Author: Ranno, Nathan; Si, Dong
                    Title: Neural Representations of Cryo-EM Maps and a Graph-Based Interpretation  Cord-id: aafnp3db  Document date: 2021_4_3
                    ID: aafnp3db
                    
                    Snippet: Advances in imagery at atomic and near-atomic resolution, such as cryogenic electron microscopy (cryo-EM), have led to an influx of high resolution images of proteins and other macromolecular structures to data banks worldwide. Producing a protein structure from the discrete voxel grid data of cryo-EM maps involves interpolation into the continuous spatial domain. We present a novel data format called the neural cryo-EM map, which is formed from a set of neural networks that accurately parameter
                    
                    
                    
                     
                    
                    
                    
                    
                        
                            
                                Document: Advances in imagery at atomic and near-atomic resolution, such as cryogenic electron microscopy (cryo-EM), have led to an influx of high resolution images of proteins and other macromolecular structures to data banks worldwide. Producing a protein structure from the discrete voxel grid data of cryo-EM maps involves interpolation into the continuous spatial domain. We present a novel data format called the neural cryo-EM map, which is formed from a set of neural networks that accurately parameterize cryo-EM maps and provide native, spatially continuous data for density and gradient. As a case study of this data format, we create graph-based interpretations of high resolution experimental cryo-EM maps. Normalized cryo-EM map values interpolated using the non-linear neural cryo-EM format are more accurate, consistently scoring less than 0.01 mean absolute error, than a conventional tri-linear interpolation, which scores up to 0.12 mean absolute error. Our graph-based interpretations of 115 experimental cryo-EM maps from 1.15 to 4.0 Angstrom resolution provide high coverage of the underlying amino acid residue locations, while accuracy of nodes is correlated with resolution. The nodes of graphs created from atomic resolution maps (higher than 1.6 Angstroms) provide greater than 99% residue coverage as well as 85% full atomic coverage with a mean of than 0.19 Angstrom root mean squared deviation (RMSD). Other graphs have a mean 84% residue coverage with less specificity of the nodes due to experimental noise and differences of density context at lower resolutions. This work may be generalized for transforming any 3D grid-based data format into non-linear, continuous, and differentiable format for the downstream geometric deep learning applications.
 
  Search related documents: 
                                Co phrase  search for related documents- absolute error and loss function: 1, 2
- absolute error and low resolution: 1, 2
- absolute error and mae mean absolute error: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73
- absolute error and mae mean absolute error metric: 1
 
                                Co phrase  search for related documents, hyperlinks ordered by date