Antibody Binding Epitope Mapping (AbMap) of Hundred Antibodies in a Single Run

Antibodies play essential roles in both diagnostics and therapeutics. Epitope mapping is essential to understand how an antibody works and to protect intellectual property. Given the millions of antibodies for which epitope information is lacking, there is a need for high-throughput epitope mapping....

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Veröffentlicht in:Molecular & cellular proteomics 2021-01, Vol.20, p.100059-100059, Article 100059
Hauptverfasser: Qi, Huan, Ma, Mingliang, Hu, Chuansheng, Xu, Zhao-wei, Wu, Fan-lin, Wang, Nan, Lai, Dan-yun, Li, Yang, Zhang, Hainan, Jiang, He-wei, Meng, Qing-feng, Guo, Shujuan, Kang, Yani, Zhao, Xiaodong, Li, Hua, Tao, Sheng-ce
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container_title Molecular & cellular proteomics
container_volume 20
creator Qi, Huan
Ma, Mingliang
Hu, Chuansheng
Xu, Zhao-wei
Wu, Fan-lin
Wang, Nan
Lai, Dan-yun
Li, Yang
Zhang, Hainan
Jiang, He-wei
Meng, Qing-feng
Guo, Shujuan
Kang, Yani
Zhao, Xiaodong
Li, Hua
Tao, Sheng-ce
description Antibodies play essential roles in both diagnostics and therapeutics. Epitope mapping is essential to understand how an antibody works and to protect intellectual property. Given the millions of antibodies for which epitope information is lacking, there is a need for high-throughput epitope mapping. To address this, we developed a strategy, Antibody binding epitope Mapping (AbMap), by combining a phage displayed peptide library with next-generation sequencing. Using AbMap, profiles of the peptides bound by 202 antibodies were determined in a single test, and linear epitopes were identified for >50% of the antibodies. Using spike protein (S1 and S2)-enriched antibodies from the convalescent serum of one COVID-19 patient as the input, both linear and potentially conformational epitopes of spike protein specific antibodies were identified. We defined peptide-binding profile of an antibody as the binding capacity (BiC). Conceptually, the BiC could serve as a systematic and functional descriptor of any antibody. Requiring at least one order of magnitude less time and money to map linear epitopes than traditional technologies, AbMap allows for high-throughput epitope mapping and creates many possibilities. [Display omitted] •The first technology enables epitope mapping of 200 antibodies in a single run.•Applications of antibodies, not for original antigens, were further exploited.•The epitopes of antibodies in one COVID-19 patient were identified.•The BiC is a new systematic and functional character of antibody. In this study, we developed a strategy, Antibody binding epitope Mapping (AbMap), by combining a phage displayed peptide library with next-generation sequencing. By AbMap, epitopes of 202 antibodies were determined in a single test. Also, the epitopes of spike protein-specific antibodies from convalescent serum of one COVID-19 patient were identified. We defined the profile of the binding peptides of an antibody as binding capacity (BiC), conceptually, BiC could serve as a systematic and functional character for any antibody.
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Epitope mapping is essential to understand how an antibody works and to protect intellectual property. Given the millions of antibodies for which epitope information is lacking, there is a need for high-throughput epitope mapping. To address this, we developed a strategy, Antibody binding epitope Mapping (AbMap), by combining a phage displayed peptide library with next-generation sequencing. Using AbMap, profiles of the peptides bound by 202 antibodies were determined in a single test, and linear epitopes were identified for &gt;50% of the antibodies. Using spike protein (S1 and S2)-enriched antibodies from the convalescent serum of one COVID-19 patient as the input, both linear and potentially conformational epitopes of spike protein specific antibodies were identified. We defined peptide-binding profile of an antibody as the binding capacity (BiC). Conceptually, the BiC could serve as a systematic and functional descriptor of any antibody. Requiring at least one order of magnitude less time and money to map linear epitopes than traditional technologies, AbMap allows for high-throughput epitope mapping and creates many possibilities. [Display omitted] •The first technology enables epitope mapping of 200 antibodies in a single run.•Applications of antibodies, not for original antigens, were further exploited.•The epitopes of antibodies in one COVID-19 patient were identified.•The BiC is a new systematic and functional character of antibody. In this study, we developed a strategy, Antibody binding epitope Mapping (AbMap), by combining a phage displayed peptide library with next-generation sequencing. By AbMap, epitopes of 202 antibodies were determined in a single test. Also, the epitopes of spike protein-specific antibodies from convalescent serum of one COVID-19 patient were identified. We defined the profile of the binding peptides of an antibody as binding capacity (BiC), conceptually, BiC could serve as a systematic and functional character for any antibody.