Magnetic Nanoclusters Coated with Albumin, Casein, and Gelatin: Size Tuning, Relaxivity, Stability, Protein Corona, and Application in Nuclear Magnetic Resonance Immunoassay

The surface functionalization of magnetic nanoparticles improves their physicochemical properties and applicability in biomedicine. Natural polymers, including proteins, are prospective coatings capable of increasing the stability, biocompatibility, and transverse relaxivity (r2) of magnetic nanopar...

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Main Authors: Pavel Khramtsov, Irina Barkina, Maria Kropaneva, Maria Bochkova, Valeria Timganova, Anton Nechaev, Il’ya Byzov, Svetlana Zamorina, Anatoly Yermakov, Mikhail Rayev
Format: Article
Language:English
Published: MDPI AG 2019-09-01
Series:Nanomaterials
Subjects:
Online Access:https://www.mdpi.com/2079-4991/9/9/1345
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spelling doaj-50f02f4387df48b7a314f845a0fa7a452020-11-24T21:26:28ZengMDPI AGNanomaterials2079-49912019-09-0199134510.3390/nano9091345nano9091345Magnetic Nanoclusters Coated with Albumin, Casein, and Gelatin: Size Tuning, Relaxivity, Stability, Protein Corona, and Application in Nuclear Magnetic Resonance ImmunoassayPavel Khramtsov0Irina Barkina1Maria Kropaneva2Maria Bochkova3Valeria Timganova4Anton Nechaev5Il’ya Byzov6Svetlana Zamorina7Anatoly Yermakov8Mikhail Rayev9Laboratory of Ecological Immunology, Institute of Ecology and Genetics of Microorganisms of the Ural Branch of the Russian Academy of Sciences, Branch of PSRC UB RAS, 13 Golev str., 614081 Perm, RussiaDepartment of Microbiology and Immunology, Biology Faculty, Perm State National Research University, 15 Bukirev str., 614000 Perm, RussiaLaboratory of Ecological Immunology, Institute of Ecology and Genetics of Microorganisms of the Ural Branch of the Russian Academy of Sciences, Branch of PSRC UB RAS, 13 Golev str., 614081 Perm, RussiaLaboratory of Ecological Immunology, Institute of Ecology and Genetics of Microorganisms of the Ural Branch of the Russian Academy of Sciences, Branch of PSRC UB RAS, 13 Golev str., 614081 Perm, RussiaLaboratory of Ecological Immunology, Institute of Ecology and Genetics of Microorganisms of the Ural Branch of the Russian Academy of Sciences, Branch of PSRC UB RAS, 13 Golev str., 614081 Perm, RussiaInstitute of Technical Chemistry of Ural Branch of the RAS, 3 Academician Korolev str., 614013 Perm, RussiaLaboratory of Ecological Immunology, Institute of Ecology and Genetics of Microorganisms of the Ural Branch of the Russian Academy of Sciences, Branch of PSRC UB RAS, 13 Golev str., 614081 Perm, RussiaLaboratory of Ecological Immunology, Institute of Ecology and Genetics of Microorganisms of the Ural Branch of the Russian Academy of Sciences, Branch of PSRC UB RAS, 13 Golev str., 614081 Perm, RussiaLaboratory of Ecological Immunology, Institute of Ecology and Genetics of Microorganisms of the Ural Branch of the Russian Academy of Sciences, Branch of PSRC UB RAS, 13 Golev str., 614081 Perm, RussiaLaboratory of Ecological Immunology, Institute of Ecology and Genetics of Microorganisms of the Ural Branch of the Russian Academy of Sciences, Branch of PSRC UB RAS, 13 Golev str., 614081 Perm, RussiaThe surface functionalization of magnetic nanoparticles improves their physicochemical properties and applicability in biomedicine. Natural polymers, including proteins, are prospective coatings capable of increasing the stability, biocompatibility, and transverse relaxivity (r2) of magnetic nanoparticles. In this work, we functionalized the nanoclusters of carbon-coated iron nanoparticles with four proteins: bovine serum albumin, casein, and gelatins A and B, and we conducted a comprehensive comparative study of their properties essential to applications in biosensing. First, we examined the influence of environmental parameters on the size of prepared nanoclusters and synthesized protein-coated nanoclusters with a tunable size. Second, we showed that protein coating does not significantly influence the r2 relaxivity of clustered nanoparticles; however, the uniform distribution of individual nanoparticles inside the protein coating facilitates increased relaxivity. Third, we demonstrated the applicability of the obtained nanoclusters in biosensing by the development of a nuclear-magnetic-resonance-based immunoassay for the quantification of antibodies against tetanus toxoid. Fourth, the protein coronas of nanoclusters were studied using SDS-PAGE and Bradford protein assay. Finally, we compared the colloidal stability at various pH values and ionic strengths and in relevant complex media (i.e., blood serum, plasma, milk, juice, beer, and red wine), as well as the heat stability, resistance to proteolytic digestion, and shelf-life of protein-coated nanoclusters.https://www.mdpi.com/2079-4991/9/9/1345nanoparticlesproteinassaycolloidal stabilityantibodyprotein Gstreptavidin
