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A bacterial type III secretion-based protein delivery tool for broad applications in cell biology
Methods enabling the delivery of proteins into eukaryotic cells are essential to address protein functions. Here we propose broad applications to cell biology for a protein delivery tool based on bacterial type III secretion (T3S). We show that bacterial, viral, and human proteins, fused to the N-te...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4657163/ https://www.ncbi.nlm.nih.gov/pubmed/26598622 http://dx.doi.org/10.1083/jcb.201502074 |
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author | Ittig, Simon J. Schmutz, Christoph Kasper, Christoph A. Amstutz, Marlise Schmidt, Alexander Sauteur, Loïc Vigano, M. Alessandra Low, Shyan Huey Affolter, Markus Cornelis, Guy R. Nigg, Erich A. Arrieumerlou, Cécile |
author_facet | Ittig, Simon J. Schmutz, Christoph Kasper, Christoph A. Amstutz, Marlise Schmidt, Alexander Sauteur, Loïc Vigano, M. Alessandra Low, Shyan Huey Affolter, Markus Cornelis, Guy R. Nigg, Erich A. Arrieumerlou, Cécile |
author_sort | Ittig, Simon J. |
collection | PubMed |
description | Methods enabling the delivery of proteins into eukaryotic cells are essential to address protein functions. Here we propose broad applications to cell biology for a protein delivery tool based on bacterial type III secretion (T3S). We show that bacterial, viral, and human proteins, fused to the N-terminal fragment of the Yersinia enterocolitica T3S substrate YopE, are effectively delivered into target cells in a fast and controllable manner via the injectisome of extracellular bacteria. This method enables functional interaction studies by the simultaneous injection of multiple proteins and allows the targeting of proteins to different subcellular locations by use of nanobody-fusion proteins. After delivery, proteins can be freed from the YopE fragment by a T3S-translocated viral protease or fusion to ubiquitin and cleavage by endogenous ubiquitin proteases. Finally, we show that this delivery tool is suitable to inject proteins in living animals and combine it with phosphoproteomics to characterize the systems-level impact of proapoptotic human truncated BID on the cellular network. |
format | Online Article Text |
id | pubmed-4657163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-46571632016-05-23 A bacterial type III secretion-based protein delivery tool for broad applications in cell biology Ittig, Simon J. Schmutz, Christoph Kasper, Christoph A. Amstutz, Marlise Schmidt, Alexander Sauteur, Loïc Vigano, M. Alessandra Low, Shyan Huey Affolter, Markus Cornelis, Guy R. Nigg, Erich A. Arrieumerlou, Cécile J Cell Biol Research Articles Methods enabling the delivery of proteins into eukaryotic cells are essential to address protein functions. Here we propose broad applications to cell biology for a protein delivery tool based on bacterial type III secretion (T3S). We show that bacterial, viral, and human proteins, fused to the N-terminal fragment of the Yersinia enterocolitica T3S substrate YopE, are effectively delivered into target cells in a fast and controllable manner via the injectisome of extracellular bacteria. This method enables functional interaction studies by the simultaneous injection of multiple proteins and allows the targeting of proteins to different subcellular locations by use of nanobody-fusion proteins. After delivery, proteins can be freed from the YopE fragment by a T3S-translocated viral protease or fusion to ubiquitin and cleavage by endogenous ubiquitin proteases. Finally, we show that this delivery tool is suitable to inject proteins in living animals and combine it with phosphoproteomics to characterize the systems-level impact of proapoptotic human truncated BID on the cellular network. The Rockefeller University Press 2015-11-23 /pmc/articles/PMC4657163/ /pubmed/26598622 http://dx.doi.org/10.1083/jcb.201502074 Text en © 2015 Ittig et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Ittig, Simon J. Schmutz, Christoph Kasper, Christoph A. Amstutz, Marlise Schmidt, Alexander Sauteur, Loïc Vigano, M. Alessandra Low, Shyan Huey Affolter, Markus Cornelis, Guy R. Nigg, Erich A. Arrieumerlou, Cécile A bacterial type III secretion-based protein delivery tool for broad applications in cell biology |
title | A bacterial type III secretion-based protein delivery tool for broad applications in cell biology |
title_full | A bacterial type III secretion-based protein delivery tool for broad applications in cell biology |
title_fullStr | A bacterial type III secretion-based protein delivery tool for broad applications in cell biology |
title_full_unstemmed | A bacterial type III secretion-based protein delivery tool for broad applications in cell biology |
title_short | A bacterial type III secretion-based protein delivery tool for broad applications in cell biology |
title_sort | bacterial type iii secretion-based protein delivery tool for broad applications in cell biology |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4657163/ https://www.ncbi.nlm.nih.gov/pubmed/26598622 http://dx.doi.org/10.1083/jcb.201502074 |
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