Antibody-Antigen Docking and Design via Hierarchical Equivariant
Refinement
- URL: http://arxiv.org/abs/2207.06616v1
- Date: Thu, 14 Jul 2022 02:13:25 GMT
- Title: Antibody-Antigen Docking and Design via Hierarchical Equivariant
Refinement
- Abstract summary: We propose a new model called Hierarchical Equivariant Refinement Network (HERN) for paratope docking and design.
During docking, HERN employs a hierarchical message passing network to predict atomic forces and use them to refine a binding complex in an iterative, equivariant manner.
Our results show that HERN significantly outperforms prior state-of-the-art on paratope docking and design benchmarks.
- Score: 38.637412590671865
- License: http://arxiv.org/licenses/nonexclusive-distrib/1.0/
- Abstract: Computational antibody design seeks to automatically create an antibody that
binds to an antigen. The binding affinity is governed by the 3D binding
interface where antibody residues (paratope) closely interact with antigen
residues (epitope). Thus, predicting 3D paratope-epitope complex (docking) is
the key to finding the best paratope. In this paper, we propose a new model
called Hierarchical Equivariant Refinement Network (HERN) for paratope docking
and design. During docking, HERN employs a hierarchical message passing network
to predict atomic forces and use them to refine a binding complex in an
iterative, equivariant manner. During generation, its autoregressive decoder
progressively docks generated paratopes and builds a geometric representation
of the binding interface to guide the next residue choice. Our results show
that HERN significantly outperforms prior state-of-the-art on paratope docking
and design benchmarks.
Related papers
- Hyper-Fold: Exploring the Expressive Limit of Sequence-Geometry Learning for Proteins via Hypergraph Modeling [55.36837305276515]
We show that the complete bilinear operator over content-geometry outer products--the sufficient statistic of all second-order interactions--is the expressive ceiling.<n>We then introduce Hyper-Fold, a rank-K separable convolutional backbone approaching this ceiling at message-passing cost.
arXiv Detail & Related papers (2026-08-29T11:43:25Z) - Inter-Residue Geometry Attention for Antibody-Specific Epitope Prediction [8.509019866126222]
Local-Frame 3D Rotary Position.<n>EPEP aims to identify which antigen residues are recognized by a given antibody, a task that depends on the three-dimensional complementarity between CDRs and the antigen surface.<n>We propose Local-Frame 3D Rotary Position.<n>EPEP, which expresses inter-residue displacements in backbone-defined local frames and injects them directly into rotary attention.
arXiv Detail & Related papers (2026-08-02T08:48:07Z) - AgForce Enables Antigen-conditioned Generative Antibody Design [3.2018287682779003]
We propose a novel encoder-decoder architecture called AgForce.<n>It uses a graph neural network (GNN) as the encoder and specialized decoders for sequence-structure co-design.<n>It achieves the best binding quality and sequence recovery simultaneously on the CHIMERA-Bench dataset.
arXiv Detail & Related papers (2026-05-20T18:16:52Z) - AbFlow : End-to-end Paratope-Centric Antibody Design by Interaction Enhanced Flow Matching [41.128304772190454]
AbFlow is a flow-matching framework that leverages optimal transport to design full-atom antibodies end-to-end.<n>It produces superior antigen-antibody complexes, especially at the contact interface, and markedly improves the binding affinity of generated antibodies.
arXiv Detail & Related papers (2026-02-06T07:47:59Z) - Antibody Design and Optimization with Multi-scale Equivariant Graph Diffusion Models for Accurate Complex Antigen Binding [13.315597171727095]
We propose textbfAbMEGD, an end-to-end framework for antibody sequence and structure co-design.<n>AbMEGD combines atomic-level geometric features with residue-level embeddings, capturing local atomic details and global sequence-structure interactions.<n>Experiments using the SAbDab database demonstrate a 10.13% increase in amino acid recovery, 3.32% rise in improvement percentage, and a 0.062AA reduction in root mean square deviation.
arXiv Detail & Related papers (2025-06-26T02:45:38Z) - Towards More Accurate Full-Atom Antibody Co-Design [44.06939390661133]
Co-design represents a critical frontier in drug development, where accurate prediction of structure of complementarity-determining regions is essential for targeting specific equivariants.
Despite recent advances in graph neural networks for antibody design, current approaches often fall short in capturing the intricate interactions that govern antibody-antigen recognition and binding specificity.
We present Igformer, a novel end-to-end framework that addresses these limitations through personalized antibody-antigen binding interfaces.
arXiv Detail & Related papers (2025-02-11T13:33:28Z) - Relation-Aware Equivariant Graph Networks for Epitope-Unknown Antibody Design and Specificity Optimization [61.06622479173572]
We propose a novel Relation-Aware Design (RAAD) framework, which models antigen-antibody interactions for co-designing sequences and structures of antigen-specific CDRs.
