An Effective Approach for Clustering InhA Molecular Dynamics Trajectory Using Substrate-Binding Cavity Features
| Autor: | Duncan D. Ruiz, Renata De Paris, Christian Vahl Quevedo, Osmar Norberto de Souza |
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| Rok vydání: | 2015 |
| Předmět: |
Computer science
Protein Conformation Science Crystal structure Molecular Dynamics Simulation Bioinformatics Molecular Docking Simulation Molecular dynamics Protein structure Bacterial Proteins Cluster Analysis Binding site Cluster analysis chemistry.chemical_classification Multidisciplinary Binding Sites biology Drug discovery Active site NAD Complete linkage Medoid Hierarchical clustering Enzyme chemistry Docking (molecular) Searching the conformational space for docking biology.protein Medicine Biological system Oxidoreductases Algorithms Research Article |
| Zdroj: | PLoS ONE PLoS ONE, Vol 10, Iss 7, p e0133172 (2015) |
| ISSN: | 1932-6203 |
| Popis: | Protein receptor conformations, obtained from molecular dynamics (MD) simulations, have become a promising treatment of its explicit flexibility in molecular docking experiments applied to drug discovery and development. However, incorporating the entire ensemble of MD conformations in docking experiments to screen large candidate compound libraries is currently an unfeasible task. Clustering algorithms have been widely used as a means to reduce such ensembles to a manageable size. Most studies investigate different algorithms using pairwise Root-Mean Square Deviation (RMSD) values for all, or part of the MD conformations. Nevertheless, the RMSD only may not be the most appropriate gauge to cluster conformations when the target receptor has a plastic active site, since they are influenced by changes that occur on other parts of the structure. Hence, we have applied two partitioning methods (k-means and k-medoids) and four agglomerative hierarchical methods (Complete linkage, Ward’s, Unweighted Pair Group Method and Weighted Pair Group Method) to analyze and compare the quality of partitions between a data set composed of properties from an enzyme receptor substrate-binding cavity and two data sets created using different RMSD approaches. Ensembles of representative MD conformations were generated by selecting a medoid of each group from all partitions analyzed. We investigated the performance of our new method for evaluating binding conformation of drug candidates to the InhA enzyme, which were performed by cross-docking experiments between a 20 ns MD trajectory and 20 different ligands. Statistical analyses showed that the novel ensemble, which is represented by only 0.48% of the MD conformations, was able to reproduce 75% of all dynamic behaviors within the binding cavity for the docking experiments performed. Moreover, this new approach not only outperforms the other two RMSD-clustering solutions, but it also shows to be a promising strategy to distill biologically relevant information from MD trajectories, especially for docking purposes. |
| Databáze: | OpenAIRE |
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