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Broad specificity of immune helminth scFv library to identify monoclonal antibodies targeting Strongyloides
Antibodies have different chemical properties capable of targeting a diverse nature of antigens. Traditionally, immune antibody libraries are perceived to be disease-specific with a skewed repertoire. The complexity during the generation of a combinatorial antibody library allows for a skewed but di...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7843650/ https://www.ncbi.nlm.nih.gov/pubmed/33510342 http://dx.doi.org/10.1038/s41598-021-82125-3 |
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author | Rahumatullah, Anizah Balachandra, Dinesh Noordin, Rahmah Baharudeen, Zamrina Lim, Yee Ying Choong, Yee Siew Lim, Theam Soon |
author_facet | Rahumatullah, Anizah Balachandra, Dinesh Noordin, Rahmah Baharudeen, Zamrina Lim, Yee Ying Choong, Yee Siew Lim, Theam Soon |
author_sort | Rahumatullah, Anizah |
collection | PubMed |
description | Antibodies have different chemical properties capable of targeting a diverse nature of antigens. Traditionally, immune antibody libraries are perceived to be disease-specific with a skewed repertoire. The complexity during the generation of a combinatorial antibody library allows for a skewed but diverse repertoire to be generated. Strongyloides stercoralis is a parasite that causes strongyloidiasis, a potentially life-threatening disease with a complex diagnosis that impedes effective control and treatment of the disease. This study describes the isolation of monoclonal antibodies against S. stercoralis NIE recombinant protein using an immune antibody phage display library derived from lymphatic filaria-infected individuals. The isolated antibody clones showed both lambda and kappa light chains gene usage, with diverse amino acid distributions. Structural analysis showed that electropositivity and the interface area could determine the binding affinity of the clones with NIE. The successful identification of S. stercoralis antibodies from the filarial immune library highlights the breadth of antibody gene diversification in an immune antibody library that can be applied for closely related infections. |
format | Online Article Text |
id | pubmed-7843650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78436502021-01-29 Broad specificity of immune helminth scFv library to identify monoclonal antibodies targeting Strongyloides Rahumatullah, Anizah Balachandra, Dinesh Noordin, Rahmah Baharudeen, Zamrina Lim, Yee Ying Choong, Yee Siew Lim, Theam Soon Sci Rep Article Antibodies have different chemical properties capable of targeting a diverse nature of antigens. Traditionally, immune antibody libraries are perceived to be disease-specific with a skewed repertoire. The complexity during the generation of a combinatorial antibody library allows for a skewed but diverse repertoire to be generated. Strongyloides stercoralis is a parasite that causes strongyloidiasis, a potentially life-threatening disease with a complex diagnosis that impedes effective control and treatment of the disease. This study describes the isolation of monoclonal antibodies against S. stercoralis NIE recombinant protein using an immune antibody phage display library derived from lymphatic filaria-infected individuals. The isolated antibody clones showed both lambda and kappa light chains gene usage, with diverse amino acid distributions. Structural analysis showed that electropositivity and the interface area could determine the binding affinity of the clones with NIE. The successful identification of S. stercoralis antibodies from the filarial immune library highlights the breadth of antibody gene diversification in an immune antibody library that can be applied for closely related infections. Nature Publishing Group UK 2021-01-28 /pmc/articles/PMC7843650/ /pubmed/33510342 http://dx.doi.org/10.1038/s41598-021-82125-3 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Rahumatullah, Anizah Balachandra, Dinesh Noordin, Rahmah Baharudeen, Zamrina Lim, Yee Ying Choong, Yee Siew Lim, Theam Soon Broad specificity of immune helminth scFv library to identify monoclonal antibodies targeting Strongyloides |
title | Broad specificity of immune helminth scFv library to identify monoclonal antibodies targeting Strongyloides |
title_full | Broad specificity of immune helminth scFv library to identify monoclonal antibodies targeting Strongyloides |
title_fullStr | Broad specificity of immune helminth scFv library to identify monoclonal antibodies targeting Strongyloides |
title_full_unstemmed | Broad specificity of immune helminth scFv library to identify monoclonal antibodies targeting Strongyloides |
title_short | Broad specificity of immune helminth scFv library to identify monoclonal antibodies targeting Strongyloides |
title_sort | broad specificity of immune helminth scfv library to identify monoclonal antibodies targeting strongyloides |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7843650/ https://www.ncbi.nlm.nih.gov/pubmed/33510342 http://dx.doi.org/10.1038/s41598-021-82125-3 |
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