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Many proteins form complexes to carry out their functions, making protein-protein interactions (PPIs) essential for an organism's survival. Most PPIs are stabilized by numerous weak noncovalent chemical forces. The physical shape of the interfaces determines the way two proteins interact. Many globular proteins have closely-matching shapes on their surfaces, which form a large number of weak bonds. Additionally, many PPIs occur between two helices or between a surface cleft and a...
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An organism can have thousands of different proteins, and these proteins must cooperate to ensure the health of an organism. Proteins bind to other proteins and form complexes to carry out their functions. Many proteins interact with multiple other proteins creating a complex network of protein interactions.
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Groups of proteins may form a complex where each protein in this complex has a different role in the overall execution of the complex’s function. Often some of the proteins in the complex can be replaced by a closely related variant to give a complex that contains many of the same components yet is functionally distinct.
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DeepHVI: A multimodal deep learning framework for predicting human-virus protein-protein interactions using protein

Xindi Wang1,2,3, Junyu Luo3, Xiyang Cai3

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This study introduces a deep learning framework to predict human-virus protein interactions, aiding in understanding viral infections and developing public health strategies against emerging diseases.

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Area of Science:

  • Virology
  • Computational Biology
  • Immunology

Background:

  • Understanding human-virus protein-protein interactions is crucial for deciphering viral pathogenesis, immune responses, and disease spread.
  • Existing methods for identifying these interactions are often limited in scope or efficiency.

Purpose of the Study:

  • To develop a novel multimodal deep learning framework for systematic prediction of human-virus protein-protein interactions.
  • To enhance the accuracy and efficiency of identifying biologically relevant protein partnerships.

Main Methods:

  • Integration of high-confidence experimental datasets with a multimodal deep learning approach.
  • Utilizing complementary tasks: binary classification for interaction prediction and conditional sequence generation.
  • Leveraging protein language models and multimodal fusion techniques.

Main Results:

  • The framework demonstrated improved accuracy in predicting biologically relevant human-virus protein interactions.
  • Application to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) identified novel candidate interactions, including those not present in the training data.
  • Several predicted interactions were corroborated by independent studies.

Conclusions:

  • The developed deep learning framework offers a powerful tool for rapid, cost-effective discovery of protein interactions critical for public health.
  • Predictions provide valuable insights into potential therapeutic targets for antiviral drugs and vaccines, contributing to pandemic preparedness.
  • This approach facilitates the design of novel interventions against emerging infectious diseases.