APIS: accurate prediction of hot spots in protein interfaces by combining protrusion index with solvent accessibility
Open Access
- 8 April 2010
- journal article
- research article
- Published by Springer Nature in BMC Bioinformatics
- Vol. 11 (1) , 174
Abstract
Background: It is well known that most of the binding free energy of protein interaction is contributed by a few key hot spot residues. These residues are crucial for understanding the function of proteins and studying their interactions. Experimental hot spots detection methods such as alanine scanning mutagenesis are not applicable on a large scale since they are time consuming and expensive. Therefore, reliable and efficient computational methods for identifying hot spots are greatly desired and urgently required. Results: In this work, we introduce an efficient approach that uses support vector machine (SVM) to predict hot spot residues in protein interfaces. We systematically investigate a wide variety of 62 features from a combination of protein sequence and structure information. Then, to remove redundant and irrelevant features and improve the prediction performance, feature selection is employed using the F-score method. Based on the selected features, nine individual-feature based predictors are developed to identify hot spots using SVMs. Furthermore, a new ensemble classifier, namely APIS (A combined model based on Protrusion Index and Solvent accessibility), is developed to further improve the prediction accuracy. The results on two benchmark datasets, ASEdb and BID, show that this proposed method yields significantly better prediction accuracy than those previously published in the literature. In addition, we also demonstrate the predictive power of our proposed method by modelling two protein complexes: the calmodulin/myosin light chain kinase complex and the heat shock locus gene products U and V complex, which indicate that our method can identify more hot spots in these two complexes compared with other state-of-the-art methods. Conclusion: We have developed an accurate prediction model for hot spot residues, given the structure of a protein complex. A major contribution of this study is to propose several new features based on the protrusion index of amino acid residues, which has been shown to significantly improve the prediction performance of hot spots. Moreover, we identify a compact and useful feature subset that has an important implication for identifying hot spot residues. Our results indicate that these features are more effective than the conventional evolutionary conservation, pairwise residue potentials and other traditional features considered previously, and that the combination of our and traditional features may support the creation of a discriminative feature set for efficient prediction of hot spot residues. The data and source code are available on web site http://home.ustc.edu.cn/~jfxia/hotspot.html.Keywords
This publication has 55 references indexed in Scilit:
- Prediction of hot spot residues at protein-protein interfaces by combining machine learning and energy-based methodsBMC Bioinformatics, 2009
- A feature-based approach to modeling protein–protein interaction hot spotsNucleic Acids Research, 2009
- ‘Double water exclusion’: a hypothesis refining the O-ring theory for the hot spots at protein interfacesBioinformatics, 2009
- Prediction of protein-protein binding site by using core interface residue and support vector machineBMC Bioinformatics, 2008
- The ConSurf-DB: pre-calculated evolutionary conservation profiles of protein structuresNucleic Acids Research, 2008
- KFC Server: interactive forecasting of protein interaction hot spotsNucleic Acids Research, 2008
- Uncovering signal transduction networks from high-throughput data by integer linear programmingNucleic Acids Research, 2008
- PSAIA – Protein Structure and Interaction AnalyzerBMC Structural Biology, 2008
- HotSprint: database of computational hot spots in protein interfacesNucleic Acids Research, 2007
- VMD: Visual molecular dynamicsJournal of Molecular Graphics, 1996