Freeze electron cross-sectional image-oriented mismatching removal method

Abstract

The invention discloses a frozen electron cross-sectional image-oriented mismatching removal method, which comprises the following steps of: S1, screening stable matching from a group of frozen electron cross-sectional image pairs, and extracting motion information between feature points as a training sample; s2, inputting the training sample obtained in the S1 into a pre-constructed nonlinear regression model, and fitting an identification function for calculating all matching correctness probabilities of the frozen electron cross-sectional image pair through training; s3, an identification function is obtained based on training fitting in the S2, and the frozen electron cross-sectional image pair is calculated to obtain an initial matching group; s4, repeating S1, S2 and S3 until an initial matching group of all the frozen electron cross-sectional image pairs is obtained; and S5, on the basis of all the initial matching groups, finishing final mismatching removal work through an RANSAC (Random Sample Consensus) algorithm. According to the method, the wrong matching is removed by using the motion consistency between the electron tomography projection image sequences, so that the correct matching between the images is effectively kept, and meanwhile, the accuracy of the alignment result is improved.

Description

technical field

[0001] The invention relates to the technical field of structural biology, in particular to a method for removing mismatches for frozen electron tomography images. Background technique

[0002] Cryo-electron microscopy combined with three-dimensional reconstruction technology has developed rapidly in the field of structural biology in recent years and is making important breakthroughs. Compared with traditional methods such as X-ray crystallography and nuclear magnetic resonance spectroscopy to determine the three-dimensional structure of protein molecules, it has the following advantages: Several advantages:

[0003] 1. Maintain the activity and functional status of biological samples;

[0004] 2. There is no need to prepare crystals, especially suitable for the determination of the three-dimensional structure of macromolecules and their complexes that are difficult to crystallize;

[0005] 3. Combined with new equipment and technologies such as electron m...

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