collection DOAJ
language English
format Article
sources DOAJ
author Pavel Khramtsov
Irina Barkina
Maria Kropaneva
Maria Bochkova
Valeria Timganova
Anton Nechaev
Il’ya Byzov
Svetlana Zamorina
Anatoly Yermakov
Mikhail Rayev
spellingShingle Pavel Khramtsov
Irina Barkina
Maria Kropaneva
Maria Bochkova
Valeria Timganova
Anton Nechaev
Il’ya Byzov
Svetlana Zamorina
Anatoly Yermakov
Mikhail Rayev
Magnetic Nanoclusters Coated with Albumin, Casein, and Gelatin: Size Tuning, Relaxivity, Stability, Protein Corona, and Application in Nuclear Magnetic Resonance Immunoassay
Nanomaterials
nanoparticles
protein
assay
colloidal stability
antibody
protein G
streptavidin
author_facet Pavel Khramtsov
Irina Barkina
Maria Kropaneva
Maria Bochkova
Valeria Timganova
Anton Nechaev
Il’ya Byzov
Svetlana Zamorina
Anatoly Yermakov
Mikhail Rayev
author_sort Pavel Khramtsov
title Magnetic Nanoclusters Coated with Albumin, Casein, and Gelatin: Size Tuning, Relaxivity, Stability, Protein Corona, and Application in Nuclear Magnetic Resonance Immunoassay
title_short Magnetic Nanoclusters Coated with Albumin, Casein, and Gelatin: Size Tuning, Relaxivity, Stability, Protein Corona, and Application in Nuclear Magnetic Resonance Immunoassay
title_full Magnetic Nanoclusters Coated with Albumin, Casein, and Gelatin: Size Tuning, Relaxivity, Stability, Protein Corona, and Application in Nuclear Magnetic Resonance Immunoassay
title_fullStr Magnetic Nanoclusters Coated with Albumin, Casein, and Gelatin: Size Tuning, Relaxivity, Stability, Protein Corona, and Application in Nuclear Magnetic Resonance Immunoassay
title_full_unstemmed Magnetic Nanoclusters Coated with Albumin, Casein, and Gelatin: Size Tuning, Relaxivity, Stability, Protein Corona, and Application in Nuclear Magnetic Resonance Immunoassay
title_sort magnetic nanoclusters coated with albumin, casein, and gelatin: size tuning, relaxivity, stability, protein corona, and application in nuclear magnetic resonance immunoassay
publisher MDPI AG
series Nanomaterials
issn 2079-4991
publishDate 2019-09-01
description The surface functionalization of magnetic nanoparticles improves their physicochemical properties and applicability in biomedicine. Natural polymers, including proteins, are prospective coatings capable of increasing the stability, biocompatibility, and transverse relaxivity (r2) of magnetic nanoparticles. In this work, we functionalized the nanoclusters of carbon-coated iron nanoparticles with four proteins: bovine serum albumin, casein, and gelatins A and B, and we conducted a comprehensive comparative study of their properties essential to applications in biosensing. First, we examined the influence of environmental parameters on the size of prepared nanoclusters and synthesized protein-coated nanoclusters with a tunable size. Second, we showed that protein coating does not significantly influence the r2 relaxivity of clustered nanoparticles; however, the uniform distribution of individual nanoparticles inside the protein coating facilitates increased relaxivity. Third, we demonstrated the applicability of the obtained nanoclusters in biosensing by the development of a nuclear-magnetic-resonance-based immunoassay for the quantification of antibodies against tetanus toxoid. Fourth, the protein coronas of nanoclusters were studied using SDS-PAGE and Bradford protein assay. Finally, we compared the colloidal stability at various pH values and ionic strengths and in relevant complex media (i.e., blood serum, plasma, milk, juice, beer, and red wine), as well as the heat stability, resistance to proteolytic digestion, and shelf-life of protein-coated nanoclusters.
topic nanoparticles
protein
assay
colloidal stability
antibody
protein G
streptavidin
url https://www.mdpi.com/2079-4991/9/9/1345
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