Abstract
Three-dimensional (3D) reconstruction in single-particle cryo-electron microscopy (cryo-EM) is a significant technique for recovering the 3D structure of proteins or other biological macromolecules from their two-dimensional (2D) noisy projection images taken from unknown random directions. Class averaging in single-particle cryo-EM is an important procedure for producing high-quality initial 3D structures, where image alignment is a fundamental step. In this paper, an efficient image alignment algorithm using 2D interpolation in the frequency domain of images is proposed to improve the estimation accuracy of alignment parameters of rotation angles and translational shifts between the two projection images, which can obtain subpixel and subangle accuracy. The proposed algorithm firstly uses the Fourier transform of two projection images to calculate a discrete cross-correlation matrix and then performs the 2D interpolation around the maximum value in the cross-correlation matrix. The alignment parameters are directly determined according to the position of the maximum value in the cross-correlation matrix after interpolation. Furthermore, the proposed image alignment algorithm and a spectral clustering algorithm are used to compute class averages for single-particle 3D reconstruction. The proposed image alignment algorithm is firstly tested on a Lena image and two cryo-EM datasets. Results show that the proposed image alignment algorithm can estimate the alignment parameters accurately and efficiently. The proposed method is also used to reconstruct preliminary 3D structures from a simulated cryo-EM dataset and a real cryo-EM dataset and to compare them with RELION. Experimental results show that the proposed method can obtain more high-quality class averages than RELION and can obtain higher reconstruction resolution than RELION even without iteration.
Highlights
IntroductionThree-dimensional (3D) reconstruction in single-particle cryo-electron microscopy (cryoEM) is a significant technique for recovering the 3D structure of proteins or other biological macromolecules from their two-dimensional (2D) noisy projection images taken from unknown random directions
In the single-particle reconstruction, the same macromolecule is projected from various unknown directions, and the final 3D structure of the macromolecule can be reconstructed from the two-dimensional (2D) projection images using the estimated projection directions in 3D
Due to the very low signal-to-noise ratio (SNR) of the projection images caused by low-dose electron radiation, it is usually difficult to obtain the correct estimation of the projection directions
Summary
Three-dimensional (3D) reconstruction in single-particle cryo-electron microscopy (cryoEM) is a significant technique for recovering the 3D structure of proteins or other biological macromolecules from their two-dimensional (2D) noisy projection images taken from unknown random directions. Cryo-electron microscopy (cryo-EM) has become a recognized powerful technique in structural biology for three-dimensional (3D) structure determination of biological macromolecules, supramolecular complexes, and subcellular structures [1,2,3]. It does not need crystallization and has been widely used to study large macromolecular complexes that are difficult to be crystallized.
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