A Comparative Assessment of Ranking Accuracies of Conventional and Machine-Learning-Based Scoring Functions for Protein-Ligand Binding Affinity Prediction

2012 ◽  
Vol 9 (5) ◽  
pp. 1301-1313 ◽  
Author(s):  
Hossam M. Ashtawy ◽  
Nihar R. Mahapatra
Keyword(s):  
Machine Learning ◽  
Ligand Binding ◽  
Binding Affinity ◽  
Comparative Assessment ◽  
Scoring Functions ◽  
Binding Affinity Prediction ◽  
Affinity Prediction

scholarly journals Persistent spectral–based machine learning (PerSpect ML) for protein-ligand binding affinity prediction

2021 ◽  
Vol 7 (19) ◽  
pp. eabc5329
Author(s):  
Zhenyu Meng ◽  
Kelin Xia
Keyword(s):  
Machine Learning ◽  
Data Analysis ◽  
Ligand Binding ◽  
Binding Affinity ◽  
Molecular Descriptors ◽  
Biological Data ◽  
Learning Models ◽  
Binding Affinity Prediction ◽  
Affinity Prediction ◽  
Spectral Models

Molecular descriptors are essential to not only quantitative structure-activity relationship (QSAR) models but also machine learning–based material, chemical, and biological data analysis. Here, we propose persistent spectral–based machine learning (PerSpect ML) models for drug design. Different from all previous spectral models, a filtration process is introduced to generate a sequence of spectral models at various different scales. PerSpect attributes are defined as the function of spectral variables over the filtration value. Molecular descriptors obtained from PerSpect attributes are combined with machine learning models for protein-ligand binding affinity prediction. Our results, for the three most commonly used databases including PDBbind-2007, PDBbind-2013, and PDBbind-2016, are better than all existing models, as far as we know. The proposed PerSpect theory provides a powerful feature engineering framework. PerSpect ML models demonstrate great potential to significantly improve the performance of learning models in molecular data analysis.

scholarly journals Learning from the ligand: using ligand-based features to improve binding affinity prediction

2019 ◽  
Author(s):  
Fergus Boyles ◽  
Charlotte M Deane ◽  
Garrett M Morris
Keyword(s):  
Machine Learning ◽  
Binding Affinity ◽  
Pearson Correlation ◽  
Scoring Function ◽  
Supplementary Information ◽  
Scoring Functions ◽  
Limited Information ◽  
Ligand Complex ◽  
Binding Affinity Prediction ◽  
Affinity Prediction

Abstract Motivation Machine learning scoring functions for protein–ligand binding affinity prediction have been found to consistently outperform classical scoring functions. Structure-based scoring functions for universal affinity prediction typically use features describing interactions derived from the protein–ligand complex, with limited information about the chemical or topological properties of the ligand itself. Results We demonstrate that the performance of machine learning scoring functions are consistently improved by the inclusion of diverse ligand-based features. For example, a Random Forest (RF) combining the features of RF-Score v3 with RDKit molecular descriptors achieved Pearson correlation coefficients of up to 0.836, 0.780 and 0.821 on the PDBbind 2007, 2013 and 2016 core sets, respectively, compared to 0.790, 0.746 and 0.814 when using the features of RF-Score v3 alone. Excluding proteins and/or ligands that are similar to those in the test sets from the training set has a significant effect on scoring function performance, but does not remove the predictive power of ligand-based features. Furthermore a RF using only ligand-based features is predictive at a level similar to classical scoring functions and it appears to be predicting the mean binding affinity of a ligand for its protein targets. Availability and implementation Data and code to reproduce all the results are freely available at http://opig.stats.ox.ac.uk/resources. Supplementary information Supplementary data are available at Bioinformatics online.

Extended connectivity interaction features: improving binding affinity prediction through chemical description

2020 ◽  
Author(s):  
Norberto Sánchez-Cruz ◽  
José L Medina-Franco ◽  
Jordi Mestres ◽  
Xavier Barril
Keyword(s):  
Machine Learning ◽  
Binding Affinity ◽  
Pearson Correlation ◽  
Correlation Coefficients ◽  
Supplementary Information ◽  
Scoring Functions ◽  
Binding Affinity Prediction ◽  
Affinity Prediction ◽  
Extended Connectivity ◽  
Chemical Description

