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NKp46‐specific single domain antibodies enable facile engineering of various potent NK cell engager formats
Herein, we describe the generation of potent NK cell engagers (NKCEs) based on single domain antibodies (sdAbs) specific for NKp46 harboring the humanized Fab version of Cetuximab for tumor targeting. After immunization of camelids, a plethora of different VHH domains were retrieved by yeast surface...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9951198/ https://www.ncbi.nlm.nih.gov/pubmed/36775946 http://dx.doi.org/10.1002/pro.4593 |
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author | Lipinski, Britta Arras, Paul Pekar, Lukas Klewinghaus, Daniel Boje, Ammelie Svea Krah, Simon Zimmermann, Jasmin Klausz, Katja Peipp, Matthias Siegmund, Vanessa Evers, Andreas Zielonka, Stefan |
author_facet | Lipinski, Britta Arras, Paul Pekar, Lukas Klewinghaus, Daniel Boje, Ammelie Svea Krah, Simon Zimmermann, Jasmin Klausz, Katja Peipp, Matthias Siegmund, Vanessa Evers, Andreas Zielonka, Stefan |
author_sort | Lipinski, Britta |
collection | PubMed |
description | Herein, we describe the generation of potent NK cell engagers (NKCEs) based on single domain antibodies (sdAbs) specific for NKp46 harboring the humanized Fab version of Cetuximab for tumor targeting. After immunization of camelids, a plethora of different VHH domains were retrieved by yeast surface display. Upon reformatting into Fc effector‐silenced NKCEs targeting NKp46 and EGFR in a strictly monovalent fashion, the resulting bispecific antibodies elicited potent NK cell‐mediated killing of EGFR‐overexpressing tumor cells with potencies (EC(50)killing) in the picomolar range. This was further augmented via co‐engagement of Fcγ receptor IIIa (FcγRIIIa). Importantly, NKp46‐specific sdAbs enabled the construction of various NKCE formats with different geometries and valencies which displayed favorable biophysical and biochemical properties without further optimization. By this means, killing capacities were further improved significantly. Hence, NKp46‐specific sdAbs are versatile building blocks for the construction of different NKCE formats. |
format | Online Article Text |
id | pubmed-9951198 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99511982023-02-25 NKp46‐specific single domain antibodies enable facile engineering of various potent NK cell engager formats Lipinski, Britta Arras, Paul Pekar, Lukas Klewinghaus, Daniel Boje, Ammelie Svea Krah, Simon Zimmermann, Jasmin Klausz, Katja Peipp, Matthias Siegmund, Vanessa Evers, Andreas Zielonka, Stefan Protein Sci Full‐length Papers Herein, we describe the generation of potent NK cell engagers (NKCEs) based on single domain antibodies (sdAbs) specific for NKp46 harboring the humanized Fab version of Cetuximab for tumor targeting. After immunization of camelids, a plethora of different VHH domains were retrieved by yeast surface display. Upon reformatting into Fc effector‐silenced NKCEs targeting NKp46 and EGFR in a strictly monovalent fashion, the resulting bispecific antibodies elicited potent NK cell‐mediated killing of EGFR‐overexpressing tumor cells with potencies (EC(50)killing) in the picomolar range. This was further augmented via co‐engagement of Fcγ receptor IIIa (FcγRIIIa). Importantly, NKp46‐specific sdAbs enabled the construction of various NKCE formats with different geometries and valencies which displayed favorable biophysical and biochemical properties without further optimization. By this means, killing capacities were further improved significantly. Hence, NKp46‐specific sdAbs are versatile building blocks for the construction of different NKCE formats. John Wiley & Sons, Inc. 2023-02-24 /pmc/articles/PMC9951198/ /pubmed/36775946 http://dx.doi.org/10.1002/pro.4593 Text en © 2023 The Authors. Protein Science published by Wiley Periodicals LLC on behalf of The Protein Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full‐length Papers Lipinski, Britta Arras, Paul Pekar, Lukas Klewinghaus, Daniel Boje, Ammelie Svea Krah, Simon Zimmermann, Jasmin Klausz, Katja Peipp, Matthias Siegmund, Vanessa Evers, Andreas Zielonka, Stefan NKp46‐specific single domain antibodies enable facile engineering of various potent NK cell engager formats |
title |
NKp46‐specific single domain antibodies enable facile engineering of various potent NK cell engager formats |
title_full |
NKp46‐specific single domain antibodies enable facile engineering of various potent NK cell engager formats |
title_fullStr |
NKp46‐specific single domain antibodies enable facile engineering of various potent NK cell engager formats |
title_full_unstemmed |
NKp46‐specific single domain antibodies enable facile engineering of various potent NK cell engager formats |
title_short |
NKp46‐specific single domain antibodies enable facile engineering of various potent NK cell engager formats |
title_sort | nkp46‐specific single domain antibodies enable facile engineering of various potent nk cell engager formats |
topic | Full‐length Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9951198/ https://www.ncbi.nlm.nih.gov/pubmed/36775946 http://dx.doi.org/10.1002/pro.4593 |
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