Furthermore, we propose a new evaluation metric to better measure antibody specificity and develop a contrasting specificity-enhancing constraint to optimize the specificity of antibodies.
arXiv Detail & Related papers (2024-12-14T03:00:44Z) - Decoupled Sequence and Structure Generation for Realistic Antibody Design [45.72237864940556]
A dominant paradigm is to train a model to jointly generate the antibody sequence and the structure as a candidate.
We propose an antibody sequence-structure decoupling (ASSD) framework, which separates sequence generation and structure prediction.
ASSD shows improved performance in various antibody design experiments, while the composition-based objective successfully mitigates token repetition of non-autoregressive models.
arXiv Detail & Related papers (2024-02-08T13:02:05Z) - A Hierarchical Training Paradigm for Antibody Structure-sequence
Co-design [54.30457372514873]
We propose a hierarchical training paradigm (HTP) for the antibody sequence-structure co-design.
HTP consists of four levels of training stages, each corresponding to a specific protein modality.
Empirical experiments show that HTP sets the new state-of-the-art performance in the co-design problem.
arXiv Detail & Related papers (2023-10-30T02:39:15Z) - Spatial-Temporal Graph Enhanced DETR Towards Multi-Frame 3D Object Detection [54.041049052843604]
We present STEMD, a novel end-to-end framework that enhances the DETR-like paradigm for multi-frame 3D object detection.
First, to model the inter-object spatial interaction and complex temporal dependencies, we introduce the spatial-temporal graph attention network.
Finally, it poses a challenge for the network to distinguish between the positive query and other highly similar queries that are not the best match.
arXiv Detail & Related papers (2023-07-01T13:53:14Z) - AbODE: Ab Initio Antibody Design using Conjoined ODEs [8.523238510909955]
We develop a new generative model AbODE that extends graph PDEs to accommodate both contextual information and external interactions.
We unravel fundamental connections between AbODE and temporal networks as well as graph-matching networks.
arXiv Detail & Related papers (2023-05-31T14:40:47Z) - End-to-End Full-Atom Antibody Design [28.199522831859998]
There are two major defects in current learning-based methods, making them suboptimal or resource-intensive.
We propose dynamic Multi-channel Equivariant grAph Network (dyMEAN), an end-to-end full-atom model for E(3) antibody design.
Both 1D sequences and 3D structures are updated via an adaptive multi-channel encoder that is able to process protein residues of variable sizes when considering full atoms.
Experiments on CDR-H3 design, complex structure prediction, and affinity optimization demonstrate the superiority of our end-to-end framework and full-atom modeling.
arXiv Detail & Related papers (2023-02-01T03:13:19Z) - xTrimoABFold: De novo Antibody Structure Prediction without MSA [77.47606749555686]
We develop a novel model named xTrimoABFold to predict antibody structure from antibody sequence.
The model was trained end-to-end on the antibody structures in PDB by minimizing the ensemble loss of domain-specific focal loss on CDR and the frame-aligned point loss.
arXiv Detail & Related papers (2022-11-30T09:26:08Z) - Incorporating Pre-training Paradigm for Antibody Sequence-Structure
Co-design [134.65287929316673]
Deep learning-based computational antibody design has attracted popular attention since it automatically mines the antibody patterns from data that could be complementary to human experiences.
The computational methods heavily rely on high-quality antibody structure data, which is quite limited.
Fortunately, there exists a large amount of sequence data of antibodies that can help model the CDR and alleviate the reliance on structure data.
arXiv Detail & Related papers (2022-10-26T15:31:36Z) - Conditional Antibody Design as 3D Equivariant Graph Translation [28.199522831859998]
We propose Multi-channel Equivariant Attention Network (MEAN) to co-design 1D sequences and 3D structures of CDRs.
Our method significantly surpasses state-of-the-art models in sequence and structure modeling, antigen-binding CDR design, and binding affinity optimization.
arXiv Detail & Related papers (2022-08-12T01:00:59Z) - Simple End-to-end Deep Learning Model for CDR-H3 Loop Structure
Prediction [0.0]
We present an end-to-end model to predict CDR H3 loop structure, that performs on par with state-of-the-art methods.
We also raise an issue with a commonly used RosettaAntibody benchmark that leads to data leaks.
arXiv Detail & Related papers (2021-11-20T18:55:09Z) - Unsupervised Geodesic-preserved Generative Adversarial Networks for
Unconstrained 3D Pose Transfer [84.04540436494011]
We present an unsupervised approach to conduct the pose transfer between any arbitrated given 3D meshes.
Specifically, a novel Intrinsic-Extrinsic Preserved Generative Adrative Network (IEP-GAN) is presented for both intrinsic (i.e., shape) and extrinsic (i.e., pose) information preservation.
Our proposed model produces better results and is substantially more efficient compared to recent state-of-the-art methods.
arXiv Detail & Related papers (2021-08-17T09:08:21Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.