Abstract Motivation Machine-learning scoring functions (SFs) have been found to outperform standard SFs for binding affinity prediction of protein–ligand complexes. A plethora of reports focus on the implementation of increasingly complex algorithms, while the chemical description of the system has not been fully exploited. Results Herein, we introduce Extended Connectivity Interaction Features (ECIF) to describe protein–ligand complexes and build machine-learning SFs with improved predictions of binding affinity. ECIF are a set of protein−ligand atom-type pair counts that take into account each atom’s connectivity to describe it and thus define the pair types. ECIF were used to build different machine-learning models to predict protein–ligand affinities (pKd/pKi). The models were evaluated in terms of ‘scoring power’ on the Comparative Assessment of Scoring Functions 2016. The best models built on ECIF achieved Pearson correlation coefficients of 0.857 when used on its own, and 0.866 when used in combination with ligand descriptors, demonstrating ECIF descriptive power. Availability and implementation Data and code to reproduce all the results are freely available at https://github.com/DIFACQUIM/ECIF. Contact [email protected] Supplementary information Supplementary data are available at Bioinformatics online.

Persistent spectral hypergraph based machine learning (PSH-ML) for protein-ligand binding affinity prediction

2021 ◽  
Author(s):  
Xiang Liu ◽  
Huitao Feng ◽  
Jie Wu ◽  
Kelin Xia
Keyword(s):  
Machine Learning ◽  
Ligand Binding ◽  
Binding Affinity ◽  
Molecular Descriptors ◽  
Biological Data ◽  
Learning Models ◽  
Filtration Process ◽  
Binding Affinity Prediction ◽  
Affinity Prediction ◽  
Machine Learning Models

Abstract Molecular descriptors are essential to not only quantitative structure activity/property relationship (QSAR/QSPR) models, but also machine learning based chemical and biological data analysis. In this paper, we propose persistent spectral hypergraph (PSH) based molecular descriptors or fingerprints for the first time. Our PSH-based molecular descriptors are used in the characterization of molecular structures and interactions, and further combined with machine learning models, in particular gradient boosting tree (GBT), for protein-ligand binding affinity prediction. Different from traditional molecular descriptors, which are usually based on molecular graph models, a hypergraph-based topological representation is proposed for protein–ligand interaction characterization. Moreover, a filtration process is introduced to generate a series of nested hypergraphs in different scales. For each of these hypergraphs, its eigen spectrum information can be obtained from the corresponding (Hodge) Laplacain matrix. PSH studies the persistence and variation of the eigen spectrum of the nested hypergraphs during the filtration process. Molecular descriptors or fingerprints can be generated from persistent attributes, which are statistical or combinatorial functions of PSH, and combined with machine learning models, in particular, GBT. We test our PSH-GBT model on three most commonly used datasets, including PDBbind-2007, PDBbind-2013 and PDBbind-2016. Our results, for all these databases, are better than all existing machine learning models with traditional molecular descriptors, as far as we know.

scholarly journals Learning from the Ligand: Using Ligand-Based Features to Improve Binding Affinity Prediction

2019 ◽  
Author(s):  
Fergus Boyles ◽  
Charlotte M Deane ◽  
Garrett Morris
Keyword(s):  
Machine Learning ◽  
Random Forest ◽  
Binding Affinity ◽  
Pearson Correlation ◽  
Scoring Function ◽  
Scoring Functions ◽  
Limited Information ◽  
Ligand Complex ◽  
Binding Affinity Prediction ◽  
Affinity Prediction

Machine learning scoring functions for protein-ligand binding affinity prediction have been found to consistently outperform classical scoring functions. Structure-based scoring functions for universal affinity prediction typically use features describing interactions derived from the protein-ligand complex, with limited information about the chemical or topological properties of the ligand itself. We demonstrate that the performance of machine learning scoring functions are consistently improved by the inclusion of diverse ligand-based features. For example, a Random Forest combining the features of RF-Score v3 with RDKit molecular descriptors achieved Pearson correlation coefficients of up to 0.831, 0.785, and 0.821 on the PDBbind 2007, 2013, and 2016 core sets respectively, compared to 0.790, 0.737, and 0.797 when using the features of RF-Score v3 alone. Excluding proteins and/or ligands that are similar to those in the test sets from the training set has a significant effect on scoring function performance, but does not remove the predictive power of ligand-based features. Furthermore a Random Forest using only ligand-based features is predictive at a level similar to classical scoring functions and it appears to be predicting the mean binding affinity of a ligand for its protein targets.<br>

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