most citedInverse folding for antibody sequence design using deep learning

21 citations · 43 across the 5 of their papers we have counts for

collaborators

5 papers

q-bio.BM2024★ 3 cited

Assessing interaction recovery of predicted protein-ligand poses

David Errington, Constantin Schneider, Cédric Bouysset +1

The field of protein-ligand pose prediction has seen significant advances in recent years, with machine learning-based methods now being commonly used in lieu of classical docking…

q-bio.BM2024★ 3 cited

ABodyBuilder3: Improved and scalable antibody structure predictions

Henry Kenlay, Frédéric A. Dreyer, Daniel Cutting +2

Accurate prediction of antibody structure is a central task in the design and development of monoclonal antibodies, notably to understand both their developability and their bindin…

q-bio.BM2024★ 10 cited

De novo antibody design with SE(3) diffusion

Daniel Cutting, Frédéric A. Dreyer, David Errington +2

We introduce IgDiff, an antibody variable domain diffusion model based on a general protein backbone diffusion framework which was extended to handle multiple chains. Assessing the…

q-bio.BM2024★ 6 cited

Large scale paired antibody language models

Henry Kenlay, Frédéric A. Dreyer, Aleksandr Kovaltsuk +3

Antibodies are proteins produced by the immune system that can identify and neutralise a wide variety of antigens with high specificity and affinity, and constitute the most succes…

q-bio.BM2023★ 21 cited

Inverse folding for antibody sequence design using deep learning

Frédéric A. Dreyer, Daniel Cutting, Constantin Schneider +2

We consider the problem of antibody sequence design given 3D structural information. Building on previous work, we propose a fine-tuned inverse folding model that is specifically o…