pengxingang / TEIM

TEIM: TCR-Epitope Interaction Modeling

TEIM: TCR-Epitope Interaction Modeling

This repository contains the codes for the paper TEIM: Characterizing the interaction conformation between T-cell receptors and epitopes with deep learning published in Nature Machine Intelligence.

TEIM (TCR-Epitope Interaction Modeling) is a deep learning-based model to predict the TCR-epitope interactions, including two submodels TEIM-Res (TEIM at Residue level) and TEIM-Samp (TEIM at Sequence level).

Both models only takes the primary sequences of CDR3βs and the epitopes as input. TEIM-Res predicts the distances and the contact probabilities between all residue pairs of CDR3βs and epitopes. TEIM-Seq predicts whether the CDR3βs and epitopes can bind to each other.

Dependency

0. Install Python>=3.8 and Anaconda.
1. Install basic packages using:

   # [Optional] Create a new environment and activate it
   conda create -n teim python=3.8
   conda activate teim
   
   # Install Pytorch packages (for CUDA 11.3)
   conda install pytorch==1.10.1 cudatoolkit=11.3 -c pytorch -c conda-forge
   # Install other packages
   pip install -r requirements.txt
   

   Note: Change the Pytorch version to be compatible with your CUDA version. Besides, since the Pytorch Lightning version we used is 1.6.4, the compatible Pytorch version is $>=1.8,<=1.11$ (see here).
2. Install ANARCI for CDR3 numbering.

   conda install -c bioconda anarci
   

We also provided a docker file to facilitate the installation of environment. You can build the docker by runing

docker build -t teim:v1 .

Inference

Predict the residue-level interactions of TCR-epitope pairs

1. Put your input TCR-epitope sequence pairs in the inputs/inputs.csv file. The TCRs are represented by their CDR3β sequences and the epitopes are represented by their sequences in the following format:

   cdr3	epitope
   CASAPGLAGGRPEQYF	LLFGYPVYV
   CASRGAAGGRPQYF	MLWGYLQYV
   CASRPGLAGGRAEQYF	FTDSSVWA

2. Run

   python scripts/inference_res.py
   

3. The predicted distance matrices and contact site matrices are in the outputs directory:

   • The predicted distance matrix and contact matrix are in the files names as dist_<cdr3>_<epitope>.csv and site_<cdr3>_<epitope>.csv, respectively.
   • The rows and columns of the matrices represent the CDR3βs and epitopes, respectively.
   • The values in the distance matrix stand for the distances of residue pairs (unit: angstrom) and the values in the contact matrix stand for the predicted contact scores (probabilities) of residue pairs (range from 0 to 1).

Predict the seqence-level interactions of TCR-epitope pairs

1. Put your input TCR-epitope sequence pairs in the inputs/inputs_bd.csv file. The format is the same as inputs/inputs.csv (residue-level input file).
2. Run

   python scripts/inference_seq.py
   

3. The predicted sequence-level binding scores are in the outputs/sequence_level_binding.csv. The binding column in the file represent the predicted sequence-level binding scores (probabilities) of the TCR-epitope pair.

Training

Please refer to the directory train_teim.

Citation

@article{Peng2023,
  doi = {10.1038/s42256-023-00634-4},
  url = {https://doi.org/10.1038/s42256-023-00634-4},
  year = {2023},
  month = mar,
  publisher = {Springer Science and Business Media {LLC}},
  volume = {5},
  number = {4},
  pages = {395--407},
  author = {Xingang Peng and Yipin Lei and Peiyuan Feng and Lemei Jia and Jianzhu Ma and Dan Zhao and Jianyang Zeng},
  title = {Characterizing the interaction conformation between T-cell receptors and epitopes with deep learning},
  journal = {Nature Machine Intelligence}
}

Contact

If you have any questions, please contact us at [e-mail]