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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...

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Autores principales: Takahashi, Shunsuke, Kishi, Kazuki, Hiraga, Ryota, Hayashi, Kazuki, Mamada, Youhei, Oshige, Masahiko, Katsura, Shinji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
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.
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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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