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Intracellular chromobody delivery by mesoporous silica nanoparticles for antigen targeting and visualization in real time
Chromobodies have recently drawn great attention as bioimaging nanotools. They offer high antigen binding specificity and affinity comparable to conventional antibodies, but much smaller size and higher stability. Chromobodies can be used in live cell imaging for specific spatio-temporal visualizati...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4865863/ https://www.ncbi.nlm.nih.gov/pubmed/27173765 http://dx.doi.org/10.1038/srep25019 |
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author | Chiu, Hsin-Yi Deng, Wen Engelke, Hanna Helma, Jonas Leonhardt, Heinrich Bein, Thomas |
author_facet | Chiu, Hsin-Yi Deng, Wen Engelke, Hanna Helma, Jonas Leonhardt, Heinrich Bein, Thomas |
author_sort | Chiu, Hsin-Yi |
collection | PubMed |
description | Chromobodies have recently drawn great attention as bioimaging nanotools. They offer high antigen binding specificity and affinity comparable to conventional antibodies, but much smaller size and higher stability. Chromobodies can be used in live cell imaging for specific spatio-temporal visualization of cellular processes. To date, functional application of chromobodies requires lengthy genetic manipulation of the target cell. Here, we develop multifunctional large-pore mesoporous silica nanoparticles (MSNs) as nanocarriers to directly transport chromobodies into living cells for antigen-visualization in real time. The multifunctional large-pore MSNs feature high loading capacity for chromobodies, and are efficiently taken up by cells. By functionalizing the internal MSN surface with nitrilotriacetic acid-metal ion complexes, we can control the release of His(6)-tagged chromobodies from MSNs in acidified endosomes and observe successful chromobody-antigen binding in the cytosol. Hence, by combining the two nanotools, chromobodies and MSNs, we establish a new powerful approach for chromobody applications in living cells. |
format | Online Article Text |
id | pubmed-4865863 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48658632016-05-23 Intracellular chromobody delivery by mesoporous silica nanoparticles for antigen targeting and visualization in real time Chiu, Hsin-Yi Deng, Wen Engelke, Hanna Helma, Jonas Leonhardt, Heinrich Bein, Thomas Sci Rep Article Chromobodies have recently drawn great attention as bioimaging nanotools. They offer high antigen binding specificity and affinity comparable to conventional antibodies, but much smaller size and higher stability. Chromobodies can be used in live cell imaging for specific spatio-temporal visualization of cellular processes. To date, functional application of chromobodies requires lengthy genetic manipulation of the target cell. Here, we develop multifunctional large-pore mesoporous silica nanoparticles (MSNs) as nanocarriers to directly transport chromobodies into living cells for antigen-visualization in real time. The multifunctional large-pore MSNs feature high loading capacity for chromobodies, and are efficiently taken up by cells. By functionalizing the internal MSN surface with nitrilotriacetic acid-metal ion complexes, we can control the release of His(6)-tagged chromobodies from MSNs in acidified endosomes and observe successful chromobody-antigen binding in the cytosol. Hence, by combining the two nanotools, chromobodies and MSNs, we establish a new powerful approach for chromobody applications in living cells. Nature Publishing Group 2016-05-13 /pmc/articles/PMC4865863/ /pubmed/27173765 http://dx.doi.org/10.1038/srep25019 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Chiu, Hsin-Yi Deng, Wen Engelke, Hanna Helma, Jonas Leonhardt, Heinrich Bein, Thomas Intracellular chromobody delivery by mesoporous silica nanoparticles for antigen targeting and visualization in real time |
title | Intracellular chromobody delivery by mesoporous silica nanoparticles for antigen targeting and visualization in real time |
title_full | Intracellular chromobody delivery by mesoporous silica nanoparticles for antigen targeting and visualization in real time |
title_fullStr | Intracellular chromobody delivery by mesoporous silica nanoparticles for antigen targeting and visualization in real time |
title_full_unstemmed | Intracellular chromobody delivery by mesoporous silica nanoparticles for antigen targeting and visualization in real time |
title_short | Intracellular chromobody delivery by mesoporous silica nanoparticles for antigen targeting and visualization in real time |
title_sort | intracellular chromobody delivery by mesoporous silica nanoparticles for antigen targeting and visualization in real time |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4865863/ https://www.ncbi.nlm.nih.gov/pubmed/27173765 http://dx.doi.org/10.1038/srep25019 |
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