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Anti-coronavirus peptides (ACVPs) represent a relatively novel approach of inhibiting the adsorption and fusion of the virus with human cells. Several peptide-based inhibitors showed promise as potential therapeutic drug candidates. However, identifying such peptides in laboratory experiments is both costly and time consuming. Therefore, there is growing interest in using computational methods to predict ACVPs. Here, we describe a model for the prediction of ACVPs that is based on the combination of feature engineering (FE) optimization and deep representation learning. FEOpti-ACVP was pre-trained using two feature extraction frameworks. At the next step, several machine learning approaches were tested in to construct the final algorithm. The final version of FEOpti-ACVP outperformed existing methods used for ACVPs prediction and it has the potential to become a valuable tool in ACVP drug design. A user-friendly webserver of FEOpti-ACVP can be accessed at http://servers.aibiochem.net/soft/FEOpti-ACVP/., (© The Author(s) 2024. Published by Oxford University Press.)

Interleukin-10 (IL-10) has anti-inflammatory properties and is a crucial cytokine in regulating immunity. The identification of IL-10 through wet laboratory experiments is costly and time-intensive. Therefore, a new IL-10-induced peptide recognition method, IL10-Stack, was introduced in this research, which was based on unified deep representation learning and a stacking algorithm. Two approaches were employed to extract features from peptide sequences: Amino Acid Index (AAindex) and sequence-based unified representation (UniRep). After feature fusion and optimized feature selection, we selected a 1900-dimensional UniRep feature vector and constructed the IL10-Stack model using stacking. IL10-Stack exhibited excellent performance in IL-10-induced peptide recognition (accuracy (ACC) = 0.910, Matthews correlation coefficient (MCC) = 0.820). Relative to the existing methods, IL-10Pred and ILeukin10Pred, the approach increased in ACC by 12.1% and 2.4%, respectively. The IL10-Stack method can identify IL-10-induced peptides, which aids in the development of immunosuppressive drugs. [ABSTRACT FROM AUTHOR]