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Starch-Coated Magnetic Iron Oxide Nanoparticles for Affinity Purification of Recombinant Proteins
Starch-coated magnetic iron oxide nanoparticles have been synthesized by a simple, fast, and cost-effective co-precipitation method with cornstarch as a stabilizing agent. The structural and magnetic characteristics of the synthesized material have been studied by transmission electron microscopy, M...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140719/ https://www.ncbi.nlm.nih.gov/pubmed/35628220 http://dx.doi.org/10.3390/ijms23105410 |
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author | Krasitskaya, Vasilisa V. Kudryavtsev, Alexander N. Yaroslavtsev, Roman N. Velikanov, Dmitry A. Bayukov, Oleg A. Gerasimova, Yulia V. Stolyar, Sergey V. Frank, Ludmila A. |
author_facet | Krasitskaya, Vasilisa V. Kudryavtsev, Alexander N. Yaroslavtsev, Roman N. Velikanov, Dmitry A. Bayukov, Oleg A. Gerasimova, Yulia V. Stolyar, Sergey V. Frank, Ludmila A. |
author_sort | Krasitskaya, Vasilisa V. |
collection | PubMed |
description | Starch-coated magnetic iron oxide nanoparticles have been synthesized by a simple, fast, and cost-effective co-precipitation method with cornstarch as a stabilizing agent. The structural and magnetic characteristics of the synthesized material have been studied by transmission electron microscopy, Mössbauer spectroscopy, and vibrating sample magnetometry. The nature of bonds between ferrihydrite nanoparticles and a starch shell has been examined by Fourier transform infrared spectroscopy. The data on the magnetic response of the prepared composite particles have been obtained by magnetic measurements. The determined magnetic characteristics make the synthesized material a good candidate for use in magnetic separation. Starch-coated magnetic iron oxide nanoparticles have been tested as an affinity sorbent for one-step purification of several recombinant proteins (cardiac troponin I, survivin, and melanoma inhibitory activity protein) bearing the maltose-binding protein as an auxiliary fragment. It has been shown that, due to the highly specific binding of this fragment to the starch shell, the target fusion protein is selectively immobilized on magnetic nanoparticles and eluted with the maltose solution. The excellent efficiency of column-free purification, high binding capacity of the sorbent (100–500 µg of a recombinant protein per milligram of starch-coated magnetic iron oxide nanoparticles), and reusability of the obtained material have been demonstrated. |
format | Online Article Text |
id | pubmed-9140719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91407192022-05-28 Starch-Coated Magnetic Iron Oxide Nanoparticles for Affinity Purification of Recombinant Proteins Krasitskaya, Vasilisa V. Kudryavtsev, Alexander N. Yaroslavtsev, Roman N. Velikanov, Dmitry A. Bayukov, Oleg A. Gerasimova, Yulia V. Stolyar, Sergey V. Frank, Ludmila A. Int J Mol Sci Article Starch-coated magnetic iron oxide nanoparticles have been synthesized by a simple, fast, and cost-effective co-precipitation method with cornstarch as a stabilizing agent. The structural and magnetic characteristics of the synthesized material have been studied by transmission electron microscopy, Mössbauer spectroscopy, and vibrating sample magnetometry. The nature of bonds between ferrihydrite nanoparticles and a starch shell has been examined by Fourier transform infrared spectroscopy. The data on the magnetic response of the prepared composite particles have been obtained by magnetic measurements. The determined magnetic characteristics make the synthesized material a good candidate for use in magnetic separation. Starch-coated magnetic iron oxide nanoparticles have been tested as an affinity sorbent for one-step purification of several recombinant proteins (cardiac troponin I, survivin, and melanoma inhibitory activity protein) bearing the maltose-binding protein as an auxiliary fragment. It has been shown that, due to the highly specific binding of this fragment to the starch shell, the target fusion protein is selectively immobilized on magnetic nanoparticles and eluted with the maltose solution. The excellent efficiency of column-free purification, high binding capacity of the sorbent (100–500 µg of a recombinant protein per milligram of starch-coated magnetic iron oxide nanoparticles), and reusability of the obtained material have been demonstrated. MDPI 2022-05-12 /pmc/articles/PMC9140719/ /pubmed/35628220 http://dx.doi.org/10.3390/ijms23105410 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 | Article Krasitskaya, Vasilisa V. Kudryavtsev, Alexander N. Yaroslavtsev, Roman N. Velikanov, Dmitry A. Bayukov, Oleg A. Gerasimova, Yulia V. Stolyar, Sergey V. Frank, Ludmila A. Starch-Coated Magnetic Iron Oxide Nanoparticles for Affinity Purification of Recombinant Proteins |
title | Starch-Coated Magnetic Iron Oxide Nanoparticles for Affinity Purification of Recombinant Proteins |
title_full | Starch-Coated Magnetic Iron Oxide Nanoparticles for Affinity Purification of Recombinant Proteins |
title_fullStr | Starch-Coated Magnetic Iron Oxide Nanoparticles for Affinity Purification of Recombinant Proteins |
title_full_unstemmed | Starch-Coated Magnetic Iron Oxide Nanoparticles for Affinity Purification of Recombinant Proteins |
title_short | Starch-Coated Magnetic Iron Oxide Nanoparticles for Affinity Purification of Recombinant Proteins |
title_sort | starch-coated magnetic iron oxide nanoparticles for affinity purification of recombinant proteins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140719/ https://www.ncbi.nlm.nih.gov/pubmed/35628220 http://dx.doi.org/10.3390/ijms23105410 |
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