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“Turn-on” fluorescence probe integrated polymer nanoparticles for sensing biological thiol molecules

A “turn-on” thiol-responsive fluorescence probe was synthesized and integrated into polymeric nanoparticles for sensing intracellular thiols. There is a photo-induced electron transfer process in the off state of the probe, and this process is terminated upon the reaction with thiol compounds. Confi...

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Autores principales: Ang, Chung Yen, Tan, Si Yu, Lu, Yunpeng, Bai, Linyi, Li, Menghuan, Li, Peizhou, Zhang, Quan, Selvan, Subramanian Tamil, Zhao, Yanli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231329/
https://www.ncbi.nlm.nih.gov/pubmed/25394758
http://dx.doi.org/10.1038/srep07057
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author Ang, Chung Yen
Tan, Si Yu
Lu, Yunpeng
Bai, Linyi
Li, Menghuan
Li, Peizhou
Zhang, Quan
Selvan, Subramanian Tamil
Zhao, Yanli
author_facet Ang, Chung Yen
Tan, Si Yu
Lu, Yunpeng
Bai, Linyi
Li, Menghuan
Li, Peizhou
Zhang, Quan
Selvan, Subramanian Tamil
Zhao, Yanli
author_sort Ang, Chung Yen
collection PubMed
description A “turn-on” thiol-responsive fluorescence probe was synthesized and integrated into polymeric nanoparticles for sensing intracellular thiols. There is a photo-induced electron transfer process in the off state of the probe, and this process is terminated upon the reaction with thiol compounds. Configuration interaction singles (CIS) calculation was performed to confirm the mechanism of this process. A series of sensing studies were carried out, showing that the probe-integrated nanoparticles were highly selective towards biological thiol compounds over non-thiolated amino acids. Kinetic studies were also performed to investigate the relative reaction rate between the probe and the thiolated amino acids. Subsequently, the Gibbs free energy of the reactions was explored by means of the electrochemical method. Finally, the detection system was employed for sensing intracellular thiols in cancer cells, and the sensing selectivity could be further enhanced with the use of a cancer cell-targeting ligand in the nanoparticles. This development paves a path for the sensing and detection of biological thiols, serving as a potential diagnostic tool in the future.
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spelling pubmed-42313292014-11-17 “Turn-on” fluorescence probe integrated polymer nanoparticles for sensing biological thiol molecules Ang, Chung Yen Tan, Si Yu Lu, Yunpeng Bai, Linyi Li, Menghuan Li, Peizhou Zhang, Quan Selvan, Subramanian Tamil Zhao, Yanli Sci Rep Article A “turn-on” thiol-responsive fluorescence probe was synthesized and integrated into polymeric nanoparticles for sensing intracellular thiols. There is a photo-induced electron transfer process in the off state of the probe, and this process is terminated upon the reaction with thiol compounds. Configuration interaction singles (CIS) calculation was performed to confirm the mechanism of this process. A series of sensing studies were carried out, showing that the probe-integrated nanoparticles were highly selective towards biological thiol compounds over non-thiolated amino acids. Kinetic studies were also performed to investigate the relative reaction rate between the probe and the thiolated amino acids. Subsequently, the Gibbs free energy of the reactions was explored by means of the electrochemical method. Finally, the detection system was employed for sensing intracellular thiols in cancer cells, and the sensing selectivity could be further enhanced with the use of a cancer cell-targeting ligand in the nanoparticles. This development paves a path for the sensing and detection of biological thiols, serving as a potential diagnostic tool in the future. Nature Publishing Group 2014-11-14 /pmc/articles/PMC4231329/ /pubmed/25394758 http://dx.doi.org/10.1038/srep07057 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 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 in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Article
Ang, Chung Yen
Tan, Si Yu
Lu, Yunpeng
Bai, Linyi
Li, Menghuan
Li, Peizhou
Zhang, Quan
Selvan, Subramanian Tamil
Zhao, Yanli
“Turn-on” fluorescence probe integrated polymer nanoparticles for sensing biological thiol molecules
title “Turn-on” fluorescence probe integrated polymer nanoparticles for sensing biological thiol molecules
title_full “Turn-on” fluorescence probe integrated polymer nanoparticles for sensing biological thiol molecules
title_fullStr “Turn-on” fluorescence probe integrated polymer nanoparticles for sensing biological thiol molecules
title_full_unstemmed “Turn-on” fluorescence probe integrated polymer nanoparticles for sensing biological thiol molecules
title_short “Turn-on” fluorescence probe integrated polymer nanoparticles for sensing biological thiol molecules
title_sort “turn-on” fluorescence probe integrated polymer nanoparticles for sensing biological thiol molecules
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231329/
https://www.ncbi.nlm.nih.gov/pubmed/25394758
http://dx.doi.org/10.1038/srep07057
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