Site-directed multivalent conjugation of antibodies to ubiquitinated payloads

Antibody conjugates are the foundation of a wide range of diagnostic and therapeutic applications. Although many antibody-conjugation techniques are robust and efficient, obtaining homogeneous multimeric conjugation products remains challenging. Here we report a modular and versatile technique for the site-directed multivalent conjugation of antibodies via the small-protein ubiquitin. Specifically, multiple ubiquitin fusions with antibodies, antibody fragments, nanobodies, peptides or small molecules such as fluorescent dyes can be conjugated to antibodies and nanobodies within 30 min. The technique, which we named 'ubi-tagging', allowed us to efficiently generate a bispecific T-cell engager as well as nanobodies conjugated to dendritic-cell-targeted antigens that led to potent T-cell responses. Using both recombinant ubi-tagged proteins and synthetic ubiquitin derivatives allows for the iterative, site-directed and multivalent conjugation of antibodies and nanobodies to a plethora of molecular moieties.

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Publication Details

Journal
Nature Biomedical Engineering
Published
2025-04-09
DOI
https://doi.org/10.1038/s41551-024-01342-z
Citations
5
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
Field-Weighted Citation Impact
6.80

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article

Site-directed multivalent conjugation of antibodies to ubiquitinated payloads

Martijn Verdoes, Marjolein Sluijter, Ian Derksen, Douwe J. Dijkstra et al.
5 citations
Nature Biomedical Engineering
Monoclonal and Polyclonal Antibodies Research
6.80
article

Site-directed multivalent conjugation of antibodies to ubiquitinated payloads

Martijn Verdoes, Marjolein Sluijter, Ian Derksen, Douwe J. Dijkstra, Angela F. El Hebieshy, Andrea Rodgers Furones, Felix L. Fennemann, Kim E. de Roode, Paul W.H.I. Parren, Zacharias Wijfjes, Cami Talavera Ormeño, Sandra Heskamp, Carl Gustav Figdor, Bjorn R. van Doodewaerd, Jim Middelburg, Leendert Adrianus Trouw, Bas van der Woning, Ferenc A. Scheeren, Hans de Haard, Thorbald van Hall, Gerbrand J. van der Heden van Noort, Floris J. van Dalen, Camille M. Le Gall, Johan M. S. van der Schoot, Huib Ovaa
article en
5 citations

Abstract

Antibody conjugates are the foundation of a wide range of diagnostic and therapeutic applications. Although many antibody-conjugation techniques are robust and efficient, obtaining homogeneous multimeric conjugation products remains challenging. Here we report a modular and versatile technique for the site-directed multivalent conjugation of antibodies via the small-protein ubiquitin. Specifically, multiple ubiquitin fusions with antibodies, antibody fragments, nanobodies, peptides or small molecules such as fluorescent dyes can be conjugated to antibodies and nanobodies within 30 min. The technique, which we named 'ubi-tagging', allowed us to efficiently generate a bispecific T-cell engager as well as nanobodies conjugated to dendritic-cell-targeted antigens that led to potent T-cell responses. Using both recombinant ubi-tagged proteins and synthetic ubiquitin derivatives allows for the iterative, site-directed and multivalent conjugation of antibodies and nanobodies to a plethora of molecular moieties.

Nature Biomedical EngineeringVol. 9(7)
Radboud University Nijmegen (NL), Leiden University Medical Center (NL), Radboud University Medical Center (NL), Nijmegen Institute for Scientist Practitioners in Addiction (NL), Tagworks Pharmaceuticals (Netherlands) (NL), Argenx (Belgium) (BE)
Nederlandse Organisatie voor Wetenschappelijk Onderzoek, Leids Universitair Medisch Centrum
Openalex Percentile: Top 3%
Monoclonal and Polyclonal Antibodies Research
6.80
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