Multiscale reconstruction of protein conformations from cryo-EM images
Abstract
We present a novel multiscale algorithm for directly recovering the atomic model structure of a protein from single-particle cryo-EM data. Our algorithm is able to estimate protein structures to state-of-the-art accuracy for high-noise and low-contrast data. It is also robust to misspecifications in the TEM image formation model. These desirable properties are primarily due to the use of an explicit representation of the protein backbone in terms of bonds, torsion angles and bond angles, which s...
Description / Details
We present a novel multiscale algorithm for directly recovering the atomic model structure of a protein from single-particle cryo-EM data. Our algorithm is able to estimate protein structures to state-of-the-art accuracy for high-noise and low-contrast data. It is also robust to misspecifications in the TEM image formation model. These desirable properties are primarily due to the use of an explicit representation of the protein backbone in terms of bonds, torsion angles and bond angles, which supplies rich prior information to the structure recovery process. We apply our method on three protein cryo-EM datasets, generated using an electron microscope digital twin, and show that using a multiscale approach yields an improvement of the root-mean-square deviation (RMSD) and template modelling (TM) scores with respect to the ground truth. Furthermore, there is evidence that larger-scale structures are being prioritised with the multiscale algorithm, which reduces the possibility of convergence to bad local minima.
Source: arXiv:2606.18058v1 - http://arxiv.org/abs/2606.18058v1 PDF: https://arxiv.org/pdf/2606.18058v1 Original Link: http://arxiv.org/abs/2606.18058v1
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Jun 17, 2026
Biomedical Engineering
Engineering
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