Cell-Based Immunization Combined with Single-Round Cell Panning Enables Discovery of PSMA-Targeting Nanobodies from Phage Display Libraries

There is a strong need for nanobodies that target novel cancer-associated antigens to advance radioligand imaging and antibody-based therapeutics. In this study, we investigated whether non-targeted llama immunization using tumor cells, combined with non-targeted phage-display panning of human cell lines, could yield nanobodies specific to Prostate-Specific Membrane Antigen (PSMA). Nanobody selection using both classical three-round PSMA negative-positive panning and single-round panning of cell lines (positive or negative) for PSMA showed clear enrichment for PSMA binders in both strategies. Using shRNA knockdown, flow cytometry, cell-ELISA, immunohistochemistry and structural modeling and docking, we confirmed the PSMA-targeting of selected nanobodies. Two distinct epitopes were predicted to be bound by nanobodies PSMANb9 and A7 (JVZ-007), and this was corroborated by epitope competition assays. These findings support the feasibility of non-targeted immunization and panning strategies for isolating antigen-targeting cancer nanobodies.

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Publication Details

Journal
Biomolecules
Published
2026-02-14
DOI
https://doi.org/10.3390/biom16020307
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
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article

Cell-Based Immunization Combined with Single-Round Cell Panning Enables Discovery of PSMA-Targeting Nanobodies from Phage Display Libraries

S Erkens, Job van Riet, Guido Jenster, Joke Veldhoven-Zweistra et al.
Biomolecules
Monoclonal and Polyclonal Antibodies Research
article

Cell-Based Immunization Combined with Single-Round Cell Panning Enables Discovery of PSMA-Targeting Nanobodies from Phage Display Libraries

S Erkens, Job van Riet, Guido Jenster, Joke Veldhoven-Zweistra, Mirella Vredenbregt-van den Berg, Raheleh Tooyserkani, Maarten A. Ligtenberg, Janne Leivo, Khadijeh Ahmadi, Patrick Chames, Rick Jansen, Eric M. J. Bindels, Chris H. Bangma, Anton M. F. Kalsbeek, Soudabeh Kavousipour, Tong Yang, Wytske M. van Weerden
article en

Abstract

There is a strong need for nanobodies that target novel cancer-associated antigens to advance radioligand imaging and antibody-based therapeutics. In this study, we investigated whether non-targeted llama immunization using tumor cells, combined with non-targeted phage-display panning of human cell lines, could yield nanobodies specific to Prostate-Specific Membrane Antigen (PSMA). Nanobody selection using both classical three-round PSMA negative-positive panning and single-round panning of cell lines (positive or negative) for PSMA showed clear enrichment for PSMA binders in both strategies. Using shRNA knockdown, flow cytometry, cell-ELISA, immunohistochemistry and structural modeling and docking, we confirmed the PSMA-targeting of selected nanobodies. Two distinct epitopes were predicted to be bound by nanobodies PSMANb9 and A7 (JVZ-007), and this was corroborated by epitope competition assays. These findings support the feasibility of non-targeted immunization and panning strategies for isolating antigen-targeting cancer nanobodies.

BiomoleculesVol. 16(2)
HOGENT University of Applied Sciences and Arts (BE), Centre National de la Recherche Scientifique (FR), Inserm (FR), University of Turku (FI), Ghent University Hospital (BE), Erasmus MC (NL), Ghent University (BE), Hormozgan University of Medical Sciences (IR), Centre de Recherche en Cancérologie de Marseille (FR), Erasmus MC Cancer Institute (NL), Institut Paoli-Calmettes (FR), Bushehr University of Medical Sciences (IR)
Good health and well-being
Openalex Percentile: Top 55%
Monoclonal and Polyclonal Antibodies Research
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