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Development of novel-nanobody-based lateral-flow immunochromatographic strip test for rapid detection of recombinant human interferon α2b

Recombinant human interferon α2b (rhIFNα2b) is widely used as an antiviral therapy agent for the treatment of hepatitis B and hepatitis C. The current identification test for rhIFNα2b is complex. In this study, an anti-rhIFNα2b nanobody was discovered and used for the development of a rapid lateral...

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Autores principales: Qin, Xi, Duan, Maoqin, Pei, Dening, Lin, Jian, Wang, Lan, Zhou, Peng, Yao, Wenrong, Guo, Ying, Li, Xiang, Tao, Lei, Ding, Youxue, Liu, Lan, Zhou, Yong, Jia, Chuncui, Rao, Chunming, Wang, Junzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Xi'an Jiaotong University 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9091920/
https://www.ncbi.nlm.nih.gov/pubmed/35582401
http://dx.doi.org/10.1016/j.jpha.2021.07.003
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author Qin, Xi
Duan, Maoqin
Pei, Dening
Lin, Jian
Wang, Lan
Zhou, Peng
Yao, Wenrong
Guo, Ying
Li, Xiang
Tao, Lei
Ding, Youxue
Liu, Lan
Zhou, Yong
Jia, Chuncui
Rao, Chunming
Wang, Junzhi
author_facet Qin, Xi
Duan, Maoqin
Pei, Dening
Lin, Jian
Wang, Lan
Zhou, Peng
Yao, Wenrong
Guo, Ying
Li, Xiang
Tao, Lei
Ding, Youxue
Liu, Lan
Zhou, Yong
Jia, Chuncui
Rao, Chunming
Wang, Junzhi
author_sort Qin, Xi
collection PubMed
description Recombinant human interferon α2b (rhIFNα2b) is widely used as an antiviral therapy agent for the treatment of hepatitis B and hepatitis C. The current identification test for rhIFNα2b is complex. In this study, an anti-rhIFNα2b nanobody was discovered and used for the development of a rapid lateral flow strip for the identification of rhIFNα2b. RhIFNα2b was used to immunize an alpaca, which established a phage nanobody library. After five steps of enrichment, the nanobody I22, which specifically bound rhIFNα2b, was isolated and inserted into the prokaryotic expression vector pET28a. After subsequent purification, the physicochemical properties of the nanobody were determined. A semiquantitative detection and rapid identification assay of rhIFNα2b was developed using this novel nanobody. To develop a rapid test, the nanobody I22 was coupled with a colloidal gold to produce lateral-flow test strips. The developed rhIFNα2b detection assay had a limit of detection of 1 μg/mL. The isolation of I22 and successful construction of a lateral-flow immunochromatographic test strip demonstrated the feasibility of performing ligand-binding assays on a lateral-flow test strip using recombinant protein products. The principle of this novel assay is generally applicable for the rapid testing of other commercial products, with a great potential for routine use in detecting counterfeit recombinant protein products.
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spelling pubmed-90919202022-05-16 Development of novel-nanobody-based lateral-flow immunochromatographic strip test for rapid detection of recombinant human interferon α2b Qin, Xi Duan, Maoqin Pei, Dening Lin, Jian Wang, Lan Zhou, Peng Yao, Wenrong Guo, Ying Li, Xiang Tao, Lei Ding, Youxue Liu, Lan Zhou, Yong Jia, Chuncui Rao, Chunming Wang, Junzhi J Pharm Anal Original Article Recombinant human interferon α2b (rhIFNα2b) is widely used as an antiviral therapy agent for the treatment of hepatitis B and hepatitis C. The current identification test for rhIFNα2b is complex. In this study, an anti-rhIFNα2b nanobody was discovered and used for the development of a rapid lateral flow strip for the identification of rhIFNα2b. RhIFNα2b was used to immunize an alpaca, which established a phage nanobody library. After five steps of enrichment, the nanobody I22, which specifically bound rhIFNα2b, was isolated and inserted into the prokaryotic expression vector pET28a. After subsequent purification, the physicochemical properties of the nanobody were determined. A semiquantitative detection and rapid identification assay of rhIFNα2b was developed using this novel nanobody. To develop a rapid test, the nanobody I22 was coupled with a colloidal gold to produce lateral-flow test strips. The developed rhIFNα2b detection assay had a limit of detection of 1 μg/mL. The isolation of I22 and successful construction of a lateral-flow immunochromatographic test strip demonstrated the feasibility of performing ligand-binding assays on a lateral-flow test strip using recombinant protein products. The principle of this novel assay is generally applicable for the rapid testing of other commercial products, with a great potential for routine use in detecting counterfeit recombinant protein products. Xi'an Jiaotong University 2022-04 2021-07-08 /pmc/articles/PMC9091920/ /pubmed/35582401 http://dx.doi.org/10.1016/j.jpha.2021.07.003 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Qin, Xi
Duan, Maoqin
Pei, Dening
Lin, Jian
Wang, Lan
Zhou, Peng
Yao, Wenrong
Guo, Ying
Li, Xiang
Tao, Lei
Ding, Youxue
Liu, Lan
Zhou, Yong
Jia, Chuncui
Rao, Chunming
Wang, Junzhi
Development of novel-nanobody-based lateral-flow immunochromatographic strip test for rapid detection of recombinant human interferon α2b
title Development of novel-nanobody-based lateral-flow immunochromatographic strip test for rapid detection of recombinant human interferon α2b
title_full Development of novel-nanobody-based lateral-flow immunochromatographic strip test for rapid detection of recombinant human interferon α2b
title_fullStr Development of novel-nanobody-based lateral-flow immunochromatographic strip test for rapid detection of recombinant human interferon α2b
title_full_unstemmed Development of novel-nanobody-based lateral-flow immunochromatographic strip test for rapid detection of recombinant human interferon α2b
title_short Development of novel-nanobody-based lateral-flow immunochromatographic strip test for rapid detection of recombinant human interferon α2b
title_sort development of novel-nanobody-based lateral-flow immunochromatographic strip test for rapid detection of recombinant human interferon α2b
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9091920/
https://www.ncbi.nlm.nih.gov/pubmed/35582401
http://dx.doi.org/10.1016/j.jpha.2021.07.003
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