Investigating Structural Biophysical Features for Antigen-Binding Fragment Crystallization via Machine Learning
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D4ME00187G.pdf
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Author(s)
Chattaraj, Krishna Gopal
Ferreira, Joana
Myerson, Allan S.
Trout, Bernhardt L.
Date Issued
February 28, 2025
Journal
Molecular Systems Design & Engineering
Publisher
Royal Society of Chemistry
Citation
Chattaraj, Krishna Gopal, Ferreira, Joana, Myerson, Allan S. and Trout, Bernhardt L. 2025. "Investigating Structural Biophysical Features for Antigen-Binding Fragment Crystallization via Machine Learning." Molecular Systems Design & Engineering, 10 (5).
Version
Final published version
Abstract
Antibody-based therapeutics continue to be an important pharmaceutical development modality. Crystallization of antibodies is important for structural characterization, but in addition has the potential for use as a separation method and for use as a dosage form. Nevertheless, bringing about controlled crystallization of an antibody remains a challenging task due to its large size, high degree of segmental flexibility, and the intricacy of all the occurring interactions (e.g., protein–protein interactions, protein–solvent interactions, etc.). Methods to predict important contact sites could help to develop such crystallization methods. However, limited data and understanding have hitherto not allowed the development of such robust methods. This study employs machine learning combined with in silico modelling of crystal structures using available experimental structures to identify the crucial physicochemical features necessary for successful antibody crystallization in an attempt to remedy that gap. The developed method can with good accuracy distinguish crystal-site residues from non-crystal-site residues. A set of 510 descriptors is utilized to characterize each residue, which is treated as a distinct data point. Moreover, new algorithms have been developed to design novel descriptors that improve the model's predictive capabilities. Fragment antigen-binding (Fab) regions are investigated due to the scarcity of full-length monoclonal antibodies (mAbs) crystal structures. The current findings show that the extreme gradient boosting (XGBoost) algorithm effectively identifies crystal site residues, as evidenced by an AUPRC value that is more than 3-fold higher than that of the baseline model. The top-ranked descriptors indicate that crystal-site residues are primarily characterized by solvent-exposed residues with high spatial aggregation propensity (SAP), signifying hydrophobic patches, and their immediate surface-exposed neighbors. Moreover, these high SAP residues are often surrounded by other solvent-exposed residues that are either polar, charged, or both. In contrast, residues not involved in crystal interfaces generally lack these essential features, though some might be excluded due to specific crystal lattice arrangements. Additionally, reducing the feature set from 510 to the top 15% in the XGBoost model yields similar performance while significantly simplifying the model.
MIT Department
Massachusetts Institute of Technology. Department of Chemical Engineering
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Creative Commons Attribution
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DOI of Published Version
https://doi.org/10.1039/D4ME00187G
