Skip to content
Open access

Mimic antibodies: leveraging ligand mimicry for epitope-targeted antibody discovery

Aug 2026 · mAbs · Vol 18 · 2 citations · 32 references
Medicine

TL;DR

The concept of mimic antibodies–antibodies that recapitulate the binding mode of a target’s cognate ligand is investigated and established as a promising strategy for rational antibody selection, engineering, and design, with broad implications for therapeutic antibody development and drug discovery.

Abstract

ABSTRACT Antibodies are renowned for their ability to bind diverse targets with high affinity and specificity, yet identifying binders with predefined epitope specificity remains a major challenge. In this study, we investigate the concept of mimic antibodies–antibodies that recapitulate the binding mode of a target’s cognate ligand. Through a systematic analysis of the Protein Data Bank (PDB), we show that such mimicry is widespread and arises through diverse structural mechanisms, such as single-loop, multi-loop and scattered interaction mimicry. These findings indicate that protein interfaces impose strong constraints on binding, leading to convergent interaction solutions that can be independently discovered by antibodies. Building on these findings, we developed a ligand-guided strategy to mine immune repertoire data by selecting antibodies whose predicted binding interfaces mimic the interaction motif of a cognate ligand. Applied to the interaction between interleukin-18 (IL-18) and its receptor alpha (IL-18RA), mimicry-guided screening of a 20,000-sequence repertoire yielded 31 candidates, 11 of which (35% hit rate) bound the IL-18RA D3 domain, with eight reaching sub-nanomolar affinities that surpass the cognate ligand. Our findings establish mimic antibodies as a promising strategy for rational antibody selection, engineering, and design, with broad implications for therapeutic antibody development and drug discovery.

Read PDF

Similar papers

Open access Sep 2026

Discovery and engineering of bispecific TCR-mimic antibodies targeting peptide–HLA complex

An integrated platform for generating human antibodies that mimic T-cell receptors and recognize peptide-HLA complexes with high specificity and affinity is developed, demonstrating superior performance compared to competitors’ TCRm antibodies.

Jennifer Watkins-Yoon, Wei-Cheng Lu, E. Petrunak et al. · 0 citations
Open access Sep 2026

Sequence and structural determinants of efficacious de novo chimaeric antigen receptors

This framework synthesizes generative protein design workflows to screen 1,758 newly designed protein binders targeting BCMA, CD19 and CD22 for efficacy in scalable protein-binding, T-cell activation and in vivo killing assays, and develops computational and experimental heuristics to overcome limitations.

Arthur Chow, Ho-Yin Chu, Ruo-Fan Li et al. · 2 citations
#protein folding Open access Aug 2026

DyAb: sequence-based antibody design and property prediction in a low-data regime

DyAb is a pair-wise representation built on top of a pre-trained protein language model that achieves a Spearman rank correlation of up to 0.85 on binding affinity prediction across monoclonal antibodies targeting three different antigens.

J. Lin, Jennifer L. Hofmann, A. Leaver-Fay et al. · 0 citations
Aug 2026

Structure-Guided CDR3 Insertion Enables Affinity Maturation of Naive Single-Domain Antibodies against Small-Molecule Haptens.

A "structure-guided directed modification" strategy was developed that focuses on conformational tuning rather than simple side-chain replacement to overcome the structural and energetic barriers inherent in hapten recognition and provide a practical and efficient computational framework for assisting the rapid evoluti...

Zeng-Lin Yang, Guo-Qiang Li, Yuanyuan Ge et al. · 0 citations
Open access Sep 2026

Specificity-driven protein binder design with Odin-Multi

Odin-Multi is presented, a binder design framework that optimises a shared binder sequence against several complexes simultaneously, applying attractive objectives to on-targets and repulsive objectives to off-targets, and widens the range of binding behaviours accessible to computational design.

Valentas Brasas, C. R. Christensen, Kasper H. Björnsson et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.