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Cloning and identification of the CTLA-4IgV gene and functional application of vaccine in Xinjiang sheep

Cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) is an important surface molecule of activated T cells that has a strong affinity with the B7 molecule on the surface of antigen-presenting cells. Among these molecules, the CTLA-4 extracellular region (CTLA-4 IgV) may be used as a novel immune adj...

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Autores principales: Kong, Huifang, Zhao, Shangqi, Zheng, Jia, Liu, Bin, Zhou, Yanxia, Li, Yanmin, Zhou, Wentao, Zhou, Xiaotao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684741/
https://www.ncbi.nlm.nih.gov/pubmed/36474703
http://dx.doi.org/10.1515/biol-2022-0524
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author Kong, Huifang
Zhao, Shangqi
Zheng, Jia
Liu, Bin
Zhou, Yanxia
Li, Yanmin
Zhou, Wentao
Zhou, Xiaotao
author_facet Kong, Huifang
Zhao, Shangqi
Zheng, Jia
Liu, Bin
Zhou, Yanxia
Li, Yanmin
Zhou, Wentao
Zhou, Xiaotao
author_sort Kong, Huifang
collection PubMed
description Cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) is an important surface molecule of activated T cells that has a strong affinity with the B7 molecule on the surface of antigen-presenting cells. Among these molecules, the CTLA-4 extracellular region (CTLA-4 IgV) may be used as a novel immune adjuvant molecule for delivering antigens and inducing strong humoral and cellular immune responses. In this study, bioinformatics analysis was performed to determine and clone the extracellular region of Xinjiang sheep CTLA-4 (NM_001009214). The CTLA-4 IgV gene was amplified and ligated into the pMD19-T vector, and the positive bacteria were screened by blue-white spots for sequencing and comparison. The correctly sequenced CTLA-4 IgV was digested and then ligated into the prokaryotic expression vector pET-30a(+). The plasmid pET30a–CTLA-4 IgV was constructed to induce the expression of the recombinant protein CTLA-4 IgV. Thereafter, CTLA-4 IgV was identified. Clustal X multiple sequence alignment revealed that the protein sequence of Xinjiang sheep CTLA-4 IgV was different from that of the known CTLA-4 extracellular region. The 3D protein structure of Xinjiang sheep CTLA-4 IgV was constructed via the bioinformatics method. Subsequently, molecular docking between the Xinjiang sheep CTLA-4 IgV protein and the B7 molecule was conducted. Results revealed multiple binding sites in the extracellular region of Xinjiang sheep CTLA-4, and two multiple interactions ensured stable binding after docking. The functionality of the Xinjiang sheep CTLA-4 IgV protein was further verified by fusing the CTLA-4 extracellular V region with EgG1Y162, a protective protein from Echinococcus granulosa, and the purified recombinant protein CTLA-4 IgV–EgG1Y162 was expressed with the mouse bone marrow-derived. The addition of the Xinjiang sheep CTLA-4 IgV protein at the amino terminus promoted the binding of EgG1Y162 to dendritic cells (DCs) and increased the maturation rate of these cells, further indicating that the protein could effectively improve the antigen presentation ability of DCs. The CTLA-4 extracellular domain protein of Xinjiang sheep is unique and has the potential to promote the presentation of the fusion protein by DCs as an adjuvant. The cloning and expression of this gene provide new measures and ideas for the preparation of the Xinjiang sheep vaccine to prevent zoonotic diseases.
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spelling pubmed-96847412022-12-05 Cloning and identification of the CTLA-4IgV gene and functional application of vaccine in Xinjiang sheep Kong, Huifang Zhao, Shangqi Zheng, Jia Liu, Bin Zhou, Yanxia Li, Yanmin Zhou, Wentao Zhou, Xiaotao Open Life Sci Research Article Cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) is an important surface molecule of activated T cells that has a strong affinity with the B7 molecule on the surface of antigen-presenting cells. Among these molecules, the CTLA-4 extracellular region (CTLA-4 IgV) may be used as a novel immune adjuvant molecule for delivering antigens and inducing strong humoral and cellular immune responses. In this study, bioinformatics analysis was performed to determine and clone the extracellular region of Xinjiang sheep CTLA-4 (NM_001009214). The CTLA-4 IgV gene was amplified and ligated into the pMD19-T vector, and the positive bacteria were screened by blue-white spots for sequencing and comparison. The correctly sequenced CTLA-4 IgV was digested and then ligated into the prokaryotic expression vector pET-30a(+). The plasmid pET30a–CTLA-4 IgV was constructed to induce the expression of the recombinant protein CTLA-4 IgV. Thereafter, CTLA-4 IgV was identified. Clustal X multiple sequence alignment revealed that the protein sequence of Xinjiang sheep CTLA-4 IgV was different from that of the known CTLA-4 extracellular region. The 3D protein structure of Xinjiang sheep CTLA-4 IgV was constructed via the bioinformatics method. Subsequently, molecular docking between the Xinjiang sheep CTLA-4 IgV protein and the B7 molecule was conducted. Results revealed multiple binding sites in the extracellular region of Xinjiang sheep CTLA-4, and two multiple interactions ensured stable binding after docking. The functionality of the Xinjiang sheep CTLA-4 IgV protein was further verified by fusing the CTLA-4 extracellular V region with EgG1Y162, a protective protein from Echinococcus granulosa, and the purified recombinant protein CTLA-4 IgV–EgG1Y162 was expressed with the mouse bone marrow-derived. The addition of the Xinjiang sheep CTLA-4 IgV protein at the amino terminus promoted the binding of EgG1Y162 to dendritic cells (DCs) and increased the maturation rate of these cells, further indicating that the protein could effectively improve the antigen presentation ability of DCs. The CTLA-4 extracellular domain protein of Xinjiang sheep is unique and has the potential to promote the presentation of the fusion protein by DCs as an adjuvant. The cloning and expression of this gene provide new measures and ideas for the preparation of the Xinjiang sheep vaccine to prevent zoonotic diseases. De Gruyter 2022-11-23 /pmc/articles/PMC9684741/ /pubmed/36474703 http://dx.doi.org/10.1515/biol-2022-0524 Text en © 2022 the author(s), published by De Gruyter https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License.
spellingShingle Research Article
Kong, Huifang
Zhao, Shangqi
Zheng, Jia
Liu, Bin
Zhou, Yanxia
Li, Yanmin
Zhou, Wentao
Zhou, Xiaotao
Cloning and identification of the CTLA-4IgV gene and functional application of vaccine in Xinjiang sheep
title Cloning and identification of the CTLA-4IgV gene and functional application of vaccine in Xinjiang sheep
title_full Cloning and identification of the CTLA-4IgV gene and functional application of vaccine in Xinjiang sheep
title_fullStr Cloning and identification of the CTLA-4IgV gene and functional application of vaccine in Xinjiang sheep
title_full_unstemmed Cloning and identification of the CTLA-4IgV gene and functional application of vaccine in Xinjiang sheep
title_short Cloning and identification of the CTLA-4IgV gene and functional application of vaccine in Xinjiang sheep
title_sort cloning and identification of the ctla-4igv gene and functional application of vaccine in xinjiang sheep
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684741/
https://www.ncbi.nlm.nih.gov/pubmed/36474703
http://dx.doi.org/10.1515/biol-2022-0524
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