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Bamboo Shark as a Small Animal Model for Single Domain Antibody Production

The development of shark single domain antibodies (sdAbs) is hindered by the high cost and tediousness of large-sized shark farming. Here, we demonstrated white-spotted bamboo sharks (Chiloscyllium plagiosum) being cultivated commercially as a promising small animal model to produce sdAbs. We found...

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Autores principales: Wei, Likun, Wang, Meiniang, Xiang, Haitao, Jiang, Yuan, Gong, Jinhua, Su, Dan, Al Azad, M. A. R., Dong, Hongming, Feng, Limin, Wu, Jiajun, Chan, Leo Lai, Yang, Naibo, Shi, Jiahai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8692893/
https://www.ncbi.nlm.nih.gov/pubmed/34957081
http://dx.doi.org/10.3389/fbioe.2021.792111
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author Wei, Likun
Wang, Meiniang
Xiang, Haitao
Jiang, Yuan
Gong, Jinhua
Su, Dan
Al Azad, M. A. R.
Dong, Hongming
Feng, Limin
Wu, Jiajun
Chan, Leo Lai
Yang, Naibo
Shi, Jiahai
author_facet Wei, Likun
Wang, Meiniang
Xiang, Haitao
Jiang, Yuan
Gong, Jinhua
Su, Dan
Al Azad, M. A. R.
Dong, Hongming
Feng, Limin
Wu, Jiajun
Chan, Leo Lai
Yang, Naibo
Shi, Jiahai
author_sort Wei, Likun
collection PubMed
description The development of shark single domain antibodies (sdAbs) is hindered by the high cost and tediousness of large-sized shark farming. Here, we demonstrated white-spotted bamboo sharks (Chiloscyllium plagiosum) being cultivated commercially as a promising small animal model to produce sdAbs. We found that immunoglobulin new antigen receptor (IgNAR) presented in bamboo shark genome, transcriptome, and plasma. Four complete IgNAR clusters including variable domains (vNARs) were discovered in the germline, and the Variable–Joining pair from IgNAR1 cluster was dominant from immune repertoires in blood. Bamboo sharks developed effective immune responses upon green fluorescent protein (GFP), near-infrared fluorescent protein iRFP713, and Freund’s adjuvant immunization revealed by elevated lymphocyte counts and antigen specific IgNAR. Before and after immunization, the complementarity determining region 3 (CDR3) of IgNAR were the major determinant of IgNAR diversity revealed by 400-bp deep sequencing. To prove that bamboo sharks could produce high-affinity IgNAR, we isolated anti-GFP and anti-iRFP713 vNARs with up to 0.3 and 3.8 nM affinities, respectively, from immunized sharks. Moreover, we constructed biparatopic vNARs with the highest known affinities (20.7 pM) to GFP and validated the functions of anti-GFP vNARs as intrabodies in mammalian cells. Taken together, our study will accelerate the discovery and development of bamboo shark sdAbs for biomedical industry at low cost and easy operation.
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spelling pubmed-86928932021-12-23 Bamboo Shark as a Small Animal Model for Single Domain Antibody Production Wei, Likun Wang, Meiniang Xiang, Haitao Jiang, Yuan Gong, Jinhua Su, Dan Al Azad, M. A. R. Dong, Hongming Feng, Limin Wu, Jiajun Chan, Leo Lai Yang, Naibo Shi, Jiahai Front Bioeng Biotechnol Bioengineering and Biotechnology The development of shark single domain antibodies (sdAbs) is hindered by the high cost and tediousness of large-sized shark farming. Here, we demonstrated white-spotted bamboo sharks (Chiloscyllium plagiosum) being cultivated commercially as a promising small animal model to produce sdAbs. We found that immunoglobulin new antigen receptor (IgNAR) presented in bamboo shark genome, transcriptome, and plasma. Four complete IgNAR clusters including variable domains (vNARs) were discovered in the germline, and the Variable–Joining pair from IgNAR1 cluster was dominant from immune repertoires in blood. Bamboo sharks developed effective immune responses upon green fluorescent protein (GFP), near-infrared fluorescent protein iRFP713, and Freund’s adjuvant immunization revealed by elevated lymphocyte counts and antigen specific IgNAR. Before and after immunization, the complementarity determining region 3 (CDR3) of IgNAR were the major determinant of IgNAR diversity revealed by 400-bp deep sequencing. To prove that bamboo sharks could produce high-affinity IgNAR, we isolated anti-GFP and anti-iRFP713 vNARs with up to 0.3 and 3.8 nM affinities, respectively, from immunized sharks. Moreover, we constructed biparatopic vNARs with the highest known affinities (20.7 pM) to GFP and validated the functions of anti-GFP vNARs as intrabodies in mammalian cells. Taken together, our study will accelerate the discovery and development of bamboo shark sdAbs for biomedical industry at low cost and easy operation. Frontiers Media S.A. 2021-12-08 /pmc/articles/PMC8692893/ /pubmed/34957081 http://dx.doi.org/10.3389/fbioe.2021.792111 Text en Copyright © 2021 Wei, Wang, Xiang, Jiang, Gong, Su, Al Azad, Dong, Feng, Wu, Chan, Yang and Shi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Wei, Likun
Wang, Meiniang
Xiang, Haitao
Jiang, Yuan
Gong, Jinhua
Su, Dan
Al Azad, M. A. R.
Dong, Hongming
Feng, Limin
Wu, Jiajun
Chan, Leo Lai
Yang, Naibo
Shi, Jiahai
Bamboo Shark as a Small Animal Model for Single Domain Antibody Production
title Bamboo Shark as a Small Animal Model for Single Domain Antibody Production
title_full Bamboo Shark as a Small Animal Model for Single Domain Antibody Production
title_fullStr Bamboo Shark as a Small Animal Model for Single Domain Antibody Production
title_full_unstemmed Bamboo Shark as a Small Animal Model for Single Domain Antibody Production
title_short Bamboo Shark as a Small Animal Model for Single Domain Antibody Production
title_sort bamboo shark as a small animal model for single domain antibody production
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8692893/
https://www.ncbi.nlm.nih.gov/pubmed/34957081
http://dx.doi.org/10.3389/fbioe.2021.792111
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