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Generation and Characterization of a Novel Recombinant Antibody Against 15-Ketocholestane Isolated by Phage-Display
The employment of monoclonal antibodies (Mabs) to identify disease-associated biomarkers in clinical samples represents the underlying principle for many diagnostic tests. To date, these have been principally developed for protein targets with few reported applications for lipids due to their hydrop...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344257/ https://www.ncbi.nlm.nih.gov/pubmed/22606021 http://dx.doi.org/10.3390/ijms13044937 |
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author | Islam, Md. Omedul Lim, Yan Ting Chan, Conrad En Zuo Cazenave-Gassiot, Amaury Croxford, J. Ludovic Wenk, Markus R. Macary, Paul A. Hanson, Brendon J. |
author_facet | Islam, Md. Omedul Lim, Yan Ting Chan, Conrad En Zuo Cazenave-Gassiot, Amaury Croxford, J. Ludovic Wenk, Markus R. Macary, Paul A. Hanson, Brendon J. |
author_sort | Islam, Md. Omedul |
collection | PubMed |
description | The employment of monoclonal antibodies (Mabs) to identify disease-associated biomarkers in clinical samples represents the underlying principle for many diagnostic tests. To date, these have been principally developed for protein targets with few reported applications for lipids due to their hydrophobicity and poor immunogenicity. Oxysterols represent a family of lipids implicated in diverse human diseases where Mab-based detection assays could have a profound effect on their utility as clinical biomarkers. These are usually identified in patients’ samples by mass- spectrometry based approaches. Here, we describe an antibody phage-library based screening methodology for generating a recombinant monoclonal antibody (RAb) targeting the oxysterol-15-ketocholestane (15-KA), a lipid implicated in multiple sclerosis and Autoimmune Encephalomyelitis (EAE). The antibody is highly specific for 15-KA and shows little or no binding activity for other closely related oxysterols. We employ RAb2E9 to address the controversy over whether 15-KA is a true biomarker for MS/EAE and show that 15-KA is undetectable in serum taken from mice with EAE using antibody based detection methodologies; a finding confirmed by mass-spectrometry analysis. This study demonstrates the technical feasibility of using phage display to isolate highly specific antibodies against poorly immunogenic, small molecule lipids. |
format | Online Article Text |
id | pubmed-3344257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-33442572012-05-17 Generation and Characterization of a Novel Recombinant Antibody Against 15-Ketocholestane Isolated by Phage-Display Islam, Md. Omedul Lim, Yan Ting Chan, Conrad En Zuo Cazenave-Gassiot, Amaury Croxford, J. Ludovic Wenk, Markus R. Macary, Paul A. Hanson, Brendon J. Int J Mol Sci Article The employment of monoclonal antibodies (Mabs) to identify disease-associated biomarkers in clinical samples represents the underlying principle for many diagnostic tests. To date, these have been principally developed for protein targets with few reported applications for lipids due to their hydrophobicity and poor immunogenicity. Oxysterols represent a family of lipids implicated in diverse human diseases where Mab-based detection assays could have a profound effect on their utility as clinical biomarkers. These are usually identified in patients’ samples by mass- spectrometry based approaches. Here, we describe an antibody phage-library based screening methodology for generating a recombinant monoclonal antibody (RAb) targeting the oxysterol-15-ketocholestane (15-KA), a lipid implicated in multiple sclerosis and Autoimmune Encephalomyelitis (EAE). The antibody is highly specific for 15-KA and shows little or no binding activity for other closely related oxysterols. We employ RAb2E9 to address the controversy over whether 15-KA is a true biomarker for MS/EAE and show that 15-KA is undetectable in serum taken from mice with EAE using antibody based detection methodologies; a finding confirmed by mass-spectrometry analysis. This study demonstrates the technical feasibility of using phage display to isolate highly specific antibodies against poorly immunogenic, small molecule lipids. Molecular Diversity Preservation International (MDPI) 2012-04-19 /pmc/articles/PMC3344257/ /pubmed/22606021 http://dx.doi.org/10.3390/ijms13044937 Text en © 2012 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Islam, Md. Omedul Lim, Yan Ting Chan, Conrad En Zuo Cazenave-Gassiot, Amaury Croxford, J. Ludovic Wenk, Markus R. Macary, Paul A. Hanson, Brendon J. Generation and Characterization of a Novel Recombinant Antibody Against 15-Ketocholestane Isolated by Phage-Display |
title | Generation and Characterization of a Novel Recombinant Antibody Against 15-Ketocholestane Isolated by Phage-Display |
title_full | Generation and Characterization of a Novel Recombinant Antibody Against 15-Ketocholestane Isolated by Phage-Display |
title_fullStr | Generation and Characterization of a Novel Recombinant Antibody Against 15-Ketocholestane Isolated by Phage-Display |
title_full_unstemmed | Generation and Characterization of a Novel Recombinant Antibody Against 15-Ketocholestane Isolated by Phage-Display |
title_short | Generation and Characterization of a Novel Recombinant Antibody Against 15-Ketocholestane Isolated by Phage-Display |
title_sort | generation and characterization of a novel recombinant antibody against 15-ketocholestane isolated by phage-display |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344257/ https://www.ncbi.nlm.nih.gov/pubmed/22606021 http://dx.doi.org/10.3390/ijms13044937 |
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