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Bimodal fluorogenic sensing of matrix proteolytic signatures in lung cancer

Optical biosensing based on the activation of fluorescent reporters offers a powerful methodology for the real-time molecular interrogation of pathology. Here we report a first-in-class, bimodal fluorescent reporter strategy for the simultaneous and highly specific detection of two independent prote...

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Detalles Bibliográficos
Autores principales: Megia-Fernandez, Alicia, Mills, Bethany, Michels, Chesney, Chankeshwara, Sunay V., Krstajić, Nikola, Haslett, Chris, Dhaliwal, Kevin, Bradley, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238727/
https://www.ncbi.nlm.nih.gov/pubmed/30175355
http://dx.doi.org/10.1039/c8ob01790e
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author Megia-Fernandez, Alicia
Mills, Bethany
Michels, Chesney
Chankeshwara, Sunay V.
Krstajić, Nikola
Haslett, Chris
Dhaliwal, Kevin
Bradley, Mark
author_facet Megia-Fernandez, Alicia
Mills, Bethany
Michels, Chesney
Chankeshwara, Sunay V.
Krstajić, Nikola
Haslett, Chris
Dhaliwal, Kevin
Bradley, Mark
author_sort Megia-Fernandez, Alicia
collection PubMed
description Optical biosensing based on the activation of fluorescent reporters offers a powerful methodology for the real-time molecular interrogation of pathology. Here we report a first-in-class, bimodal fluorescent reporter strategy for the simultaneous and highly specific detection of two independent proteases (thrombin and matrix metalloproteases (MMPs)) pivotal in the fibroproliferative process surrounding lung cancer, based on a dual, multiplexing, peptide FRET system. This sophisticated synthetic smartprobe, with a molecular weight of 6 kDa, contains two independent fluorophores and quenchers that generate photonic signatures at two specific wavelengths upon activation by target enzymes within human lung cancer tissue.
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spelling pubmed-62387272018-12-12 Bimodal fluorogenic sensing of matrix proteolytic signatures in lung cancer Megia-Fernandez, Alicia Mills, Bethany Michels, Chesney Chankeshwara, Sunay V. Krstajić, Nikola Haslett, Chris Dhaliwal, Kevin Bradley, Mark Org Biomol Chem Chemistry Optical biosensing based on the activation of fluorescent reporters offers a powerful methodology for the real-time molecular interrogation of pathology. Here we report a first-in-class, bimodal fluorescent reporter strategy for the simultaneous and highly specific detection of two independent proteases (thrombin and matrix metalloproteases (MMPs)) pivotal in the fibroproliferative process surrounding lung cancer, based on a dual, multiplexing, peptide FRET system. This sophisticated synthetic smartprobe, with a molecular weight of 6 kDa, contains two independent fluorophores and quenchers that generate photonic signatures at two specific wavelengths upon activation by target enzymes within human lung cancer tissue. Royal Society of Chemistry 2018-11-21 2018-08-23 /pmc/articles/PMC6238727/ /pubmed/30175355 http://dx.doi.org/10.1039/c8ob01790e Text en This journal is © The Royal Society of Chemistry 2018 https://creativecommons.org/licenses/by/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Megia-Fernandez, Alicia
Mills, Bethany
Michels, Chesney
Chankeshwara, Sunay V.
Krstajić, Nikola
Haslett, Chris
Dhaliwal, Kevin
Bradley, Mark
Bimodal fluorogenic sensing of matrix proteolytic signatures in lung cancer
title Bimodal fluorogenic sensing of matrix proteolytic signatures in lung cancer
title_full Bimodal fluorogenic sensing of matrix proteolytic signatures in lung cancer
title_fullStr Bimodal fluorogenic sensing of matrix proteolytic signatures in lung cancer
title_full_unstemmed Bimodal fluorogenic sensing of matrix proteolytic signatures in lung cancer
title_short Bimodal fluorogenic sensing of matrix proteolytic signatures in lung cancer
title_sort bimodal fluorogenic sensing of matrix proteolytic signatures in lung cancer
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238727/
https://www.ncbi.nlm.nih.gov/pubmed/30175355
http://dx.doi.org/10.1039/c8ob01790e
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