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A surface protein−imprinted biosensor based on boronate affinity for the detection of anti−human immunoglobulin G
A surface protein-imprinted biosensor was constructed on a screen-printed carbon electrode (SPCE) for the detection of anti-human immunoglobulin G (anti-IgG). The SPCE was successively decorated with aminated graphene (NH(2)-G) and gold nanobipyramids (AuNBs) for signal amplification. Then 4-mercapt...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8853174/ https://www.ncbi.nlm.nih.gov/pubmed/35166940 http://dx.doi.org/10.1007/s00604-022-05204-w |
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author | Liu, Zixuan Yin, Zheng-Zhi Cai, Wenrong Wu, Datong Li, Junyao Kong, Yong |
author_facet | Liu, Zixuan Yin, Zheng-Zhi Cai, Wenrong Wu, Datong Li, Junyao Kong, Yong |
author_sort | Liu, Zixuan |
collection | PubMed |
description | A surface protein-imprinted biosensor was constructed on a screen-printed carbon electrode (SPCE) for the detection of anti-human immunoglobulin G (anti-IgG). The SPCE was successively decorated with aminated graphene (NH(2)-G) and gold nanobipyramids (AuNBs) for signal amplification. Then 4-mercaptophenylboric acid (4-MPBA) was covalently anchored to the surface of AuNBs for capturing anti-IgG template through boronate affinity binding. The decorated SPCE was then deposited with an imprinting layer generated by the electropolymerization of pyrrole. After removal of the anti-IgG template by the dissociation of the boronate ester in an acidic solution, three-dimensional (3D) cavities complementary to the anti-IgG template were formed in the imprinting layer of polypyrrole (PPy). The molecularly imprinted polymers (MIP)-based biosensor was used for the detection of anti-IgG, exhibiting a wide linear range from 0.05 to 100 ng mL(−1) and a low limit of detection of 0.017 ng mL(−1) (S/N = 3). In addition, the MIP-based anti-IgG biosensor also shows high selectivity, reproducibility and stability. Finally, the practicability of the fabricated anti-IgG biosensor was demonstrated by accurate determination of anti-IgG in serum sample. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00604-022-05204-w. |
format | Online Article Text |
id | pubmed-8853174 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-88531742022-02-18 A surface protein−imprinted biosensor based on boronate affinity for the detection of anti−human immunoglobulin G Liu, Zixuan Yin, Zheng-Zhi Cai, Wenrong Wu, Datong Li, Junyao Kong, Yong Mikrochim Acta Original Paper A surface protein-imprinted biosensor was constructed on a screen-printed carbon electrode (SPCE) for the detection of anti-human immunoglobulin G (anti-IgG). The SPCE was successively decorated with aminated graphene (NH(2)-G) and gold nanobipyramids (AuNBs) for signal amplification. Then 4-mercaptophenylboric acid (4-MPBA) was covalently anchored to the surface of AuNBs for capturing anti-IgG template through boronate affinity binding. The decorated SPCE was then deposited with an imprinting layer generated by the electropolymerization of pyrrole. After removal of the anti-IgG template by the dissociation of the boronate ester in an acidic solution, three-dimensional (3D) cavities complementary to the anti-IgG template were formed in the imprinting layer of polypyrrole (PPy). The molecularly imprinted polymers (MIP)-based biosensor was used for the detection of anti-IgG, exhibiting a wide linear range from 0.05 to 100 ng mL(−1) and a low limit of detection of 0.017 ng mL(−1) (S/N = 3). In addition, the MIP-based anti-IgG biosensor also shows high selectivity, reproducibility and stability. Finally, the practicability of the fabricated anti-IgG biosensor was demonstrated by accurate determination of anti-IgG in serum sample. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00604-022-05204-w. Springer Vienna 2022-02-15 2022 /pmc/articles/PMC8853174/ /pubmed/35166940 http://dx.doi.org/10.1007/s00604-022-05204-w Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Paper Liu, Zixuan Yin, Zheng-Zhi Cai, Wenrong Wu, Datong Li, Junyao Kong, Yong A surface protein−imprinted biosensor based on boronate affinity for the detection of anti−human immunoglobulin G |
title | A surface protein−imprinted biosensor based on boronate affinity for the detection of anti−human immunoglobulin G |
title_full | A surface protein−imprinted biosensor based on boronate affinity for the detection of anti−human immunoglobulin G |
title_fullStr | A surface protein−imprinted biosensor based on boronate affinity for the detection of anti−human immunoglobulin G |
title_full_unstemmed | A surface protein−imprinted biosensor based on boronate affinity for the detection of anti−human immunoglobulin G |
title_short | A surface protein−imprinted biosensor based on boronate affinity for the detection of anti−human immunoglobulin G |
title_sort | surface protein−imprinted biosensor based on boronate affinity for the detection of anti−human immunoglobulin g |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8853174/ https://www.ncbi.nlm.nih.gov/pubmed/35166940 http://dx.doi.org/10.1007/s00604-022-05204-w |
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