Antibody-enabled structural biology and AI-driven antibody design

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Authors: Khuram U. Ashraf, Satchal K. Erramilli
Cited by: 0
References: 69

Abstract

Membrane proteins govern essential cellular processes, including ion transport, signal transduction, and molecular recognition, and collectively represent more than half of all current therapeutic targets. Yet their structural characterization remains challenging due to intrinsic instability, amphipathic surfaces, and conformational heterogeneity. Over the past decade, antibody-based approaches, spanning full-length immunoglobulins, antigen-binding fragments (Fabs), nanobodies, and engineered scaffolds such as designed ankyrin repeat proteins (DARPins), have transformed structural biology by stabilizing dynamic states, augmenting molecular weight for cryo-electron microscopy (cryo-EM), and enabling visualization of previously inaccessible complexes. In parallel, advances in artificial intelligence and machine learning have begun to enhance predictive modeling, accelerate structure determination, and guide rational design of protein-ligand and antibody-antigen interactions. This review examines how antibody engineering and AI-driven computation together are reshaping the landscape of structural biology and therapeutic discovery.

Fields of Study & Subjects

Monoclonal and Polyclonal Antibodies Research Protein Structure and Dynamics Enzyme Structure and Function

Publication details

Journal / source
Frontiers in Pharmacology
Volume
17
Pages
1773629–1773629
Publication date
27 February 2026
Language
EN