Challenges in antibody structure prediction

MAbs. 2023 Jan-Dec;15(1):2175319. doi: 10.1080/19420862.2023.2175319.

Abstract

Advances in structural biology and the exponential increase in the amount of high-quality experimental structural data available in the Protein Data Bank has motivated numerous studies to tackle the grand challenge of predicting protein structures. In 2020 AlphaFold2 revolutionized the field using a combination of artificial intelligence and the evolutionary information contained in multiple sequence alignments. Antibodies are one of the most important classes of biotherapeutic proteins. Accurate structure models are a prerequisite to advance biophysical property predictions and consequently antibody design. Specialized tools used to predict antibody structures based on different principles have profited from current advances in protein structure prediction based on artificial intelligence. Here, we emphasize the importance of reliable protein structure models and highlight the enormous advances in the field, but we also aim to increase awareness that protein structure models, and in particular antibody models, may suffer from structural inaccuracies, namely incorrect cis-amide bonds, wrong stereochemistry or clashes. We show that these inaccuracies affect biophysical property predictions such as surface hydrophobicity. Thus, we stress the importance of carefully reviewing protein structure models before investing further computing power and setting up experiments. To facilitate the assessment of model quality, we provide a tool "TopModel" to validate structure models.

Keywords: Antibodies; antibody structure; biophysical surface properties; protein structure prediction; structural inaccuracies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies
  • Artificial Intelligence*
  • Computational Biology
  • Databases, Protein
  • Protein Conformation
  • Proteins* / chemistry

Substances

  • Proteins
  • Antibodies

Grants and funding

This work was supported by the Austrian Science Fund (FWF) [P34518]. This work was supported by the Austrian Academy of sciences APART-MINT postdoctoral fellowship to M.L.F.Q.