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Sequentially Programmable and Cellularly Selective Assembly of Fluorescent Polymerized Vesicles for Monitoring Cell Apoptosis
The introduction of controlled self‐assembly into living organisms opens up desired biomedical applications in wide areas including bioimaging/assays, drug delivery, and tissue engineering. Besides the enzyme‐activated examples reported before, controlled self‐assembly under integrated stimuli, espe...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700639/ https://www.ncbi.nlm.nih.gov/pubmed/29201625 http://dx.doi.org/10.1002/advs.201700310 |
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author | Peng, Shu Pan, Yu‐Chen Wang, Yaling Xu, Zhe Chen, Chao Ding, Dan Wang, Yongjian Guo, Dong‐Sheng |
author_facet | Peng, Shu Pan, Yu‐Chen Wang, Yaling Xu, Zhe Chen, Chao Ding, Dan Wang, Yongjian Guo, Dong‐Sheng |
author_sort | Peng, Shu |
collection | PubMed |
description | The introduction of controlled self‐assembly into living organisms opens up desired biomedical applications in wide areas including bioimaging/assays, drug delivery, and tissue engineering. Besides the enzyme‐activated examples reported before, controlled self‐assembly under integrated stimuli, especially in the form of sequential input, is unprecedented and ultimately challenging. This study reports a programmable self‐assembling strategy in living cells under sequentially integrated control of both endogenous and exogenous stimuli. Fluorescent polymerized vesicles are constructed by using cholinesterase conversion followed by photopolymerization and thermochromism. Furthermore, as a proof‐of‐principle application, the cell apoptosis involved in the overexpression of cholinesterase in virtue of the generated fluorescence is monitored, showing potential in screening apoptosis‐inducing drugs. The approach exhibits multiple advantages for bioimaging in living cells, including specificity to cholinesterase, red emission, wash free, high signal‐to‐noise ratio. |
format | Online Article Text |
id | pubmed-5700639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57006392017-11-30 Sequentially Programmable and Cellularly Selective Assembly of Fluorescent Polymerized Vesicles for Monitoring Cell Apoptosis Peng, Shu Pan, Yu‐Chen Wang, Yaling Xu, Zhe Chen, Chao Ding, Dan Wang, Yongjian Guo, Dong‐Sheng Adv Sci (Weinh) Full Papers The introduction of controlled self‐assembly into living organisms opens up desired biomedical applications in wide areas including bioimaging/assays, drug delivery, and tissue engineering. Besides the enzyme‐activated examples reported before, controlled self‐assembly under integrated stimuli, especially in the form of sequential input, is unprecedented and ultimately challenging. This study reports a programmable self‐assembling strategy in living cells under sequentially integrated control of both endogenous and exogenous stimuli. Fluorescent polymerized vesicles are constructed by using cholinesterase conversion followed by photopolymerization and thermochromism. Furthermore, as a proof‐of‐principle application, the cell apoptosis involved in the overexpression of cholinesterase in virtue of the generated fluorescence is monitored, showing potential in screening apoptosis‐inducing drugs. The approach exhibits multiple advantages for bioimaging in living cells, including specificity to cholinesterase, red emission, wash free, high signal‐to‐noise ratio. John Wiley and Sons Inc. 2017-08-10 /pmc/articles/PMC5700639/ /pubmed/29201625 http://dx.doi.org/10.1002/advs.201700310 Text en © 2017 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Peng, Shu Pan, Yu‐Chen Wang, Yaling Xu, Zhe Chen, Chao Ding, Dan Wang, Yongjian Guo, Dong‐Sheng Sequentially Programmable and Cellularly Selective Assembly of Fluorescent Polymerized Vesicles for Monitoring Cell Apoptosis |
title | Sequentially Programmable and Cellularly Selective Assembly of Fluorescent Polymerized Vesicles for Monitoring Cell Apoptosis |
title_full | Sequentially Programmable and Cellularly Selective Assembly of Fluorescent Polymerized Vesicles for Monitoring Cell Apoptosis |
title_fullStr | Sequentially Programmable and Cellularly Selective Assembly of Fluorescent Polymerized Vesicles for Monitoring Cell Apoptosis |
title_full_unstemmed | Sequentially Programmable and Cellularly Selective Assembly of Fluorescent Polymerized Vesicles for Monitoring Cell Apoptosis |
title_short | Sequentially Programmable and Cellularly Selective Assembly of Fluorescent Polymerized Vesicles for Monitoring Cell Apoptosis |
title_sort | sequentially programmable and cellularly selective assembly of fluorescent polymerized vesicles for monitoring cell apoptosis |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700639/ https://www.ncbi.nlm.nih.gov/pubmed/29201625 http://dx.doi.org/10.1002/advs.201700310 |
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