$\gamma$-SUP: A clustering algorithm for cryo-electron microscopy images of asymmetric particles

TL;DR

The paper introduces $oldsymbol{ extgamma}$-SUP, a robust clustering algorithm for cryo-EM images that improves 3D structure reconstruction by effectively handling noise, high dimensionality, and misalignments.

Contribution

The paper presents $oldsymbol{ extgamma}$-SUP, a novel clustering method based on $q$-Gaussian mixtures and $oldsymbol{ extgamma}$-divergence, tailored for cryo-EM data with outliers and misalignments.

Findings

$oldsymbol{ extgamma}$-SUP outperforms existing methods in robustness to misalignment outliers.

Application to real cryo-EM data reveals true structural features of ribosome.

Method effectively reduces noise in projections to aid 3D reconstruction.

Abstract

Cryo-electron microscopy (cryo-EM) has recently emerged as a powerful tool for obtaining three-dimensional (3D) structures of biological macromolecules in native states. A minimum cryo-EM image data set for deriving a meaningful reconstruction is comprised of thousands of randomly orientated projections of identical particles photographed with a small number of electrons. The computation of 3D structure from 2D projections requires clustering, which aims to enhance the signal to noise ratio in each view by grouping similarly oriented images. Nevertheless, the prevailing clustering techniques are often compromised by three characteristics of cryo-EM data: high noise content, high dimensionality and large number of clusters. Moreover, since clustering requires registering images of similar orientation into the same pixel coordinates by 2D alignment, it is desired that the clustering algorithm can label misaligned images as outliers. Herein, we introduce a clustering algorithm $\gamma$-SUP to model the data with a $q$-Gaussian mixture and adopt the minimum $\gamma$-divergence for estimation, and then use a self-updating procedure to obtain the numerical solution. We apply $\gamma$-SUP to the cryo-EM images of two benchmark macromolecules, RNA polymerase II and ribosome. In the former case, simulated images were chosen to decouple clustering from alignment to demonstrate $\gamma$-SUP is more robust to misalignment outliers than the existing clustering methods used in the cryo-EM community. In the latter case, the clustering of real cryo-EM data by our $\gamma$-SUP method eliminates noise in many views to reveal true structure features of ribosome at the projection level.