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Fabrication of device with poly(N-isopropylacrylamide)-b-ssDNA copolymer brush for resistivity study

In this study, we grafted bromo-terminated poly(N-isopropylacrylamide) (PNIPAAm) brushes onto thin gold films deposited on silicon, and then reacted with NaN(3) to produce azido-terminated PNIPAAm brushes. A probe sequence of single-stranded DNA (ssDNA) with a 4-pentynoic acid succinimidyl ester uni...

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Autores principales: Liu, Yi-Zu, Chen, May-Show, Cheng, Chih-Chia, Chen, Shih-Hsun, Chen, Jem-Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5629771/
https://www.ncbi.nlm.nih.gov/pubmed/28982368
http://dx.doi.org/10.1186/s12951-017-0303-4
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author Liu, Yi-Zu
Chen, May-Show
Cheng, Chih-Chia
Chen, Shih-Hsun
Chen, Jem-Kun
author_facet Liu, Yi-Zu
Chen, May-Show
Cheng, Chih-Chia
Chen, Shih-Hsun
Chen, Jem-Kun
author_sort Liu, Yi-Zu
collection PubMed
description In this study, we grafted bromo-terminated poly(N-isopropylacrylamide) (PNIPAAm) brushes onto thin gold films deposited on silicon, and then reacted with NaN(3) to produce azido-terminated PNIPAAm brushes. A probe sequence of single-stranded DNA (ssDNA) with a 4-pentynoic acid succinimidyl ester unit was grafted onto the azido-terminated PNIPAAm brushes through a click reaction, resulting in the formation of block copolymer brushes. The PNIPAAm-b-ssDNA copolymer brushes formed supramolecular complexes stabilized by bio-multiple hydrogen bonds (BMHBs), which enhanced the proton transfer and thereby decreased the resistivity of the structures. In addition, the optimal operation window for DNA detection ranges from 0 to 0.2 M of NaCl concentration. Therefore, the specimens were prepared in the PBS solution at 150 mM NaCl concentration for target hybridization. The supramolecular complex state of the PNIPAAm-b-ssDNA copolymer brushes transformed into the phase-separated state after the hybridization with 0.5 ng/µL of its target DNA sequence owing to the competition between BMHBs and complementary hydrogen bonds. This phase transformation of the PNIPAAm and probe segments inhibited the proton transfer and significantly increased the resistivity at 25 °C. Moreover, there were no significant changes in the resistivity of the copolymer brushes after hybridization with the target sequence at 45 °C. These results indicated that the phase-separated state of the PNIPAAm-b-ssDNA copolymer brushes, which was generally occurred above the LCST, can be substantially generated after hybridization with its target DNA sequence. By performing the controlled experiments, in the same manner, using another sequence with lengths similar to that of the target sequence without complementarity. In addition, the sequences featuring various degrees of complementarity were exploited to verify the phase separation behavior inside the PNIPAAm-b-ssDNA copolymer thin film. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12951-017-0303-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-56297712017-10-13 Fabrication of device with poly(N-isopropylacrylamide)-b-ssDNA copolymer brush for resistivity study Liu, Yi-Zu Chen, May-Show Cheng, Chih-Chia Chen, Shih-Hsun Chen, Jem-Kun J Nanobiotechnology Research In this study, we grafted bromo-terminated poly(N-isopropylacrylamide) (PNIPAAm) brushes onto thin gold films deposited on silicon, and then reacted with NaN(3) to produce azido-terminated PNIPAAm brushes. A probe sequence of single-stranded DNA (ssDNA) with a 4-pentynoic acid succinimidyl ester unit was grafted onto the azido-terminated PNIPAAm brushes through a click reaction, resulting in the formation of block copolymer brushes. The PNIPAAm-b-ssDNA copolymer brushes formed supramolecular complexes stabilized by bio-multiple hydrogen bonds (BMHBs), which enhanced the proton transfer and thereby decreased the resistivity of the structures. In addition, the optimal operation window for DNA detection ranges from 0 to 0.2 M of NaCl concentration. Therefore, the specimens were prepared in the PBS solution at 150 mM NaCl concentration for target hybridization. The supramolecular complex state of the PNIPAAm-b-ssDNA copolymer brushes transformed into the phase-separated state after the hybridization with 0.5 ng/µL of its target DNA sequence owing to the competition between BMHBs and complementary hydrogen bonds. This phase transformation of the PNIPAAm and probe segments inhibited the proton transfer and significantly increased the resistivity at 25 °C. Moreover, there were no significant changes in the resistivity of the copolymer brushes after hybridization with the target sequence at 45 °C. These results indicated that the phase-separated state of the PNIPAAm-b-ssDNA copolymer brushes, which was generally occurred above the LCST, can be substantially generated after hybridization with its target DNA sequence. By performing the controlled experiments, in the same manner, using another sequence with lengths similar to that of the target sequence without complementarity. In addition, the sequences featuring various degrees of complementarity were exploited to verify the phase separation behavior inside the PNIPAAm-b-ssDNA copolymer thin film. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12951-017-0303-4) contains supplementary material, which is available to authorized users. BioMed Central 2017-10-05 /pmc/articles/PMC5629771/ /pubmed/28982368 http://dx.doi.org/10.1186/s12951-017-0303-4 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Liu, Yi-Zu
Chen, May-Show
Cheng, Chih-Chia
Chen, Shih-Hsun
Chen, Jem-Kun
Fabrication of device with poly(N-isopropylacrylamide)-b-ssDNA copolymer brush for resistivity study
title Fabrication of device with poly(N-isopropylacrylamide)-b-ssDNA copolymer brush for resistivity study
title_full Fabrication of device with poly(N-isopropylacrylamide)-b-ssDNA copolymer brush for resistivity study
title_fullStr Fabrication of device with poly(N-isopropylacrylamide)-b-ssDNA copolymer brush for resistivity study
title_full_unstemmed Fabrication of device with poly(N-isopropylacrylamide)-b-ssDNA copolymer brush for resistivity study
title_short Fabrication of device with poly(N-isopropylacrylamide)-b-ssDNA copolymer brush for resistivity study
title_sort fabrication of device with poly(n-isopropylacrylamide)-b-ssdna copolymer brush for resistivity study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5629771/
https://www.ncbi.nlm.nih.gov/pubmed/28982368
http://dx.doi.org/10.1186/s12951-017-0303-4
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