</description><identifier>ISSN: 1535-9476</identifier><identifier>EISSN: 1535-9484</identifier><identifier>DOI: 10.1074/mcp.RA120.002314</identifier><identifier>PMID: 33109704</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Antibodies, Monoclonal - immunology ; Antibodies, Monoclonal - metabolism ; Antibodies, Viral - metabolism ; COVID-19 ; COVID-19 - immunology ; Enzyme-Linked Immunosorbent Assay ; epitope mapping ; Epitope Mapping - methods ; Epitopes - metabolism ; Escherichia coli Proteins - immunology ; High-Throughput Nucleotide Sequencing ; Humans ; Immune Sera - blood ; Immune Sera - immunology ; next-generation sequencing ; Peptide Library ; phage display ; random peptide library ; Spike Glycoprotein, Coronavirus - immunology</subject><ispartof>Molecular &amp; cellular proteomics, 2021-01, Vol.20, p.100059-100059, Article 100059</ispartof><rights>2021</rights><rights>Copyright © 2021. 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Epitope mapping is essential to understand how an antibody works and to protect intellectual property. Given the millions of antibodies for which epitope information is lacking, there is a need for high-throughput epitope mapping. To address this, we developed a strategy, Antibody binding epitope Mapping (AbMap), by combining a phage displayed peptide library with next-generation sequencing. Using AbMap, profiles of the peptides bound by 202 antibodies were determined in a single test, and linear epitopes were identified for &gt;50% of the antibodies. Using spike protein (S1 and S2)-enriched antibodies from the convalescent serum of one COVID-19 patient as the input, both linear and potentially conformational epitopes of spike protein specific antibodies were identified. We defined peptide-binding profile of an antibody as the binding capacity (BiC). Conceptually, the BiC could serve as a systematic and functional descriptor of any antibody. Requiring at least one order of magnitude less time and money to map linear epitopes than traditional technologies, AbMap allows for high-throughput epitope mapping and creates many possibilities. [Display omitted] •The first technology enables epitope mapping of 200 antibodies in a single run.•Applications of antibodies, not for original antigens, were further exploited.•The epitopes of antibodies in one COVID-19 patient were identified.•The BiC is a new systematic and functional character of antibody. In this study, we developed a strategy, Antibody binding epitope Mapping (AbMap), by combining a phage displayed peptide library with next-generation sequencing. By AbMap, epitopes of 202 antibodies were determined in a single test. Also, the epitopes of spike protein-specific antibodies from convalescent serum of one COVID-19 patient were identified. 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Epitope mapping is essential to understand how an antibody works and to protect intellectual property. Given the millions of antibodies for which epitope information is lacking, there is a need for high-throughput epitope mapping. To address this, we developed a strategy, Antibody binding epitope Mapping (AbMap), by combining a phage displayed peptide library with next-generation sequencing. Using AbMap, profiles of the peptides bound by 202 antibodies were determined in a single test, and linear epitopes were identified for &gt;50% of the antibodies. Using spike protein (S1 and S2)-enriched antibodies from the convalescent serum of one COVID-19 patient as the input, both linear and potentially conformational epitopes of spike protein specific antibodies were identified. We defined peptide-binding profile of an antibody as the binding capacity (BiC). Conceptually, the BiC could serve as a systematic and functional descriptor of any antibody. Requiring at least one order of magnitude less time and money to map linear epitopes than traditional technologies, AbMap allows for high-throughput epitope mapping and creates many possibilities. [Display omitted] •The first technology enables epitope mapping of 200 antibodies in a single run.•Applications of antibodies, not for original antigens, were further exploited.•The epitopes of antibodies in one COVID-19 patient were identified.•The BiC is a new systematic and functional character of antibody. In this study, we developed a strategy, Antibody binding epitope Mapping (AbMap), by combining a phage displayed peptide library with next-generation sequencing. By AbMap, epitopes of 202 antibodies were determined in a single test. Also, the epitopes of spike protein-specific antibodies from convalescent serum of one COVID-19 patient were identified. 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subjects Antibodies, Monoclonal - immunology
Antibodies, Monoclonal - metabolism
Antibodies, Viral - metabolism
COVID-19
COVID-19 - immunology
Enzyme-Linked Immunosorbent Assay
epitope mapping
Epitope Mapping - methods
Epitopes - metabolism
Escherichia coli Proteins - immunology
High-Throughput Nucleotide Sequencing
Humans
Immune Sera - blood
Immune Sera - immunology
next-generation sequencing
Peptide Library
phage display
random peptide library
Spike Glycoprotein, Coronavirus - immunology
title Antibody Binding Epitope Mapping (AbMap) of Hundred Antibodies in a Single Run
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