ANTIPASTI: Interpretable prediction of antibody binding affinity exploiting normal modes and deep learning

The high binding affinity of antibodies toward their cognate targets is key to eliciting effective immune responses, as well as to the use of antibodies as research and therapeutic tools. Here, we propose ANTIPASTI, a convolutional neural network model that achieves state-of-the-art performance in the prediction of antibody binding affinity using as input a representation of antibody-antigen structures in terms of normal mode correlation maps derived from elastic network models. This representation captures not only structural features but energetic patterns of local and global residue fluctuations. The learnt representations are interpretable: they reveal similarities of binding patterns among antibodies targeting the same antigen type, and can be used to quantify the importance of antibody regions contributing to binding affinity. Our results show the importance of the antigen imprint in the normal mode landscape, and the dominance of cooperative effects and long-range correlations between antibody regions to determine binding affinity.

Authors

Institutions

Publication Details

Journal
Structure
Published
2024-10-25
DOI
https://doi.org/10.1016/j.str.2024.10.001
Citations
11
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
Field-Weighted Citation Impact
4.45

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

ANTIPASTI: Interpretable prediction of antibody binding affinity exploiting normal modes and deep learning

Kevin Michalewicz, Barbara Bravi, Mauricio Barahona
11 citations
Structure
Monoclonal and Polyclonal Antibodies Research
4.45
article

ANTIPASTI: Interpretable prediction of antibody binding affinity exploiting normal modes and deep learning

Kevin Michalewicz, Barbara Bravi, Mauricio Barahona
article en
11 citations

Abstract

The high binding affinity of antibodies toward their cognate targets is key to eliciting effective immune responses, as well as to the use of antibodies as research and therapeutic tools. Here, we propose ANTIPASTI, a convolutional neural network model that achieves state-of-the-art performance in the prediction of antibody binding affinity using as input a representation of antibody-antigen structures in terms of normal mode correlation maps derived from elastic network models. This representation captures not only structural features but energetic patterns of local and global residue fluctuations. The learnt representations are interpretable: they reveal similarities of binding patterns among antibodies targeting the same antigen type, and can be used to quantify the importance of antibody regions contributing to binding affinity. Our results show the importance of the antigen imprint in the normal mode landscape, and the dominance of cooperative effects and long-range correlations between antibody regions to determine binding affinity.

StructureVol. 32(12)
Imperial College London (GB)
Imperial College London, Engineering and Physical Sciences Research Council
Openalex Percentile: Top 5%
Monoclonal and Polyclonal Antibodies Research
4.45
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

ANTIPASTI: Interpretable prediction of antibody binding affinity exploiting normal modes and deep learning — Kevin Michalewicz, Barbara Bravi, et al. · Structure (2024) | TGRS Research Map | TGRS