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A New Method for Immobilization of His-Tagged Proteins with the Application of Low-Frequency AC Electric Field
Continued advancement of protein array, bioelectrode, and biosensor technologies is necessary to develop methods for higher amount and highly oriented immobilization activity of proteins. In pursuit of these goals, we developed a new immobilization method by combining electrostatic transport and sub...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876589/ https://www.ncbi.nlm.nih.gov/pubmed/29510585 http://dx.doi.org/10.3390/s18030784 |
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author | Takahashi, Shunsuke Kishi, Kazuki Hiraga, Ryota Hayashi, Kazuki Mamada, Youhei Oshige, Masahiko Katsura, Shinji |
author_facet | Takahashi, Shunsuke Kishi, Kazuki Hiraga, Ryota Hayashi, Kazuki Mamada, Youhei Oshige, Masahiko Katsura, Shinji |
author_sort | Takahashi, Shunsuke |
collection | PubMed |
description | Continued advancement of protein array, bioelectrode, and biosensor technologies is necessary to develop methods for higher amount and highly oriented immobilization activity of proteins. In pursuit of these goals, we developed a new immobilization method by combining electrostatic transport and subsequent molecular diffusion of protein molecules. Our developed immobilization method is based on a model that transports proteins toward the substrate surface due to steep concentration gradient generated by low-frequency AC electric field. The immobilization of the maximum amounts can be obtained by the application of the AC voltage of 80 Vpp, 20 Hz both for His-tagged Green Fluorescent Protein (GFP) and Discosoma sp. Red Fluorescent Protein (DsRed), used as model proteins. The amounts of the immobilized His-tagged GFP and DsRed were approximately seven-fold higher than that in the absence of the application of low-frequency AC electric field. Furthermore, the positively and negatively charged His-tagged GFP at acidic and alkaline pH were immobilized by applying of low-frequency AC electric field, whereas the non-charged His-tagged GFP at the pH corresponding to its isoelectric point (pI) was not immobilized. Therefore, unless the pH is equal to pI, the immobilization of electrically charged proteins was strongly enhanced through electrostatic transport and subsequent molecular diffusion. |
format | Online Article Text |
id | pubmed-5876589 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-58765892018-04-09 A New Method for Immobilization of His-Tagged Proteins with the Application of Low-Frequency AC Electric Field Takahashi, Shunsuke Kishi, Kazuki Hiraga, Ryota Hayashi, Kazuki Mamada, Youhei Oshige, Masahiko Katsura, Shinji Sensors (Basel) Article Continued advancement of protein array, bioelectrode, and biosensor technologies is necessary to develop methods for higher amount and highly oriented immobilization activity of proteins. In pursuit of these goals, we developed a new immobilization method by combining electrostatic transport and subsequent molecular diffusion of protein molecules. Our developed immobilization method is based on a model that transports proteins toward the substrate surface due to steep concentration gradient generated by low-frequency AC electric field. The immobilization of the maximum amounts can be obtained by the application of the AC voltage of 80 Vpp, 20 Hz both for His-tagged Green Fluorescent Protein (GFP) and Discosoma sp. Red Fluorescent Protein (DsRed), used as model proteins. The amounts of the immobilized His-tagged GFP and DsRed were approximately seven-fold higher than that in the absence of the application of low-frequency AC electric field. Furthermore, the positively and negatively charged His-tagged GFP at acidic and alkaline pH were immobilized by applying of low-frequency AC electric field, whereas the non-charged His-tagged GFP at the pH corresponding to its isoelectric point (pI) was not immobilized. Therefore, unless the pH is equal to pI, the immobilization of electrically charged proteins was strongly enhanced through electrostatic transport and subsequent molecular diffusion. MDPI 2018-03-05 /pmc/articles/PMC5876589/ /pubmed/29510585 http://dx.doi.org/10.3390/s18030784 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Takahashi, Shunsuke Kishi, Kazuki Hiraga, Ryota Hayashi, Kazuki Mamada, Youhei Oshige, Masahiko Katsura, Shinji A New Method for Immobilization of His-Tagged Proteins with the Application of Low-Frequency AC Electric Field |
title | A New Method for Immobilization of His-Tagged Proteins with the Application of Low-Frequency AC Electric Field |
title_full | A New Method for Immobilization of His-Tagged Proteins with the Application of Low-Frequency AC Electric Field |
title_fullStr | A New Method for Immobilization of His-Tagged Proteins with the Application of Low-Frequency AC Electric Field |
title_full_unstemmed | A New Method for Immobilization of His-Tagged Proteins with the Application of Low-Frequency AC Electric Field |
title_short | A New Method for Immobilization of His-Tagged Proteins with the Application of Low-Frequency AC Electric Field |
title_sort | new method for immobilization of his-tagged proteins with the application of low-frequency ac electric field |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876589/ https://www.ncbi.nlm.nih.gov/pubmed/29510585 http://dx.doi.org/10.3390/s18030784 |
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