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Bioluminescent Antibodies for Point‐of‐Care Diagnostics

We introduce a general method to transform antibodies into ratiometric, bioluminescent sensor proteins for the no‐wash quantification of analytes. Our approach is based on the genetic fusion of antibody fragments to NanoLuc luciferase and SNAP‐tag, the latter being labeled with a synthetic fluoresce...

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Detalles Bibliográficos
Autores principales: Xue, Lin, Yu, Qiuliyang, Griss, Rudolf, Schena, Alberto, Johnsson, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5488172/
https://www.ncbi.nlm.nih.gov/pubmed/28510347
http://dx.doi.org/10.1002/anie.201702403
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author Xue, Lin
Yu, Qiuliyang
Griss, Rudolf
Schena, Alberto
Johnsson, Kai
author_facet Xue, Lin
Yu, Qiuliyang
Griss, Rudolf
Schena, Alberto
Johnsson, Kai
author_sort Xue, Lin
collection PubMed
description We introduce a general method to transform antibodies into ratiometric, bioluminescent sensor proteins for the no‐wash quantification of analytes. Our approach is based on the genetic fusion of antibody fragments to NanoLuc luciferase and SNAP‐tag, the latter being labeled with a synthetic fluorescent competitor of the antigen. Binding of the antigen, here synthetic drugs, by the sensor displaces the tethered fluorescent competitor from the antibody and disrupts bioluminescent resonance energy transfer (BRET) between the luciferase and fluorophore. The semisynthetic sensors display a tunable response range (submicromolar to submillimolar) and large dynamic range (ΔR (max)>500 %), and they permit the quantification of analytes through spotting of the samples onto paper followed by analysis with a digital camera.
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spelling pubmed-54881722017-07-24 Bioluminescent Antibodies for Point‐of‐Care Diagnostics Xue, Lin Yu, Qiuliyang Griss, Rudolf Schena, Alberto Johnsson, Kai Angew Chem Int Ed Engl Communications We introduce a general method to transform antibodies into ratiometric, bioluminescent sensor proteins for the no‐wash quantification of analytes. Our approach is based on the genetic fusion of antibody fragments to NanoLuc luciferase and SNAP‐tag, the latter being labeled with a synthetic fluorescent competitor of the antigen. Binding of the antigen, here synthetic drugs, by the sensor displaces the tethered fluorescent competitor from the antibody and disrupts bioluminescent resonance energy transfer (BRET) between the luciferase and fluorophore. The semisynthetic sensors display a tunable response range (submicromolar to submillimolar) and large dynamic range (ΔR (max)>500 %), and they permit the quantification of analytes through spotting of the samples onto paper followed by analysis with a digital camera. John Wiley and Sons Inc. 2017-05-16 2017-06-12 /pmc/articles/PMC5488172/ /pubmed/28510347 http://dx.doi.org/10.1002/anie.201702403 Text en © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Communications
Xue, Lin
Yu, Qiuliyang
Griss, Rudolf
Schena, Alberto
Johnsson, Kai
Bioluminescent Antibodies for Point‐of‐Care Diagnostics
title Bioluminescent Antibodies for Point‐of‐Care Diagnostics
title_full Bioluminescent Antibodies for Point‐of‐Care Diagnostics
title_fullStr Bioluminescent Antibodies for Point‐of‐Care Diagnostics
title_full_unstemmed Bioluminescent Antibodies for Point‐of‐Care Diagnostics
title_short Bioluminescent Antibodies for Point‐of‐Care Diagnostics
title_sort bioluminescent antibodies for point‐of‐care diagnostics
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5488172/
https://www.ncbi.nlm.nih.gov/pubmed/28510347
http://dx.doi.org/10.1002/anie.201702403
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