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CHIMERA-Bench: A Benchmark Dataset for Epitope-Specific Antibody Design

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abstract

Computational antibody design has seen rapid methodological progress, with dozens of deep generative methods proposed in the past three years, yet the field lacks a standardized benchmark for fair comparison and model development. These methods are evaluated on different SAbDab snapshots, non-overlapping test sets, and incompatible metrics, and the literature fragments the design problem into numerous sub-tasks with no common definition. We introduce CHIMERA-Bench: (CDR Modeling with Epitope-guided Redesign), a unified benchmark built around a single canonical task: epitope-conditioned CDR sequence-structure co-design. CHIMERA-Bench provides three components. The first is a curated, deduplicated dataset of 2,922 antibody-antigen complexes with epitope and paratope annotations. The second is a set of three biologically motivated splits that test generalization to unseen epitopes, unseen antigen folds, and prospective temporal targets. The third is a comprehensive evaluation protocol with five metric groups, including novel epitope-specificity measures. We benchmark eleven methods spanning six generative paradigms and report results across all splits. CHIMERA-Bench is the largest dataset of its kind for the antibody design problem, allowing the community to develop and test novel methods and evaluate their generalizability.

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cs.CL 1

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2026 1

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  • EpiBench: Can LLMs Understand Epitopes for Antibody Drug Discovery? cs.CL · 2026-08-06 · conditional · none · ref 1 · internal anchor

    A new closed-book, sequence-only benchmark, EpiBench, measures epitope reasoning in LLMs and finds them near chance on residue-level localization and escape assessment, with only coarse region-level signal.