Computational nanobody design using graph neural networks and Metropolis Monte Carlo sampling.

Abstract

Nanobodies are promising protein therapeutics due to their high-stability, low immunogenicity, and ease of production. However, experimental screening of high-affinity nanobodies and their post optimization remain costly and time-consuming due to the vast variant space. Here, we developed a computational approach that integrates graph neural networks (GNNs) with Monte Carlo Metropolis algorithm for nanobody design. We constructed a GNN model, AiPPA, to predict the protein-protein binding free energy (BFE) without requiring the complex structure, achieving a Pearson correlation of 0.62 on benchmark. We then combined AiPPA with Metropolis importance sampling to design low-BFE nanobodies from a non-affinity template. We applied this method to the antigen TL1A and generated two affinity nanobodies. This work establishes a physics-informed deep learning method for computational nanobody design, providing a novel development strategy for protein therapeutics.