Related Experiment Video
Updated: Feb 20, 2026

PAR-CliP - A Method to Identify Transcriptome-wide the Binding Sites of RNA Binding Proteins
Published on: July 2, 2010
Paraplume: A fast and accurate antibody paratope prediction method provides insights into repertoire-scale binding
Gabriel Athènes1,2, Adam Woolfe2, Thierry Mora1
1Laboratoire de physique de l'École Normale Supérieure, CNRS, PSL University, Sorbonne Université, and Université de Paris, Paris, France.
Abstract:
The specific region of an antibody responsible for binding to an antigen, known as the paratope, is essential for immune recognition. Accurate identification of this small yet critical region can accelerate the development of therapeutic antibodies. Determining paratope locations typically relies on modeling the antibody structure, which is computationally intensive and difficult to scale across large antibody repertoires. We introduce Paraplume, a sequence-based paratope prediction method that leverages embeddings from protein language models (PLMs), without the need for structural input and achieves superior performance across multiple benchmarks compared to current methods. In addition, reweighting PLM embeddings using Paraplume predictions yields more informative sequence representations, improving downstream tasks such as binder classification and epitope binning. Applied to large antibody repertoires, Paraplume reveals that antigen-specific somatic hypermutations are associated with larger paratopes, suggesting a potential mechanism for affinity enhancement. Our findings position PLM-based paratope prediction as a powerful, scalable alternative to structure-dependent approaches, opening new avenues for understanding antibody evolution.

