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A Nanobody‐on‐Quantum Dot Displacement Assay for Rapid and Sensitive Quantification of the Epidermal Growth Factor Receptor (EGFR)
Biosensing approaches that combine small, engineered antibodies (nanobodies) with nanoparticles are often complicated. Here, we show that nanobodies with different C‐terminal tags can be efficiently attached to a range of the most widely used biocompatible semiconductor quantum dots (QDs). Direct im...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9542526/ https://www.ncbi.nlm.nih.gov/pubmed/35759268 http://dx.doi.org/10.1002/anie.202207797 |
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author | Su, Ruifang Wu, Yu‐Tang Doulkeridou, Sofia Qiu, Xue Sørensen, Thomas Just Susumu, Kimihiro Medintz, Igor L. van Bergen en Henegouwen, Paul M. P. Hildebrandt, Niko |
author_facet | Su, Ruifang Wu, Yu‐Tang Doulkeridou, Sofia Qiu, Xue Sørensen, Thomas Just Susumu, Kimihiro Medintz, Igor L. van Bergen en Henegouwen, Paul M. P. Hildebrandt, Niko |
author_sort | Su, Ruifang |
collection | PubMed |
description | Biosensing approaches that combine small, engineered antibodies (nanobodies) with nanoparticles are often complicated. Here, we show that nanobodies with different C‐terminal tags can be efficiently attached to a range of the most widely used biocompatible semiconductor quantum dots (QDs). Direct implementation into simplified assay formats was demonstrated by designing a rapid and wash‐free mix‐and‐measure immunoassay for the epidermal growth factor receptor (EGFR). Terbium complex (Tb)‐labeled hexahistidine‐tagged nanobodies were specifically displaced from QD surfaces via EGFR‐nanobody binding, leading to an EGFR concentration‐dependent decrease of the Tb‐to‐QD Förster resonance energy transfer (FRET) signal. The detection limit of 80±20 pM (16±4 ng mL(−1)) was 3‐fold lower than the clinical cut‐off concentration for soluble EGFR and up to 10‐fold lower compared to conventional sandwich FRET assays that required a pair of different nanobodies. |
format | Online Article Text |
id | pubmed-9542526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95425262022-10-14 A Nanobody‐on‐Quantum Dot Displacement Assay for Rapid and Sensitive Quantification of the Epidermal Growth Factor Receptor (EGFR) Su, Ruifang Wu, Yu‐Tang Doulkeridou, Sofia Qiu, Xue Sørensen, Thomas Just Susumu, Kimihiro Medintz, Igor L. van Bergen en Henegouwen, Paul M. P. Hildebrandt, Niko Angew Chem Int Ed Engl Communications Biosensing approaches that combine small, engineered antibodies (nanobodies) with nanoparticles are often complicated. Here, we show that nanobodies with different C‐terminal tags can be efficiently attached to a range of the most widely used biocompatible semiconductor quantum dots (QDs). Direct implementation into simplified assay formats was demonstrated by designing a rapid and wash‐free mix‐and‐measure immunoassay for the epidermal growth factor receptor (EGFR). Terbium complex (Tb)‐labeled hexahistidine‐tagged nanobodies were specifically displaced from QD surfaces via EGFR‐nanobody binding, leading to an EGFR concentration‐dependent decrease of the Tb‐to‐QD Förster resonance energy transfer (FRET) signal. The detection limit of 80±20 pM (16±4 ng mL(−1)) was 3‐fold lower than the clinical cut‐off concentration for soluble EGFR and up to 10‐fold lower compared to conventional sandwich FRET assays that required a pair of different nanobodies. John Wiley and Sons Inc. 2022-07-08 2022-08-15 /pmc/articles/PMC9542526/ /pubmed/35759268 http://dx.doi.org/10.1002/anie.202207797 Text en © 2022 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH 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 | Communications Su, Ruifang Wu, Yu‐Tang Doulkeridou, Sofia Qiu, Xue Sørensen, Thomas Just Susumu, Kimihiro Medintz, Igor L. van Bergen en Henegouwen, Paul M. P. Hildebrandt, Niko A Nanobody‐on‐Quantum Dot Displacement Assay for Rapid and Sensitive Quantification of the Epidermal Growth Factor Receptor (EGFR) |
title | A Nanobody‐on‐Quantum Dot Displacement Assay for Rapid and Sensitive Quantification of the Epidermal Growth Factor Receptor (EGFR) |
title_full | A Nanobody‐on‐Quantum Dot Displacement Assay for Rapid and Sensitive Quantification of the Epidermal Growth Factor Receptor (EGFR) |
title_fullStr | A Nanobody‐on‐Quantum Dot Displacement Assay for Rapid and Sensitive Quantification of the Epidermal Growth Factor Receptor (EGFR) |
title_full_unstemmed | A Nanobody‐on‐Quantum Dot Displacement Assay for Rapid and Sensitive Quantification of the Epidermal Growth Factor Receptor (EGFR) |
title_short | A Nanobody‐on‐Quantum Dot Displacement Assay for Rapid and Sensitive Quantification of the Epidermal Growth Factor Receptor (EGFR) |
title_sort | nanobody‐on‐quantum dot displacement assay for rapid and sensitive quantification of the epidermal growth factor receptor (egfr) |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9542526/ https://www.ncbi.nlm.nih.gov/pubmed/35759268 http://dx.doi.org/10.1002/anie.202207797 |
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