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Development of Specific Monoclonal Antibodies against Porcine RIG-I-like Receptors Revealed the Species Specificity
The RIG-I-like receptors (RLRs) play critical roles in sensing and combating viral infections, particularly RNA virus infections. However, there is a dearth of research on livestock RLRs due to a lack of specific antibodies. In this study, we purified porcine RLR proteins and developed monoclonal an...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9967608/ https://www.ncbi.nlm.nih.gov/pubmed/36835527 http://dx.doi.org/10.3390/ijms24044118 |
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author | Shao, Qi Li, Shuangjie Cao, Qi Gu, Haotian Zhang, Jiajia Zhang, Youwen Zhang, Kaili Zheng, Wanglong Chen, Nanhua Shang, Shaobin Zhu, Jianzhong |
author_facet | Shao, Qi Li, Shuangjie Cao, Qi Gu, Haotian Zhang, Jiajia Zhang, Youwen Zhang, Kaili Zheng, Wanglong Chen, Nanhua Shang, Shaobin Zhu, Jianzhong |
author_sort | Shao, Qi |
collection | PubMed |
description | The RIG-I-like receptors (RLRs) play critical roles in sensing and combating viral infections, particularly RNA virus infections. However, there is a dearth of research on livestock RLRs due to a lack of specific antibodies. In this study, we purified porcine RLR proteins and developed monoclonal antibodies (mAbs) against porcine RLR members RIG-I, MDA5 and LGP2, for which one, one and two hybridomas were obtained, respectively. The porcine RIG-I and MDA5 mAbs each targeted the regions beyond the N-terminal CARDs domains, whereas the two LGP2 mAbs were both directed to the N-terminal helicase ATP binding domain in the Western blotting. In addition, all of the porcine RLR mAbs recognized the corresponding cytoplasmic RLR proteins in the immunofluorescence and immunochemistry assays. Importantly, both RIG-I and MDA5 mAbs are porcine specific, without demonstrating any cross-reactions with the human counterparts. As for the two LGP2 mAbs, one is porcine specific, whereas another one reacts with both porcine and human LGP2. Thus, our study not only provides useful tools for porcine RLR antiviral signaling research, but also reveals the porcine species specificity, giving significant insights into porcine innate immunity and immune biology. |
format | Online Article Text |
id | pubmed-9967608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99676082023-02-27 Development of Specific Monoclonal Antibodies against Porcine RIG-I-like Receptors Revealed the Species Specificity Shao, Qi Li, Shuangjie Cao, Qi Gu, Haotian Zhang, Jiajia Zhang, Youwen Zhang, Kaili Zheng, Wanglong Chen, Nanhua Shang, Shaobin Zhu, Jianzhong Int J Mol Sci Article The RIG-I-like receptors (RLRs) play critical roles in sensing and combating viral infections, particularly RNA virus infections. However, there is a dearth of research on livestock RLRs due to a lack of specific antibodies. In this study, we purified porcine RLR proteins and developed monoclonal antibodies (mAbs) against porcine RLR members RIG-I, MDA5 and LGP2, for which one, one and two hybridomas were obtained, respectively. The porcine RIG-I and MDA5 mAbs each targeted the regions beyond the N-terminal CARDs domains, whereas the two LGP2 mAbs were both directed to the N-terminal helicase ATP binding domain in the Western blotting. In addition, all of the porcine RLR mAbs recognized the corresponding cytoplasmic RLR proteins in the immunofluorescence and immunochemistry assays. Importantly, both RIG-I and MDA5 mAbs are porcine specific, without demonstrating any cross-reactions with the human counterparts. As for the two LGP2 mAbs, one is porcine specific, whereas another one reacts with both porcine and human LGP2. Thus, our study not only provides useful tools for porcine RLR antiviral signaling research, but also reveals the porcine species specificity, giving significant insights into porcine innate immunity and immune biology. MDPI 2023-02-18 /pmc/articles/PMC9967608/ /pubmed/36835527 http://dx.doi.org/10.3390/ijms24044118 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Shao, Qi Li, Shuangjie Cao, Qi Gu, Haotian Zhang, Jiajia Zhang, Youwen Zhang, Kaili Zheng, Wanglong Chen, Nanhua Shang, Shaobin Zhu, Jianzhong Development of Specific Monoclonal Antibodies against Porcine RIG-I-like Receptors Revealed the Species Specificity |
title | Development of Specific Monoclonal Antibodies against Porcine RIG-I-like Receptors Revealed the Species Specificity |
title_full | Development of Specific Monoclonal Antibodies against Porcine RIG-I-like Receptors Revealed the Species Specificity |
title_fullStr | Development of Specific Monoclonal Antibodies against Porcine RIG-I-like Receptors Revealed the Species Specificity |
title_full_unstemmed | Development of Specific Monoclonal Antibodies against Porcine RIG-I-like Receptors Revealed the Species Specificity |
title_short | Development of Specific Monoclonal Antibodies against Porcine RIG-I-like Receptors Revealed the Species Specificity |
title_sort | development of specific monoclonal antibodies against porcine rig-i-like receptors revealed the species specificity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9967608/ https://www.ncbi.nlm.nih.gov/pubmed/36835527 http://dx.doi.org/10.3390/ijms24044118 |
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