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DG-Affinity: predicting antigen-antibody affinity with language models from sequences.

Ye Yuan1, Qushuo Chen2, Jun Mao2

  • 1Institute of Image Processing and Pattern Recognition, Shanghai Jiao Tong University, and Key Laboratory of System Control and Information Processing, Ministry of Education of China, Shanghai, 200240, China. yuanye_auto@sjtu.edu.cn.

BMC Bioinformatics
|November 14, 2023
PubMed
Summary
This summary is machine-generated.

A new method, DG-Affinity, accurately predicts antigen-antibody affinity using only sequences and deep learning. This advances antibody design for therapeutic development.

Keywords:
AffinityAntibody–antigen interactionDeep learningSequence embedding

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Area of Science:

  • Biotechnology
  • Immunology
  • Computational Biology

Background:

  • Antibody-mediated immunity is vital for human defense.
  • Bioengineered antibody-derived drugs show promise for cancer and autoimmune diseases.
  • Accurate prediction of antigen-antibody affinity is critical for antibody development.

Purpose of the Study:

  • To introduce DG-Affinity, a novel sequence-based method for predicting antigen-antibody affinity.
  • To demonstrate the efficacy of DG-Affinity without requiring structural information.

Main Methods:

  • Utilized deep neural networks and pre-trained language models to transform antibody and antigen sequences into embedding vectors.
  • Employed a ConvNeXt framework with a regression task to predict affinity from concatenated embeddings.

Main Results:

  • DG-Affinity accurately predicts antigen-antibody affinity from sequences alone.
  • Achieved a Pearson's correlation coefficient exceeding 0.65 on an independent test dataset.
  • Outperformed existing structure-based and sequence-based prediction methods.

Conclusions:

  • DG-Affinity demonstrates superior performance compared to baseline methods.
  • The method can significantly advance antibody design and development.
  • DG-Affinity is accessible via a free web server for ease of use.