CASLR is proposed, an antibody CDR-aware slot late-interaction retriever that encodes antigens with ESM-2, encodes antibodies with IgBert, constrains antibody-side latent slots to complementarity-determining regions (CDRs), and scores local slot compatibility instead of single-vector global similarity.
Abstract
Antigen-specific antibody retrieval aims to rank candidate antibodies for a target antigen, providing an early virtual-screening step before structural modeling or experimental validation. Existing sequence-based antibody-antigen interaction studies often formulate the problem as pairwise binding prediction, and random or non-clustered evaluations can over-estimate generalization when related antigens appear across training and test data. We study a strict antigen-cluster out-of-distribution (OOD) retrieval setting in which test antigens come from sequence clusters unseen during training. This setting is difficult because binding is driven by local epitope-CDR complementarity, while available databases mainly contain observed positive complexes and lack reliable negative labels for unlabeled candidates. We propose Ab-CASLR, an antibody CDR-aware slot late-interaction retriever that encodes antigens with ESM-2, encodes antibodies with IgBert, constrains antibody-side latent slots to complementarity-determining regions (CDRs), and scores local slot compatibility instead of single-vector global similarity. On a strict OOD benchmark with 849 antigen queries and 869 candidate antibodies, the model achieves 7.42% Hits@10, outperforming k-mer homology transfer at 5.53% Hits@10 and yielding 6.28-fold enrichment over exact random screening at K = 10. Ablations and diagnostics show that CDR-constrained antibody slots remain diverse, whereas antigen-side latent slots collapse into similar summaries. These results support CDR-aware local antibody representation as a useful inductive bias for early binder recovery under strict OOD evaluation, while antigen-side epitope grounding remains unresolved.
AAMFM, an Antigen-specific Antibody Multimodal Foundation Model that learns unified representations of antibody sequences and structures conditioned on antigen context, achieves state-of-the-art performance in functional antibody design, revealing its potential for antigen-specific antibody engineering.
Xiaoliang Shi, Zichen Wang, Runze Ma et al.· 0 citations
AbICL is proposed, an ICL framework for antigen-specific antibody affinity ranking that combines a pretrained structural encoder with a context ranking head and is trained with an episodic meta-training strategy that enables the model to leverage support demonstrations for test-time adaptation without gradient updates.
Zhiyuan Chen, Jing Hu, Junzhe Wang et al.· 0 citations
Local-Frame 3D Rotary Position Encoding (LF3DRoPE), which expresses inter-residue displacements in backbone-defined local frames and injects them directly into rotary attention, preserves continuous directional geometry while ensuring invariance to global $\mathrm{SE}(3)$ transformations.
Chuanliu Fan, Nan Yu, Junjie Wu et al.· 0 citations
The most recent methods substantially outperformed earlier ones, producing medium-or-better top-ranked models for approximately half of post-cutoff Fv complexes without templates or experimental restraints, and performing similarly on antigens with or without a close pre-cutoff homolog.
Minjae Park, Roman Nett, Brian M. Petersen et al.· bioRxiv· 0 citations
SAASBench provides a framework for evaluating the model's ability to estimate the specificity of a candidate antibody in relevant settings, indicating that strong performance on traditional affinity benchmarks does not automatically translate into reliable antibody specificity estimation in proteome-derived settings.
Dmitriy Umerenkov, Ivan Poddiakov· Proceedings of the 32nd ACM...· 0 citations