Graph identification of proteins in tomograms (GRIP‐Tomo)

• Published in: Protein science Vol. 32; no. 1; pp. e4538 - n/a
• Main Authors: George, August, Kim, Doo Nam, Moser, Trevor, Gildea, Ian T., Evans, James E., Cheung, Margaret S.
• Format: Journal Article
• Language: English
• Published: Hoboken, USA John Wiley & Sons, Inc 01.01.2023; Wiley Subscription Services, Inc
• Subjects: Centroids; Data mining; Defects; dimensional reduction; Full‐length Paper; Full‐length Papers; graph theory; Graphs; Human bias; Humans; Mathematical morphology; multimeric structure; native structure; network theory; Order parameters; Pattern analysis; Proteins; Simulation; Topology; dimensional reduction; network theory; multimeric structure; graph theory; native structure
• ISSN: 0961-8368; 1469-896X; 1469-896X
• DOI: 10.1002/pro.4538

In this study, we present a method of pattern mining based on network theory that enables the identification of protein structures or complexes from synthetic volume densities, without the knowledge of predefined templates or human biases for refinement. We hypothesized that the topological connectivity of protein structures is invariant, and they are distinctive for the purpose of protein identification from distorted data presented in volume densities. Three‐dimensional densities of a protein or a complex from simulated tomographic volumes were transformed into mathematical graphs as observables. We systematically introduced data distortion or defects such as missing fullness of data, the tumbling effect, and the missing wedge effect into the simulated volumes, and varied the distance cutoffs in pixels to capture the varying connectivity between the density cluster centroids in the presence of defects. A similarity score between the graphs from the simulated volumes and the graphs transformed from the physical protein structures in point data was calculated by comparing their network theory order parameters including node degrees, betweenness centrality, and graph densities. By capturing the essential topological features defining the heterogeneous morphologies of a network, we were able to accurately identify proteins and homo‐multimeric complexes from 10 topologically distinctive samples without realistic noise added. Our approach empowers future developments of tomogram processing by providing pattern mining with interpretability, to enable the classification of single‐domain protein native topologies as well as distinct single‐domain proteins from multimeric complexes within noisy volumes.