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Stimuli-responsive nucleic acid-functionalized metal–organic framework nanoparticles using pH- and metal-ion-dependent DNAzymes as locks

A versatile approach to modify metal–organic framework nanoparticles (NMOFs) with nucleic acid tethers, using the “click chemistry” method is introduced. The nucleic acid-functionalized NMOFs are used to prepare stimuli-responsive carriers of loads (fluorescence probes or anti-cancer drugs). Two dif...

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Autores principales: Chen, Wei-Hai, Yu, Xu, Cecconello, Alessandro, Sohn, Yang Sung, Nechushtai, Rachel, Willner, Itamar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5621505/
https://www.ncbi.nlm.nih.gov/pubmed/28989617
http://dx.doi.org/10.1039/c7sc01765k
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author Chen, Wei-Hai
Yu, Xu
Cecconello, Alessandro
Sohn, Yang Sung
Nechushtai, Rachel
Willner, Itamar
author_facet Chen, Wei-Hai
Yu, Xu
Cecconello, Alessandro
Sohn, Yang Sung
Nechushtai, Rachel
Willner, Itamar
author_sort Chen, Wei-Hai
collection PubMed
description A versatile approach to modify metal–organic framework nanoparticles (NMOFs) with nucleic acid tethers, using the “click chemistry” method is introduced. The nucleic acid-functionalized NMOFs are used to prepare stimuli-responsive carriers of loads (fluorescence probes or anti-cancer drugs). Two different stimuli-responsive nucleic acid-based NMOFs are presented. One system involves the preparation of pH-responsive NMOFs. The NMOFs are loaded with fluorophores or doxorubicin anti-cancer drug and locked in the NMOFs by pH-responsive DNA duplex capping units. At pH = 5.0 the capping units are unlocked, leading to the release of the loads. The AS1411 aptamer is conjugated to the locking units as the targeting unit for the nucleolin biomarker present in cancer cells. The pH-responsive doxorubicin-loaded NMOFs and, in particular, the AS1411 aptamer-modified pH-responsive NMOFs reveal selective, targeted, cytotoxicity toward MDA-MB-231 breast cancer cells. A second system involves the synthesis of NMOFs that are loaded with fluorophores or doxorubicin and capped with metal-ion-dependent DNAzyme/substrate complexes as locking units (metal ion = Mg(2+) or Pb(2+) ions). In the presence of the respective metal ions, the nucleic acid locking units are cleaved off, resulting in the release of the loads. Also, “smart” Mg(2+)-ion-dependent DNAzyme capped doxorubicin-loaded NMOFs are synthesized via the integration of the ATP aptamer sequence in the loop domain of the Mg(2+)-dependent DNAzyme. The unlocking of these NMOFs proceeds effectively only in the presence of ATP and Mg(2+) ions, acting as cooperative triggers. As ATP is over-expressed in cancer cells, the “smart” carrier provides sense-and-treat functions. The “smart” ATP/Mg(2+)-triggered doxorubicin-loaded NMOFs reveal selective cytotoxicity toward MDA-MB-231 cancer cells. Beyond the use of the metal-ion-dependent DNAzymes as ion-responsive locks of drug-loaded NMOF carriers, the DNAzyme-capped fluorophore-loaded NMOFs are successfully applied as functional units for multiplexed ion-sensing and for the design of logic-gate systems.
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spelling pubmed-56215052017-10-06 Stimuli-responsive nucleic acid-functionalized metal–organic framework nanoparticles using pH- and metal-ion-dependent DNAzymes as locks Chen, Wei-Hai Yu, Xu Cecconello, Alessandro Sohn, Yang Sung Nechushtai, Rachel Willner, Itamar Chem Sci Chemistry A versatile approach to modify metal–organic framework nanoparticles (NMOFs) with nucleic acid tethers, using the “click chemistry” method is introduced. The nucleic acid-functionalized NMOFs are used to prepare stimuli-responsive carriers of loads (fluorescence probes or anti-cancer drugs). Two different stimuli-responsive nucleic acid-based NMOFs are presented. One system involves the preparation of pH-responsive NMOFs. The NMOFs are loaded with fluorophores or doxorubicin anti-cancer drug and locked in the NMOFs by pH-responsive DNA duplex capping units. At pH = 5.0 the capping units are unlocked, leading to the release of the loads. The AS1411 aptamer is conjugated to the locking units as the targeting unit for the nucleolin biomarker present in cancer cells. The pH-responsive doxorubicin-loaded NMOFs and, in particular, the AS1411 aptamer-modified pH-responsive NMOFs reveal selective, targeted, cytotoxicity toward MDA-MB-231 breast cancer cells. A second system involves the synthesis of NMOFs that are loaded with fluorophores or doxorubicin and capped with metal-ion-dependent DNAzyme/substrate complexes as locking units (metal ion = Mg(2+) or Pb(2+) ions). In the presence of the respective metal ions, the nucleic acid locking units are cleaved off, resulting in the release of the loads. Also, “smart” Mg(2+)-ion-dependent DNAzyme capped doxorubicin-loaded NMOFs are synthesized via the integration of the ATP aptamer sequence in the loop domain of the Mg(2+)-dependent DNAzyme. The unlocking of these NMOFs proceeds effectively only in the presence of ATP and Mg(2+) ions, acting as cooperative triggers. As ATP is over-expressed in cancer cells, the “smart” carrier provides sense-and-treat functions. The “smart” ATP/Mg(2+)-triggered doxorubicin-loaded NMOFs reveal selective cytotoxicity toward MDA-MB-231 cancer cells. Beyond the use of the metal-ion-dependent DNAzymes as ion-responsive locks of drug-loaded NMOF carriers, the DNAzyme-capped fluorophore-loaded NMOFs are successfully applied as functional units for multiplexed ion-sensing and for the design of logic-gate systems. Royal Society of Chemistry 2017-08-01 2017-06-06 /pmc/articles/PMC5621505/ /pubmed/28989617 http://dx.doi.org/10.1039/c7sc01765k Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Chen, Wei-Hai
Yu, Xu
Cecconello, Alessandro
Sohn, Yang Sung
Nechushtai, Rachel
Willner, Itamar
Stimuli-responsive nucleic acid-functionalized metal–organic framework nanoparticles using pH- and metal-ion-dependent DNAzymes as locks
title Stimuli-responsive nucleic acid-functionalized metal–organic framework nanoparticles using pH- and metal-ion-dependent DNAzymes as locks
title_full Stimuli-responsive nucleic acid-functionalized metal–organic framework nanoparticles using pH- and metal-ion-dependent DNAzymes as locks
title_fullStr Stimuli-responsive nucleic acid-functionalized metal–organic framework nanoparticles using pH- and metal-ion-dependent DNAzymes as locks
title_full_unstemmed Stimuli-responsive nucleic acid-functionalized metal–organic framework nanoparticles using pH- and metal-ion-dependent DNAzymes as locks
title_short Stimuli-responsive nucleic acid-functionalized metal–organic framework nanoparticles using pH- and metal-ion-dependent DNAzymes as locks
title_sort stimuli-responsive nucleic acid-functionalized metal–organic framework nanoparticles using ph- and metal-ion-dependent dnazymes as locks
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5621505/
https://www.ncbi.nlm.nih.gov/pubmed/28989617
http://dx.doi.org/10.1039/c7sc01765k
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