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Atomic Force Microscopy Study of the Effect of an Electric Field, Applied to a Pyramidal Structure, on Enzyme Biomolecules

The influence of an external constant strong electric field, formed using a pyramidal structure under a high electric potential, on an enzyme located near its apex, is studied. Horseradish peroxidase (HRP) is used as a model. In our experiments, a 27 kV direct current (DC) voltage was applied to two...

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Autores principales: Ivanov, Yuri D., Tatur, Vadim Y., Shumov, Ivan D., Kozlov, Andrey F., Valueva, Anastasia A., Ivanova, Irina A., Ershova, Maria O., Ivanova, Nina D., Stepanov, Igor N., Lukyanitsa, Andrei A., Ziborov, Vadim S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9680214/
https://www.ncbi.nlm.nih.gov/pubmed/36412875
http://dx.doi.org/10.3390/jfb13040234
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author Ivanov, Yuri D.
Tatur, Vadim Y.
Shumov, Ivan D.
Kozlov, Andrey F.
Valueva, Anastasia A.
Ivanova, Irina A.
Ershova, Maria O.
Ivanova, Nina D.
Stepanov, Igor N.
Lukyanitsa, Andrei A.
Ziborov, Vadim S.
author_facet Ivanov, Yuri D.
Tatur, Vadim Y.
Shumov, Ivan D.
Kozlov, Andrey F.
Valueva, Anastasia A.
Ivanova, Irina A.
Ershova, Maria O.
Ivanova, Nina D.
Stepanov, Igor N.
Lukyanitsa, Andrei A.
Ziborov, Vadim S.
author_sort Ivanov, Yuri D.
collection PubMed
description The influence of an external constant strong electric field, formed using a pyramidal structure under a high electric potential, on an enzyme located near its apex, is studied. Horseradish peroxidase (HRP) is used as a model. In our experiments, a 27 kV direct current (DC) voltage was applied to two electrodes with a conducting pyramidal structure attached to one of them. The enzyme particles were visualized by atomic force microscopy (AFM) after the adsorption of the enzyme from its 0.1 µM solution onto mica AFM substrates. It is demonstrated that after the 40 min exposure to the electric field, the enzyme forms extended structures on mica, while in control experiments compact HRP particles are observed. After the exposure to the electric field, the majority of mica-adsorbed HRP particles had a height of 1.2 nm (as opposed to 1.0 nm in the case of control experiments), and the contribution of higher (>2.0 nm) particles was also considerable. This indicates the formation of high-order HRP aggregates under the influence of an applied electric field. At that, the enzymatic activity of HRP against its substrate 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonate) (ABTS) remains unaffected. These results are important for studying macroscopic effects of strong electromagnetic fields on enzymes, as well as for the development of cellular structure models.
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spelling pubmed-96802142022-11-23 Atomic Force Microscopy Study of the Effect of an Electric Field, Applied to a Pyramidal Structure, on Enzyme Biomolecules Ivanov, Yuri D. Tatur, Vadim Y. Shumov, Ivan D. Kozlov, Andrey F. Valueva, Anastasia A. Ivanova, Irina A. Ershova, Maria O. Ivanova, Nina D. Stepanov, Igor N. Lukyanitsa, Andrei A. Ziborov, Vadim S. J Funct Biomater Communication The influence of an external constant strong electric field, formed using a pyramidal structure under a high electric potential, on an enzyme located near its apex, is studied. Horseradish peroxidase (HRP) is used as a model. In our experiments, a 27 kV direct current (DC) voltage was applied to two electrodes with a conducting pyramidal structure attached to one of them. The enzyme particles were visualized by atomic force microscopy (AFM) after the adsorption of the enzyme from its 0.1 µM solution onto mica AFM substrates. It is demonstrated that after the 40 min exposure to the electric field, the enzyme forms extended structures on mica, while in control experiments compact HRP particles are observed. After the exposure to the electric field, the majority of mica-adsorbed HRP particles had a height of 1.2 nm (as opposed to 1.0 nm in the case of control experiments), and the contribution of higher (>2.0 nm) particles was also considerable. This indicates the formation of high-order HRP aggregates under the influence of an applied electric field. At that, the enzymatic activity of HRP against its substrate 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonate) (ABTS) remains unaffected. These results are important for studying macroscopic effects of strong electromagnetic fields on enzymes, as well as for the development of cellular structure models. MDPI 2022-11-10 /pmc/articles/PMC9680214/ /pubmed/36412875 http://dx.doi.org/10.3390/jfb13040234 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Ivanov, Yuri D.
Tatur, Vadim Y.
Shumov, Ivan D.
Kozlov, Andrey F.
Valueva, Anastasia A.
Ivanova, Irina A.
Ershova, Maria O.
Ivanova, Nina D.
Stepanov, Igor N.
Lukyanitsa, Andrei A.
Ziborov, Vadim S.
Atomic Force Microscopy Study of the Effect of an Electric Field, Applied to a Pyramidal Structure, on Enzyme Biomolecules
title Atomic Force Microscopy Study of the Effect of an Electric Field, Applied to a Pyramidal Structure, on Enzyme Biomolecules
title_full Atomic Force Microscopy Study of the Effect of an Electric Field, Applied to a Pyramidal Structure, on Enzyme Biomolecules
title_fullStr Atomic Force Microscopy Study of the Effect of an Electric Field, Applied to a Pyramidal Structure, on Enzyme Biomolecules
title_full_unstemmed Atomic Force Microscopy Study of the Effect of an Electric Field, Applied to a Pyramidal Structure, on Enzyme Biomolecules
title_short Atomic Force Microscopy Study of the Effect of an Electric Field, Applied to a Pyramidal Structure, on Enzyme Biomolecules
title_sort atomic force microscopy study of the effect of an electric field, applied to a pyramidal structure, on enzyme biomolecules
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9680214/
https://www.ncbi.nlm.nih.gov/pubmed/36412875
http://dx.doi.org/10.3390/jfb13040234
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