Protein-protein interactions (PPIs) are pivotal in cellular processes, influencing a wide range of functions, from metabolism to immune responses. Despite the advancements in experimental techniques for PPI detection, their inherent limitations, such as high false-positive rates and significant resource demands, necessitate the development of computational approaches. This study presents a novel computational model named MFPIC (Multi-Feature Protein Interaction Classifier) for predicting PPIs, integrating enhanced sequence-based features, including a novel spaced conjoint triad (SCT) and amino acid pairwise distance (AAPD), with existing methods such as position-specific scoring matrices (PSSM) and AAindex-based features. The SCT captures complex sequence motifs by considering non-adjacent amino acid interactions, while AAPD provides critical spatial information about amino acid residues within protein sequences. The proposed model was evaluated across three benchmark datasets-Saccharomyces cerevisiae, Helicobacter pylori, and human proteins-demonstrating superior performance in comparison to state-of-the-art models. The results underscore the efficacy of integrating diverse and complementary features, achieving significant improvements in predictive accuracy, with the model achieving 95.90%, 99.33%, and 90.95% accuracy on the Saccharomyces cerevisiae, Helicobacter pylori, and human dataset, respectively. This approach not only enhances our understanding of PPI mechanisms but also offers valuable insights for the development of targeted therapeutic strategies.

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Journal Article

Authors

Göktepe YE

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