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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2012
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.
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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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