Predicting lncRNA-protein interactions using a hybrid deep learning model with dinucleotide-codon fusion feature encoding.

Long non-coding RNAs (lncRNAs) play crucial roles in numerous biological processes and are involved in complex human diseases through interactions with proteins. Accurate identification of lncRNA-protein interactions (LPI) can help elucidate the functional mechanisms of lncRNAs and provide scientific insights into the molecular mechanisms underlying related diseases. While many sequence-based methods have been developed to predict LPIs, efficiently extracting and effectively integrating potential feature information that reflects functional attributes from lncRNA and protein sequences remains a significant challenge. This paper proposes a Dinucleotide-Codon Fusion Feature encoding (DNCFF) and constructs an LPI prediction model based on deep learning, termed LPI-DNCFF. The Dual Nucleotide Visual Fusion Feature encoding (DNVFF) incorporates positional information of single nucleotides with subsequent nucleotide connections, while Codon Fusion Feature encoding (CFF) considers the specificity, molecular weight, and physicochemical properties of each amino acid. These encoding methods encapsulate rich and intuitive sequence information in limited encoding dimensions. The model comprehensively predicts LPIs by integrating global, local, and structural features, and inputs them into BiLSTM and attention layers to form a hybrid deep learning model. Experimental results demonstrate that LPI-DNCFF effectively predicts LPIs. The BiLSTM layer and attention mechanism can learn long-term dependencies and identify weighted key features, enhancing model performance. Compared to one-hot encoding, DNCFF more efficiently and thoroughly extracts potential sequence features. Compared to other existing methods, LPI-DNCFF achieved the best performance on the RPI1847 and ATH948 datasets, with MCC values of approximately 97.84% and 84.58%, respectively, outperforming the state-of-the-art method by about 1.44% and 3.48%.