconstruction process.

Results
Conclusion
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