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Production and characterization of a recombinant single-chain antibody against Hantaan virus envelop glycoprotein
Hantaan virus (HTNV) is the type of Hantavirus causing hemorrhagic fever with renal syndrome, for which no specific therapeutics are available so far. Cell type-specific internalizing antibodies can be used to deliver therapeutics intracellularly to target cell and thus, have potential application i...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Springer-Verlag
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2844961/ https://www.ncbi.nlm.nih.gov/pubmed/20012277 http://dx.doi.org/10.1007/s00253-009-2379-8 |
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author | Yang, Jie Chen, Rui Wei, Junxia Zhang, Fanglin Zhang, Yong Jia, Lintao Yan, Yan Luo, Wen Cao, Yunxin Yao, Libo Sun, Jifeng Xu, Zhikai Yang, Angang |
author_facet | Yang, Jie Chen, Rui Wei, Junxia Zhang, Fanglin Zhang, Yong Jia, Lintao Yan, Yan Luo, Wen Cao, Yunxin Yao, Libo Sun, Jifeng Xu, Zhikai Yang, Angang |
author_sort | Yang, Jie |
collection | PubMed |
description | Hantaan virus (HTNV) is the type of Hantavirus causing hemorrhagic fever with renal syndrome, for which no specific therapeutics are available so far. Cell type-specific internalizing antibodies can be used to deliver therapeutics intracellularly to target cell and thus, have potential application in anti-HTNV infection. To achieve intracellular delivery of therapeutics, it is necessary to obtain antibodies that demonstrate sufficient cell type-specific binding, internalizing, and desired cellular trafficking. Here, we describe the prokaryotic expression, affinity purification, and functional testing of a single-chain Fv antibody fragment (scFv) against HTNV envelop glycoprotein (GP), an HTNV-specific antigen normally located on the membranes of HTNV-infected cells. This HTNV GP-targeting antibody, scFv3G1, was produced in the cytoplasm of Escherichia coli cells as a soluble protein and was purified by immobilized metal affinity chromatography. The purified scFv possessed a high specific antigen-binding activity to HTNV GP and HTNV-infected Vero E6 cells and could be internalized into HTNV-infected cells probably through the clathrin-dependent endocytosis pathways similar to that observed with transferrin. Our results showed that the E. coli-produced scFv had potential applications in targeted and intracellular delivery of therapeutics against HTNV infections. |
format | Text |
id | pubmed-2844961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-28449612010-04-05 Production and characterization of a recombinant single-chain antibody against Hantaan virus envelop glycoprotein Yang, Jie Chen, Rui Wei, Junxia Zhang, Fanglin Zhang, Yong Jia, Lintao Yan, Yan Luo, Wen Cao, Yunxin Yao, Libo Sun, Jifeng Xu, Zhikai Yang, Angang Appl Microbiol Biotechnol Biotechnological Products and Process Engineering Hantaan virus (HTNV) is the type of Hantavirus causing hemorrhagic fever with renal syndrome, for which no specific therapeutics are available so far. Cell type-specific internalizing antibodies can be used to deliver therapeutics intracellularly to target cell and thus, have potential application in anti-HTNV infection. To achieve intracellular delivery of therapeutics, it is necessary to obtain antibodies that demonstrate sufficient cell type-specific binding, internalizing, and desired cellular trafficking. Here, we describe the prokaryotic expression, affinity purification, and functional testing of a single-chain Fv antibody fragment (scFv) against HTNV envelop glycoprotein (GP), an HTNV-specific antigen normally located on the membranes of HTNV-infected cells. This HTNV GP-targeting antibody, scFv3G1, was produced in the cytoplasm of Escherichia coli cells as a soluble protein and was purified by immobilized metal affinity chromatography. The purified scFv possessed a high specific antigen-binding activity to HTNV GP and HTNV-infected Vero E6 cells and could be internalized into HTNV-infected cells probably through the clathrin-dependent endocytosis pathways similar to that observed with transferrin. Our results showed that the E. coli-produced scFv had potential applications in targeted and intracellular delivery of therapeutics against HTNV infections. Springer-Verlag 2009-12-10 2010 /pmc/articles/PMC2844961/ /pubmed/20012277 http://dx.doi.org/10.1007/s00253-009-2379-8 Text en © The Author(s) 2009 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Biotechnological Products and Process Engineering Yang, Jie Chen, Rui Wei, Junxia Zhang, Fanglin Zhang, Yong Jia, Lintao Yan, Yan Luo, Wen Cao, Yunxin Yao, Libo Sun, Jifeng Xu, Zhikai Yang, Angang Production and characterization of a recombinant single-chain antibody against Hantaan virus envelop glycoprotein |
title | Production and characterization of a recombinant single-chain antibody against Hantaan virus envelop glycoprotein |
title_full | Production and characterization of a recombinant single-chain antibody against Hantaan virus envelop glycoprotein |
title_fullStr | Production and characterization of a recombinant single-chain antibody against Hantaan virus envelop glycoprotein |
title_full_unstemmed | Production and characterization of a recombinant single-chain antibody against Hantaan virus envelop glycoprotein |
title_short | Production and characterization of a recombinant single-chain antibody against Hantaan virus envelop glycoprotein |
title_sort | production and characterization of a recombinant single-chain antibody against hantaan virus envelop glycoprotein |
topic | Biotechnological Products and Process Engineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2844961/ https://www.ncbi.nlm.nih.gov/pubmed/20012277 http://dx.doi.org/10.1007/s00253-009-2379-8 |
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