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In Vitro Affinity Maturation of Nanobodies against Mpox Virus A29 Protein Based on Computer-Aided Design
Mpox virus (MPXV), the most pathogenic zoonotic orthopoxvirus, caused worldwide concern during the SARS-CoV-2 epidemic. Growing evidence suggests that the MPXV surface protein A29 could be a specific diagnostic marker for immunological detection. In this study, a fully synthetic phage display librar...
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/PMC10574621/ https://www.ncbi.nlm.nih.gov/pubmed/37836685 http://dx.doi.org/10.3390/molecules28196838 |
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author | Yu, Haiyang Mao, Guanchao Pei, Zhipeng Cen, Jinfeng Meng, Wenqi Wang, Yunqin Zhang, Shanshan Li, Songling Xu, Qingqiang Sun, Mingxue Xiao, Kai |
author_facet | Yu, Haiyang Mao, Guanchao Pei, Zhipeng Cen, Jinfeng Meng, Wenqi Wang, Yunqin Zhang, Shanshan Li, Songling Xu, Qingqiang Sun, Mingxue Xiao, Kai |
author_sort | Yu, Haiyang |
collection | PubMed |
description | Mpox virus (MPXV), the most pathogenic zoonotic orthopoxvirus, caused worldwide concern during the SARS-CoV-2 epidemic. Growing evidence suggests that the MPXV surface protein A29 could be a specific diagnostic marker for immunological detection. In this study, a fully synthetic phage display library was screened, revealing two nanobodies (A1 and H8) that specifically recognize A29. Subsequently, an in vitro affinity maturation strategy based on computer-aided design was proposed by building and docking the A29 and A1 three-dimensional structures. Ligand-receptor binding and molecular dynamics simulations were performed to predict binding modes and key residues. Three mutant antibodies were predicted using the platform, increasing the affinity by approximately 10-fold compared with the parental form. These results will facilitate the application of computers in antibody optimization and reduce the cost of antibody development; moreover, the predicted antibodies provide a reference for establishing an immunological response against MPXV. |
format | Online Article Text |
id | pubmed-10574621 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105746212023-10-14 In Vitro Affinity Maturation of Nanobodies against Mpox Virus A29 Protein Based on Computer-Aided Design Yu, Haiyang Mao, Guanchao Pei, Zhipeng Cen, Jinfeng Meng, Wenqi Wang, Yunqin Zhang, Shanshan Li, Songling Xu, Qingqiang Sun, Mingxue Xiao, Kai Molecules Article Mpox virus (MPXV), the most pathogenic zoonotic orthopoxvirus, caused worldwide concern during the SARS-CoV-2 epidemic. Growing evidence suggests that the MPXV surface protein A29 could be a specific diagnostic marker for immunological detection. In this study, a fully synthetic phage display library was screened, revealing two nanobodies (A1 and H8) that specifically recognize A29. Subsequently, an in vitro affinity maturation strategy based on computer-aided design was proposed by building and docking the A29 and A1 three-dimensional structures. Ligand-receptor binding and molecular dynamics simulations were performed to predict binding modes and key residues. Three mutant antibodies were predicted using the platform, increasing the affinity by approximately 10-fold compared with the parental form. These results will facilitate the application of computers in antibody optimization and reduce the cost of antibody development; moreover, the predicted antibodies provide a reference for establishing an immunological response against MPXV. MDPI 2023-09-28 /pmc/articles/PMC10574621/ /pubmed/37836685 http://dx.doi.org/10.3390/molecules28196838 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 Yu, Haiyang Mao, Guanchao Pei, Zhipeng Cen, Jinfeng Meng, Wenqi Wang, Yunqin Zhang, Shanshan Li, Songling Xu, Qingqiang Sun, Mingxue Xiao, Kai In Vitro Affinity Maturation of Nanobodies against Mpox Virus A29 Protein Based on Computer-Aided Design |
title | In Vitro Affinity Maturation of Nanobodies against Mpox Virus A29 Protein Based on Computer-Aided Design |
title_full | In Vitro Affinity Maturation of Nanobodies against Mpox Virus A29 Protein Based on Computer-Aided Design |
title_fullStr | In Vitro Affinity Maturation of Nanobodies against Mpox Virus A29 Protein Based on Computer-Aided Design |
title_full_unstemmed | In Vitro Affinity Maturation of Nanobodies against Mpox Virus A29 Protein Based on Computer-Aided Design |
title_short | In Vitro Affinity Maturation of Nanobodies against Mpox Virus A29 Protein Based on Computer-Aided Design |
title_sort | in vitro affinity maturation of nanobodies against mpox virus a29 protein based on computer-aided design |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10574621/ https://www.ncbi.nlm.nih.gov/pubmed/37836685 http://dx.doi.org/10.3390/molecules28196838 |
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