Data-driven analyses of human antibody variable domain germlines: pairings, sequences and structural features

The Observed Antibody Space provides the most abundant collection of annotated paired antibody variable domain sequences, thus offering a unique platform for the systematic investigation of the factors governing the pairing of antibody heavy and light chains. By examining a range of characteristics, including amino acid conservation, structural features, charge distribution, and interface residue identity, we challenge the prevailing assumption that pairing is random. Our findings indicate that specific physicochemical properties of single amino acid residues may influence the compatibility and affinity of heavy and light chain combinations. Further structural analyses based on antibody Fv fragments deposited in the Protein Data Bank (PDB) provide insights into the underlying structural features driving these pairing preferences, including a novel definition for the residues constituting the V<sub>H</sub>-V<sub>L</sub> interface, based on a collection of over 3500 structures. These results have significant implications for understanding antibody assembly and may guide the rational design of therapeutic antibodies with desired properties. Moreover, we provide a complete description and reference characterizing the various human germlines.

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Publication Details

Journal
mAbs
Published
2025-05-25
DOI
https://doi.org/10.1080/19420862.2025.2507950
Citations
7
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
Field-Weighted Citation Impact
9.52

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article

Data-driven analyses of human antibody variable domain germlines: pairings, sequences and structural features

Alexander Bujotzek, Klaus Roman Liedl, Jakob Gamper, Guy Georges et al.
7 citations
mAbs
Monoclonal and Polyclonal Antibodies Research
9.52
article

Data-driven analyses of human antibody variable domain germlines: pairings, sequences and structural features

Alexander Bujotzek, Klaus Roman Liedl, Jakob Gamper, Guy Georges, Clarissa A. Seidler, Vera A. Spanke
article en
7 citations

Abstract

The Observed Antibody Space provides the most abundant collection of annotated paired antibody variable domain sequences, thus offering a unique platform for the systematic investigation of the factors governing the pairing of antibody heavy and light chains. By examining a range of characteristics, including amino acid conservation, structural features, charge distribution, and interface residue identity, we challenge the prevailing assumption that pairing is random. Our findings indicate that specific physicochemical properties of single amino acid residues may influence the compatibility and affinity of heavy and light chain combinations. Further structural analyses based on antibody Fv fragments deposited in the Protein Data Bank (PDB) provide insights into the underlying structural features driving these pairing preferences, including a novel definition for the residues constituting the V<sub>H</sub>-V<sub>L</sub> interface, based on a collection of over 3500 structures. These results have significant implications for understanding antibody assembly and may guide the rational design of therapeutic antibodies with desired properties. Moreover, we provide a complete description and reference characterizing the various human germlines.

mAbsVol. 17(1)
Roche (Switzerland) (CH), Universität Innsbruck (AT), Roche Pharma AG (Germany) (DE)
Austrian Science Fund
Zero hunger
Openalex Percentile: Top 2%
Monoclonal and Polyclonal Antibodies Research
9.52
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Data-driven analyses of human antibody variable domain germlines: pairings, sequences and structural features — Alexander Bujotzek, Klaus Roman Liedl, et al. · mAbs (2025) | TGRS Research Map | TGRS