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Crosslinked duplex DNA nanogels that target specified proteins
Specific detection of protein biomarkers plays an important role in diagnostics and therapeutics. We have fabricated polymeric nanogels, which can specifically interact with the cancer biomarker thrombin to serve as a model. Two types of 2-methacryloyloxyethyl phosphorylcholine (MPC) copolymers bear...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5101909/ https://www.ncbi.nlm.nih.gov/pubmed/27877881 http://dx.doi.org/10.1080/14686996.2016.1189798 |
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author | Iwasaki, Yasuhiko Kondo, Jun-ichi Kuzuya, Akinori Moriyama, Rui |
author_facet | Iwasaki, Yasuhiko Kondo, Jun-ichi Kuzuya, Akinori Moriyama, Rui |
author_sort | Iwasaki, Yasuhiko |
collection | PubMed |
description | Specific detection of protein biomarkers plays an important role in diagnostics and therapeutics. We have fabricated polymeric nanogels, which can specifically interact with the cancer biomarker thrombin to serve as a model. Two types of 2-methacryloyloxyethyl phosphorylcholine (MPC) copolymers bearing a thrombin-binding oligonucleotide aptamer and its complementary chain were independently synthesized by redox-initiated radical polymerization. These MPC polymers associate in a complimentary fashion due to double strand formation of the oligonucleotides in aqueous media, leading to the spontaneous formation of spherical nanogels. Nanogel formation was confirmed by dynamic light scattering (DLS) and transmittance microscopy. The average size of nanogel particles was 124 ± 2 nm and the nanogels were mono-dispersed (polydispersity index 0.21). Functional intercalators could be stably incorporated into nanogels through the physical interaction between the intercalators and the oligonucleotides. The ethidium bromide (EtBr)-incorporating nanogels were used as detectors for thrombin. The fluorescence intensity of solutions containing the EtBr-incorporating nanogels was decreased with an increase in the concentration of thrombin. The transformation of quadruplex–thrombin structure from complementary double-stranded structures resulted in the decrease in fluorescence intensity. In contrast, the intensity did not change when the nanogels were incubated with albumin. Thrombin is only one such model used to demonstrate this technique; oligonucleotide aptamers can be freely designed to interact with versatile bio-substances. Therefore, aptamer-crosslinked nanogels can be appropriate nanomaterials for disease diagnosis and therapy. |
format | Online Article Text |
id | pubmed-5101909 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-51019092016-11-22 Crosslinked duplex DNA nanogels that target specified proteins Iwasaki, Yasuhiko Kondo, Jun-ichi Kuzuya, Akinori Moriyama, Rui Sci Technol Adv Mater Focus on Nanomedicine molecular science Specific detection of protein biomarkers plays an important role in diagnostics and therapeutics. We have fabricated polymeric nanogels, which can specifically interact with the cancer biomarker thrombin to serve as a model. Two types of 2-methacryloyloxyethyl phosphorylcholine (MPC) copolymers bearing a thrombin-binding oligonucleotide aptamer and its complementary chain were independently synthesized by redox-initiated radical polymerization. These MPC polymers associate in a complimentary fashion due to double strand formation of the oligonucleotides in aqueous media, leading to the spontaneous formation of spherical nanogels. Nanogel formation was confirmed by dynamic light scattering (DLS) and transmittance microscopy. The average size of nanogel particles was 124 ± 2 nm and the nanogels were mono-dispersed (polydispersity index 0.21). Functional intercalators could be stably incorporated into nanogels through the physical interaction between the intercalators and the oligonucleotides. The ethidium bromide (EtBr)-incorporating nanogels were used as detectors for thrombin. The fluorescence intensity of solutions containing the EtBr-incorporating nanogels was decreased with an increase in the concentration of thrombin. The transformation of quadruplex–thrombin structure from complementary double-stranded structures resulted in the decrease in fluorescence intensity. In contrast, the intensity did not change when the nanogels were incubated with albumin. Thrombin is only one such model used to demonstrate this technique; oligonucleotide aptamers can be freely designed to interact with versatile bio-substances. Therefore, aptamer-crosslinked nanogels can be appropriate nanomaterials for disease diagnosis and therapy. Taylor & Francis 2016-07-18 /pmc/articles/PMC5101909/ /pubmed/27877881 http://dx.doi.org/10.1080/14686996.2016.1189798 Text en © 2016 The Author(s). Published by National Institute for Materials Science in partnership with Taylor & Francis http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License(http://creativecommons.org/licenses/by/4.0/),which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Focus on Nanomedicine molecular science Iwasaki, Yasuhiko Kondo, Jun-ichi Kuzuya, Akinori Moriyama, Rui Crosslinked duplex DNA nanogels that target specified proteins |
title | Crosslinked duplex DNA nanogels that target specified proteins |
title_full | Crosslinked duplex DNA nanogels that target specified proteins |
title_fullStr | Crosslinked duplex DNA nanogels that target specified proteins |
title_full_unstemmed | Crosslinked duplex DNA nanogels that target specified proteins |
title_short | Crosslinked duplex DNA nanogels that target specified proteins |
title_sort | crosslinked duplex dna nanogels that target specified proteins |
topic | Focus on Nanomedicine molecular science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5101909/ https://www.ncbi.nlm.nih.gov/pubmed/27877881 http://dx.doi.org/10.1080/14686996.2016.1189798 |
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