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Machine-learning-based structural analysis of interactions between antibodies and antigens.
Zhang, Grace; Kuang, Xiaohan; Zhang, Yuhao; Liu, Yunchao; Su, Zhaoqian; Zhang, Tom; Wu, Yinghao.
Afiliação
  • Zhang G; Staples High School, 70 North Avenue, Westport, CT, 06880, USA.
  • Kuang X; Data Science Institute, Vanderbilt University, 1001 19th Ave S, Nashville, TN, 37212, USA.
  • Zhang Y; Data Science Institute, Vanderbilt University, 1001 19th Ave S, Nashville, TN, 37212, USA.
  • Liu Y; Department of Computer Science, Vanderbilt University, 1400 18th Ave S, Nashville, TN, 37212, USA.
  • Su Z; Data Science Institute, Vanderbilt University, 1001 19th Ave S, Nashville, TN, 37212, USA.
  • Zhang T; California Institute of Technology, 1200 East California Boulevard, Pasadena, CA, 91125, USA. Electronic address: txzhang@caltech.edu.
  • Wu Y; Department of Systems and Computational Biology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY, 10461, USA. Electronic address: yinghao.wu@einsteinmed.edu.
Biosystems ; 243: 105264, 2024 Sep.
Article em En | MEDLINE | ID: mdl-38964652
ABSTRACT
Computational analysis of paratope-epitope interactions between antibodies and their corresponding antigens can facilitate our understanding of the molecular mechanism underlying humoral immunity and boost the design of new therapeutics for many diseases. The recent breakthrough in artificial intelligence has made it possible to predict protein-protein interactions and model their structures. Unfortunately, detecting antigen-binding sites associated with a specific antibody is still a challenging problem. To tackle this challenge, we implemented a deep learning model to characterize interaction patterns between antibodies and their corresponding antigens. With high accuracy, our model can distinguish between antibody-antigen complexes and other types of protein-protein complexes. More intriguingly, we can identify antigens from other common protein binding regions with an accuracy of higher than 70% even if we only have the epitope information. This indicates that antigens have distinct features on their surface that antibodies can recognize. Additionally, our model was unable to predict the partnerships between antibodies and their particular antigens. This result suggests that one antigen may be targeted by more than one antibody and that antibodies may bind to previously unidentified proteins. Taken together, our results support the precision of antibody-antigen interactions while also suggesting positive future progress in the prediction of specific pairing.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aprendizado de Máquina / Anticorpos / Antígenos Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aprendizado de Máquina / Anticorpos / Antígenos Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article