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LITESEC-T3SS - Light-controlled protein delivery into eukaryotic cells with high spatial and temporal resolution
Many bacteria employ a type III secretion system (T3SS) injectisome to translocate proteins into eukaryotic host cells. Although the T3SS can efficiently export heterologous cargo proteins, a lack of target cell specificity currently limits its application in biotechnology and healthcare. In this st...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7221075/ https://www.ncbi.nlm.nih.gov/pubmed/32404906 http://dx.doi.org/10.1038/s41467-020-16169-w |
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author | Lindner, Florian Milne-Davies, Bailey Langenfeld, Katja Stiewe, Thorsten Diepold, Andreas |
author_facet | Lindner, Florian Milne-Davies, Bailey Langenfeld, Katja Stiewe, Thorsten Diepold, Andreas |
author_sort | Lindner, Florian |
collection | PubMed |
description | Many bacteria employ a type III secretion system (T3SS) injectisome to translocate proteins into eukaryotic host cells. Although the T3SS can efficiently export heterologous cargo proteins, a lack of target cell specificity currently limits its application in biotechnology and healthcare. In this study, we exploit the dynamic nature of the T3SS to govern its activity. Using optogenetic interaction switches to control the availability of the dynamic cytosolic T3SS component SctQ, T3SS-dependent effector secretion can be regulated by light. The resulting system, LITESEC-T3SS (Light-induced translocation of effectors through sequestration of endogenous components of the T3SS), allows rapid, specific, and reversible activation or deactivation of the T3SS upon illumination. We demonstrate the light-regulated translocation of heterologous reporter proteins, and induction of apoptosis in cultured eukaryotic cells. LITESEC-T3SS constitutes a new method to control protein secretion and translocation into eukaryotic host cells with unparalleled spatial and temporal resolution. |
format | Online Article Text |
id | pubmed-7221075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72210752020-05-15 LITESEC-T3SS - Light-controlled protein delivery into eukaryotic cells with high spatial and temporal resolution Lindner, Florian Milne-Davies, Bailey Langenfeld, Katja Stiewe, Thorsten Diepold, Andreas Nat Commun Article Many bacteria employ a type III secretion system (T3SS) injectisome to translocate proteins into eukaryotic host cells. Although the T3SS can efficiently export heterologous cargo proteins, a lack of target cell specificity currently limits its application in biotechnology and healthcare. In this study, we exploit the dynamic nature of the T3SS to govern its activity. Using optogenetic interaction switches to control the availability of the dynamic cytosolic T3SS component SctQ, T3SS-dependent effector secretion can be regulated by light. The resulting system, LITESEC-T3SS (Light-induced translocation of effectors through sequestration of endogenous components of the T3SS), allows rapid, specific, and reversible activation or deactivation of the T3SS upon illumination. We demonstrate the light-regulated translocation of heterologous reporter proteins, and induction of apoptosis in cultured eukaryotic cells. LITESEC-T3SS constitutes a new method to control protein secretion and translocation into eukaryotic host cells with unparalleled spatial and temporal resolution. Nature Publishing Group UK 2020-05-13 /pmc/articles/PMC7221075/ /pubmed/32404906 http://dx.doi.org/10.1038/s41467-020-16169-w Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lindner, Florian Milne-Davies, Bailey Langenfeld, Katja Stiewe, Thorsten Diepold, Andreas LITESEC-T3SS - Light-controlled protein delivery into eukaryotic cells with high spatial and temporal resolution |
title | LITESEC-T3SS - Light-controlled protein delivery into eukaryotic cells with high spatial and temporal resolution |
title_full | LITESEC-T3SS - Light-controlled protein delivery into eukaryotic cells with high spatial and temporal resolution |
title_fullStr | LITESEC-T3SS - Light-controlled protein delivery into eukaryotic cells with high spatial and temporal resolution |
title_full_unstemmed | LITESEC-T3SS - Light-controlled protein delivery into eukaryotic cells with high spatial and temporal resolution |
title_short | LITESEC-T3SS - Light-controlled protein delivery into eukaryotic cells with high spatial and temporal resolution |
title_sort | litesec-t3ss - light-controlled protein delivery into eukaryotic cells with high spatial and temporal resolution |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7221075/ https://www.ncbi.nlm.nih.gov/pubmed/32404906 http://dx.doi.org/10.1038/s41467-020-16169-w |
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