MEN: leveraging explainable multimodal encoding network for precision prediction of CYP450 inhibitors.

Journal: Scientific reports
Published Date:

Abstract

Drug-drug interactions (DDIs) present serious risks in clinical settings, especially for patients who are prescribed multiple medications. A major factor contributing to these interactions is the inhibition of cytochrome P450 (CYP450) enzymes, which are vital for drug metabolism. As a result, reliably identifying compounds that may inhibit CYP450 enzymes is a key step in drug development. However, existing machine learning (ML) methods often fall short in terms of prediction accuracy and biological interpretability. To address this challenge, we introduce a Multimodal Encoder Network (MEN) aimed at improving the prediction of CYP450 inhibitors. This model combines three types of molecular data (chemical fingerprints, molecular graphs, and protein sequences) by applying specialized encoders tailored to each format. Specifically, the Fingerprint Encoder Network (FEN) processes molecular fingerprints, the Graph Encoder Network (GEN) extracts structural features from graph-based representations, and the Protein Encoder Network (PEN) captures sequential patterns from protein sequences. By integrating these diverse data types, MEN can extract complementary information that enhances predictive performance. The encoded outputs from FEN, GEN, and PEN are fused to build a comprehensive feature representation. An explainable AI (XAI) module is incorporated into the model to support biological interpretation, using visualization techniques such as heatmaps. The model was trained and validated using two datasets: chemical structures in SMILES format from PubChem and protein sequences of five CYP450 isoforms (1A2, 2C9, 2C19, 2D6, and 3A4) obtained from the Protein Data Bank (PDB). MEN achieved an average accuracy of 93.7% across all isoforms. The individual encoders performed with accuracies of 80.8% (FEN), 82.3% (GEN), and 81.5% (PEN). Additional performance results include an AUC of 98.5%, sensitivity of 95.9%, specificity of 97.2%, precision of 80.6%, F1-score of 83.4%, and a Matthews correlation coefficient (MCC) of 88.2%. All data and code are available at https://github.com/GracedAbena/MEN-Leveraging-Explainable-Multimodal-Encoding-Network .

Authors

  • Abena Achiaa Atwereboannah
    School of Computer Science and Engineering, University of Electronic Science and Technology, Chengdu, People's Republic of China.
  • Wei-Ping Wu
    UESTC.
  • Mugahed A Al-Antari
    Department of Computer Science and Engineering, College of Software, Kyung Hee University, 1732, Deogyeong-daero, Giheung-gu, Yongin-si, Gyeonggi-do 17104 Republic of Korea.
  • Sophyani B Yussif
    School of Computer Science and Engineering, University of Electronic Science and Technology, Chengdu, People's Republic of China.
  • Chukwuebuka J Ejiyi
    School of Information and Software Engineering, University of Electronic Science and Technology of China, Sichuan, PR China.
  • Edwin K Tenagyei
    School of Engineering and Built Environment, Griffith University, Brisbane, QLD, 4111, Australia.
  • Grace-Mercure B Kissanga
    School of Life Science and Technology and Center for Informational Biology, University of Electronic Science and Technology of China, Chengdu, 610054, People's Republic of China.
  • Gyarteng S A Emmanuel
    School of Information and Communication Engineering, University of Electronic Science and Technology, Chengdu, People's Republic of China.
  • Yeong Hyeon Gu
    Department of Artificial Intelligence and Data Science, Sejong University, Seoul, Korea.
  • Emmanuel Ahene
    Department of Computer Science, Kwame Nkrumah University of Science and Technology Kumasi, Kumasi, Ghana.