Molecular imaging of telomerase and the enzyme activity-triggered drug release by using a conformation-switchable nanoprobe in cancerous cells

Abstract So far, the development of a unique strategy for specific biomolecules activity monitoring and precise drugs release in cancerous cells is still challenging. Here, we designed a conformation-switchable smart nanoprobe to monitor telomerase activity and to enable activity-triggered drug rele...

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Autores principales: Hai Shi, Tao Gao, Liu Shi, Tianshu Chen, Yang Xiang, Yuanyang Li, Genxi Li
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2018
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Acceso en línea:https://doaj.org/article/6fb2933b73d94e3da40323bd09cfe140
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spelling oai:doaj.org-article:6fb2933b73d94e3da40323bd09cfe1402021-12-02T15:08:41ZMolecular imaging of telomerase and the enzyme activity-triggered drug release by using a conformation-switchable nanoprobe in cancerous cells10.1038/s41598-018-34670-72045-2322https://doaj.org/article/6fb2933b73d94e3da40323bd09cfe1402018-11-01T00:00:00Zhttps://doi.org/10.1038/s41598-018-34670-7https://doaj.org/toc/2045-2322Abstract So far, the development of a unique strategy for specific biomolecules activity monitoring and precise drugs release in cancerous cells is still challenging. Here, we designed a conformation-switchable smart nanoprobe to monitor telomerase activity and to enable activity-triggered drug release in cancerous cells. The straightforward nanoprobe contained a gold nanoparticle (AuNP) core and a dense layer of 5-carboxyfluorescein (FAM)-labeled hairpin DNA shell. The 3′ region of hairpin DNA sequence could function as the telomerase primer to be elongated in the presence of telomerase, resulting in the conformational switch of hairpin DNA. As a result, the FAM fluorescence was activated and the anticancer drug doxorubicin (Dox) molecules which intercalated into the stem region of the hairpin DNA sequence were released into cancerous cells simultaneously. The smart method could specifically distinguish cancerous cells from normal cells based on telomerase activity. It also showed a good performance for monitoring telomerase activity in the cytoplasm by molecular imaging and precise release of Dox triggered by telomerase activity in cancerous cells. These advantages may offer a great potential of this method for monitoring telomerase activity in cancer progression and estimating therapeutic effect.Hai ShiTao GaoLiu ShiTianshu ChenYang XiangYuanyang LiGenxi LiNature PortfolioarticleNanoprobesTelomerase ActivityTRAP Reaction BufferTelomerase ExtractTelomeric Repeat Amplification Protocol (TRAP)MedicineRScienceQENScientific Reports, Vol 8, Iss 1, Pp 1-11 (2018)
institution DOAJ
collection DOAJ
language EN
topic Nanoprobes
Telomerase Activity
TRAP Reaction Buffer
Telomerase Extract
Telomeric Repeat Amplification Protocol (TRAP)
Medicine
R
Science
Q
spellingShingle Nanoprobes
Telomerase Activity
TRAP Reaction Buffer
Telomerase Extract
Telomeric Repeat Amplification Protocol (TRAP)
Medicine
R
Science
Q
Hai Shi
Tao Gao
Liu Shi
Tianshu Chen
Yang Xiang
Yuanyang Li
Genxi Li
Molecular imaging of telomerase and the enzyme activity-triggered drug release by using a conformation-switchable nanoprobe in cancerous cells
description Abstract So far, the development of a unique strategy for specific biomolecules activity monitoring and precise drugs release in cancerous cells is still challenging. Here, we designed a conformation-switchable smart nanoprobe to monitor telomerase activity and to enable activity-triggered drug release in cancerous cells. The straightforward nanoprobe contained a gold nanoparticle (AuNP) core and a dense layer of 5-carboxyfluorescein (FAM)-labeled hairpin DNA shell. The 3′ region of hairpin DNA sequence could function as the telomerase primer to be elongated in the presence of telomerase, resulting in the conformational switch of hairpin DNA. As a result, the FAM fluorescence was activated and the anticancer drug doxorubicin (Dox) molecules which intercalated into the stem region of the hairpin DNA sequence were released into cancerous cells simultaneously. The smart method could specifically distinguish cancerous cells from normal cells based on telomerase activity. It also showed a good performance for monitoring telomerase activity in the cytoplasm by molecular imaging and precise release of Dox triggered by telomerase activity in cancerous cells. These advantages may offer a great potential of this method for monitoring telomerase activity in cancer progression and estimating therapeutic effect.
format article
author Hai Shi
Tao Gao
Liu Shi
Tianshu Chen
Yang Xiang
Yuanyang Li
Genxi Li
author_facet Hai Shi
Tao Gao
Liu Shi
Tianshu Chen
Yang Xiang
Yuanyang Li
Genxi Li
author_sort Hai Shi
title Molecular imaging of telomerase and the enzyme activity-triggered drug release by using a conformation-switchable nanoprobe in cancerous cells
title_short Molecular imaging of telomerase and the enzyme activity-triggered drug release by using a conformation-switchable nanoprobe in cancerous cells
title_full Molecular imaging of telomerase and the enzyme activity-triggered drug release by using a conformation-switchable nanoprobe in cancerous cells
title_fullStr Molecular imaging of telomerase and the enzyme activity-triggered drug release by using a conformation-switchable nanoprobe in cancerous cells
title_full_unstemmed Molecular imaging of telomerase and the enzyme activity-triggered drug release by using a conformation-switchable nanoprobe in cancerous cells
title_sort molecular imaging of telomerase and the enzyme activity-triggered drug release by using a conformation-switchable nanoprobe in cancerous cells
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/6fb2933b73d94e3da40323bd09cfe140
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AT taogao molecularimagingoftelomeraseandtheenzymeactivitytriggereddrugreleasebyusingaconformationswitchablenanoprobeincancerouscells
AT liushi molecularimagingoftelomeraseandtheenzymeactivitytriggereddrugreleasebyusingaconformationswitchablenanoprobeincancerouscells
AT tianshuchen molecularimagingoftelomeraseandtheenzymeactivitytriggereddrugreleasebyusingaconformationswitchablenanoprobeincancerouscells
AT yangxiang molecularimagingoftelomeraseandtheenzymeactivitytriggereddrugreleasebyusingaconformationswitchablenanoprobeincancerouscells
AT yuanyangli molecularimagingoftelomeraseandtheenzymeactivitytriggereddrugreleasebyusingaconformationswitchablenanoprobeincancerouscells
AT genxili molecularimagingoftelomeraseandtheenzymeactivitytriggereddrugreleasebyusingaconformationswitchablenanoprobeincancerouscells
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