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Light-guided intrabodies for on-demand in situ target recognition in human cells
Due to their high stability and specificity in living cells, fluorescently labeled nanobodies are perfect probes for visualizing intracellular targets at an endogenous level. However, intrabodies bind unrestrainedly and hence may interfere with the target protein function. Here, we report a strategy...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8872839/ https://www.ncbi.nlm.nih.gov/pubmed/35342543 http://dx.doi.org/10.1039/d1sc01331a |
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author | Joest, Eike F. Winter, Christian Wesalo, Joshua S. Deiters, Alexander Tampé, Robert |
author_facet | Joest, Eike F. Winter, Christian Wesalo, Joshua S. Deiters, Alexander Tampé, Robert |
author_sort | Joest, Eike F. |
collection | PubMed |
description | Due to their high stability and specificity in living cells, fluorescently labeled nanobodies are perfect probes for visualizing intracellular targets at an endogenous level. However, intrabodies bind unrestrainedly and hence may interfere with the target protein function. Here, we report a strategy to prevent premature binding through the development of photo-conditional intrabodies. Using genetic code expansion, we introduce photocaged amino acids within the nanobody-binding interface, which, after photo-activation, show instantaneous binding of target proteins with high spatiotemporal precision inside living cells. Due to the highly stable binding, light-guided intrabodies offer a versatile platform for downstream imaging and regulation of target proteins. |
format | Online Article Text |
id | pubmed-8872839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-88728392022-03-24 Light-guided intrabodies for on-demand in situ target recognition in human cells Joest, Eike F. Winter, Christian Wesalo, Joshua S. Deiters, Alexander Tampé, Robert Chem Sci Chemistry Due to their high stability and specificity in living cells, fluorescently labeled nanobodies are perfect probes for visualizing intracellular targets at an endogenous level. However, intrabodies bind unrestrainedly and hence may interfere with the target protein function. Here, we report a strategy to prevent premature binding through the development of photo-conditional intrabodies. Using genetic code expansion, we introduce photocaged amino acids within the nanobody-binding interface, which, after photo-activation, show instantaneous binding of target proteins with high spatiotemporal precision inside living cells. Due to the highly stable binding, light-guided intrabodies offer a versatile platform for downstream imaging and regulation of target proteins. The Royal Society of Chemistry 2021-04-08 /pmc/articles/PMC8872839/ /pubmed/35342543 http://dx.doi.org/10.1039/d1sc01331a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Joest, Eike F. Winter, Christian Wesalo, Joshua S. Deiters, Alexander Tampé, Robert Light-guided intrabodies for on-demand in situ target recognition in human cells |
title | Light-guided intrabodies for on-demand in situ target recognition in human cells |
title_full | Light-guided intrabodies for on-demand in situ target recognition in human cells |
title_fullStr | Light-guided intrabodies for on-demand in situ target recognition in human cells |
title_full_unstemmed | Light-guided intrabodies for on-demand in situ target recognition in human cells |
title_short | Light-guided intrabodies for on-demand in situ target recognition in human cells |
title_sort | light-guided intrabodies for on-demand in situ target recognition in human cells |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8872839/ https://www.ncbi.nlm.nih.gov/pubmed/35342543 http://dx.doi.org/10.1039/d1sc01331a |
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